ENCODE hype? From now on I'll just reply: #oniontest

Posted 5 September 2012 by

The science media exploded today with the claim from the ENCODE project that 80% of the genome is "functional". The creationists are already beside themselves with joy. And the problem cannot be blamed on the science media, although I wish they were quicker to exercise independent skepticism -- the 80% claim is right there in the abstract of the Nature article. However, skepticism has arisen spontaneously from all over the scientific blogosphere, facebook, and twitter. You see, most of us scientists know that (a) ENCODE is using an extremely liberal and dubious definition of "function", basically meaning "some detectable chemical activity". People have pointed out that randomly generated DNA sequences would often be "functional" on this definition. (b) All the evidence for relative nonfunctionality which has been known for decades is still there and hasn't really changed -- lack of conservation, onion test, etc. But I'm beginning to think that certain parts of molecular biology and bioinformatics are populated with people who are very smart, but who got through school with a lot of detailed technical training but without enough broad training in basic comparative biology. Anyway, I'd write more, but I'm jammed and Ryan Gregory has said everything I would say, except better: http://www.genomicron.evolverzone.com/2012/09/a-slightly-different-response-to-todays-encode-hype/ See also Larry Moran: http://sandwalk.blogspot.com/2012/09/encode-leader-says-that-80-of-our.html, especially the rather wry comments. Hashtag: #oniontest

111 Comments

ksplawn · 5 September 2012

Yeah, it would have been better for everybody if the ENCODE team had dubbed their findings "potentially active" or something along those lines instead of hijacking a term that is used differently in the same field.

ogremk5 · 5 September 2012

The creationists couldn't care less what the actual result is, as long as SOME scientists said something else.

If creationists actually wanted to say anything about this, then they should have made a prediction long ago. The prediction needed to include an estimate of this perceived functionality and why their notions say so. They also need to explain why it is discriminatory between creationism (including ID) and science.

Just because someone is 'wrong' (for some value of wrong) about something, that doesn't mean that the opposing side is right. Creationists NEVER EVER learn that simple truth. Which means that they are doomed to failure every single time.

Failure? Sorry. To fail, one must try. Creationists (including IDiots) never ever try.

DS · 5 September 2012

Well, this just means that twenty percent of the genome isn't functional, by even the most liberal definition of the term. So creationists lose again. Now why would they claim victory if the facts are actually still against them? What? ... Oh. Never mind.

Reed A. Cartwright · 5 September 2012

GIGO

Robert Byers · 5 September 2012

The interesting comment here to me is saying lots of SMART people go through education in "science" subjects but unless they concentrate their thinking on a particular subject then their opinion is not as relevant as those who do concentrate/study.
Creationists always complain the "scientific community" agreeing by vote with evolution counts as intellectual understanding behind the merits of the contention.
In fact only those who study "evolution' etc can claim to be scientists in the subject and as authority that creationists must respect and address.
Not the others and no points for family support.

DavidK · 5 September 2012

When the DNA structure was first being defined and analyzed, it was asserted by someone that it mostly non-functional, an assertion based solely on initial and preliminary investigations. That view has changed over time as more and more research continues into DNA/RNA structures. However, that perspective is changing due to increased scrutiny and research of DNA as well as other biological experimentation. But so what. Even if DNA is 100% functional, so to speak, that has no implications regarding it as having been 'designed' by some supernatural deity. There is no credible link to be made, only empty creationist assertions to that effect.

Joe Felsenstein · 5 September 2012

If 100% of the genome, or 80% of the genome, is not "junk" then we just have to adjust to that. But these seem unlikely to be true. The most general definition of non-junk DNA I can think of is DNA whose base sequence (at a site) makes a noticeable difference to the organism's fitness. And noticeable does not just mean noticeable by us in a lab, it means big enough to affect the outcome of evolution. Population genetic theory shows that this means that the selection coefficient (the fractional difference in fitness) is bigger than ±1/(4N), where N is the effective population size. That is a small number but not zero.

Just because something is transcribed into RNA does not necessarily mean that it makes that much difference in fitness. Is that the criterion they are using?

Joe Felsenstein · 5 September 2012

I should add some comments on why creationists are upset about there being any noticeable amount of junk DNA. I say "creationists" because it is creationism, not specifically ID arguments, that is at issue.

Creationists don't like junk DNA because:

1. It is something that can't be explained by a Designer, unless she is someone who is trying to confuse us or make us think that the organisms arose with common descent. If it is junk, then it is difficult to conceive of any functional purpose except perhaps as a message to us. And a confusing one at that.

2. Similarities in junk DNA are evidence for common descent. They can be explained by it. If you try to explain those similarities by "common design" you run afoul of point 1 -- what could be the point of that design?

Creationist and ID debaters are quick to disparage "bad design" arguments. They usually argue that we cannot judge what is good and bad design in the mind of the Designer. But after taking that lofty position, they run into junk DNA and don't like it because that would be bad design. It seems to me that they can't have it both ways (but they of course do anyway).

They often argue that the absence of junk DNA is a prediction of Intelligent Design. I think that when they argue that, people should ask them exactly where this prediction was made. William Dembski's arguments do not address the issue. Nor do Michael Behe's. So where did this prediction take place? Is it a theological prediction rather than a scientific one?

They also often argue that "Darwinism" needs junk DNA to be present. Actually evolutionary biologists did not predict it originally, though they wondered in the 1950s how there could be that much DNA in the genome if it all was under natural selection. Ohno's arguments in 1969 made the case, and eventually the reality of substantial amounts of junk DNA was accepted. You won't find arguments favoring the existence of junk DNA in the pre-1969 papers of Fisher, Wright, and Haldane, and no mention of it in pre-1969 writings of founders of the Modern Synthesis such as Mayr, Simpson, Dobzhansky, Huxley, and Stebbins. (I wonder, though, whether H. J. Muller won't be discovered to have suspected its existence).

Joe Felsenstein · 5 September 2012

DavidK said: When the DNA structure was first being defined and analyzed, it was asserted by someone that it mostly non-functional, an assertion based solely on initial and preliminary investigations. ...
That's news to me. Who? Have you got a reference? Maybe as a mention in a textbook?

bbennett1968 · 6 September 2012

The interesting comment here to me is saying lots of SMART people go through education in “science” subjects but unless they concentrate their thinking on a particular subject then their opinion is not as relevant as those who do concentrate/study
There there's you, who knows pretty much nothing about any subject, and won't ever shut up despite your throughly demonstrated incompetence in biology, geology, general science, history, theology, law, spelling, grammar and style. Your poorly-formatted and un-proofread ramblings do an excellent job of showing the abject ignorance and nonsense of your pet idea and its supporters every day, and for this I thank you.

harold · 6 September 2012

Joe Felsenstein said: If 100% of the genome, or 80% of the genome, is not "junk" then we just have to adjust to that. But these seem unlikely to be true. The most general definition of non-junk DNA I can think of is DNA whose base sequence (at a site) makes a noticeable difference to the organism's fitness. And noticeable does not just mean noticeable by us in a lab, it means big enough to affect the outcome of evolution. Population genetic theory shows that this means that the selection coefficient (the fractional difference in fitness) is bigger than ±1/(4N), where N is the effective population size. That is a small number but not zero. Just because something is transcribed into RNA does not necessarily mean that it makes that much difference in fitness. Is that the criterion they are using?
First of all, just creationists idiotically "celebrating" because an obvious piece of evidence against creationism has been in some way discussed (the authors here are obviously not arguing for creationism nor against the concept of non-functional DNA). It's also worth noting that is that "junk" is a relative and subjective term. I do agree that it's the best widely accepted general term for a certain broad set of types of DNA sequences found in eukaryotic genomes. Obviously, there are things like LINES, SINES, ERVs, pseudogenes, and so on, which we can explain the origins of, which were clearly not directly adaptive for humans at their time of origin. By human values, "junk" in a highly reasonable sense. But lots of DNA that doesn't code for a protein or miRNA is at least expressed, usually due to promiscuous expression. Genes can be used no matter how they got there. An ERV protein has been co-opted by some but not all mammals (including humans) for an important role in placental biology. If it's DNA it can theoretically be expressed, either if it becomes associated with appropriate regulatory elements, or even at a low level without that. And if it's DNA it can be transposed. And if those things happen it can hypothetically "do" something. And then, and not just with creationists, but also between scientists, the semantic question of whether or not it is still "junk" gets rolling. It may do something bad, in which case most would agree it's still junk, but it may do something neutral or even beneficial. Bacteria really don't have "junk" DNA to any serious extent. It's a eukaryotic phenomenon. Yet this is not evidence that bacteria were magically created. I understand that the existence of "junk" DNA is taken as an argument for "bad design", and I agree that it is, but I never liked the whole "bad design" approach anyway. It involves applying subjective human values to a hypothetical creator deity. I prefer to note that if the "designer" did create all species instantaneously, she made it look exactly like evolution to me. The types of DNA we call junk certainly provide evidence for evolution, and still will if we begin calling them "platinum executive plan DNA". Where's the positive evidence, not silly selective denial of evidence against it, positive evidence for

eric · 6 September 2012

Robert Byers said: The interesting comment here to me is saying lots of SMART people go through education in "science" subjects but unless they concentrate their thinking on a particular subject then their opinion is not as relevant as those who do concentrate/study.
Robert, nobody is claiming the ENCODE scientists' conclusions are wrong. They are claiming that how the ENCODE scientists define 'functional' does not match up with how you, I, and most other people would define 'functional.' I'm sure the work will be relevant and useful to future biological research. The issue is whether it supports the vernacular conclusion you (or I, or most people) might draw from the headline. The commenters are saying: it doesn't.

eric · 6 September 2012

Oops, forgot my ending comment:

Robert, this is a squabble about how to present results; over what a set of results means. It is not a squabble over whether the results are good science.

DS · 6 September 2012

Robert Byers said: The interesting comment here to me is saying lots of SMART people go through education in "science" subjects but unless they concentrate their thinking on a particular subject then their opinion is not as relevant as those who do concentrate/study. Creationists always complain the "scientific community" agreeing by vote with evolution counts as intellectual understanding behind the merits of the contention. In fact only those who study "evolution' etc can claim to be scientists in the subject and as authority that creationists must respect and address. Not the others and no points for family support.
So why don't you Byers? Why do you have no respect at all for any of the real professional biologists who study evolution for a living? Why are you so willing to dismiss all of the evidence and all of the conclusions drawn by the real experts simply because you don't want to believe it? Do you do this in other fields as well? Why should anyone care what you think when you can't even be bothered to spell Dna correctly? Keep it up dude. You are the best argument against creationism ever invented. Now, are you willing to admit that at least twenty percent of your genome is "junk"? Are you willing to admit that no intelligent designer would do such a thing? Are you willing to admit that this is exactly what one would expect if the human genome evolved over millions of years? Are you willing to listen to the experts who you obviously respect so much? Or are you just gonna put your hands over your ears and scream "intelligent design" at the top of your lungs whether it makes any sense or not? That's what I thought.

veritea · 6 September 2012

FYI... From Discovery Magazine:

And what's in the remaining 20 percent? Possibly not junk either, according to Ewan Birney, the project's Lead Analysis Coordinator and self-described "cat-herder-in-chief". He explains that ENCODE only (!) looked at 147 types of cells, and the human body has a few thousand. A given part of the genome might control a gene in one cell type, but not others. If every cell is included, functions may emerge for the phantom proportion. "It's likely that 80 percent will go to 100 percent," says Birney. "We don't really have any large chunks of redundant DNA. This metaphor of junk isn't that useful."

DavidK · 6 September 2012

Joe Felsenstein said:
DavidK said: When the DNA structure was first being defined and analyzed, it was asserted by someone that it mostly non-functional, an assertion based solely on initial and preliminary investigations. ...
That's news to me. Who? Have you got a reference? Maybe as a mention in a textbook?
See the wikipedia article at http://en.wikipedia.org/wiki/Junk_DNA under the subsection Junk DNA

benjamin.cutler · 6 September 2012

More on the problem with how these results were reported. Unfortunately, due to bad reporting and the wording of the press release, the actual results (which give us a better understanding of the biochemistry going on inside the cell) are being overshadowed by all the hype.

Nick Matzke · 6 September 2012

Wow. Watch the Twitter-splosion: https://twitter.com/mbeisen

https://me.yahoo.com/a/JxVN0eQFqtmgoY7wC1cZM44ET_iAanxHQmLgYgX_Zhn8#57cad · 6 September 2012

Just for argument's sake, let's suppose that IDiocy makes any real predictions (how can they when the "designer" is neither identified nor characterized?) and that this actually fits their "prediction".

OK, the real non-teleological evolutionary prediction is the slavishly derivative nature of life, whether horizontally where this is known to occur, or vertically in the case of most vertebrates and many other eukaryotes. How does ID account for life being fraught with evidence of such evolutionary limitations, which all known species of designer (us, essentially) readily transcend?

That's right, it doesn't, it just pretends that it doesn't matter.

Any evidence of forethought, planning, complete novelty, or rationality in life? No? Then there is no evidence for design in life, and (see above) endless evidence of the evolution of life.

Glen Davidson

eric · 6 September 2012

veritea - a completly unsurprising and unremarkable prediction given their uber-broad definition of 'functional.'

Yeah, based on their defition of functional, 100% of the genome (or close to it) probably IS functional.

Why not? Is there any reason to believe that rearranging the ATCG subunits will make a biologically active polymer into a non-biologically active one?

SensuousCurmudgeon · 6 September 2012

There's still the fact that the amoeba has a genome about ten times larger than ours. Is it all functional? And there's a Japanese flower with a genome 50 times larger than ours. There must be some junk in there somewhere.

SonOfHastur · 6 September 2012

SensuousCurmudgeon said: There's still the fact that the amoeba has a genome about ten times larger than ours. Is it all functional? And there's a Japanese flower with a genome 50 times larger than ours. There must be some junk in there somewhere.
That's something I find interesting. If the position of ID finds "complexity" to be so important, and (by their apparent definition) man must be more "complex" than any other animal, then the obvious conclusion would be that man would have a larger genome than any other organism. Conversely, since a creature that is essentially a little blob of goo has a larger genome than we do, maybe you could say that our complexity reduces the amount of genome necessary for us to exist. Of course since you can then point to organisms (of varying levels of apparent complexity) that have smaller genomes than man. In other words, comparing genetic complexity grants a perfect example of what you would expect from a process of evolution: A sloppy, chaotic mess. More on the topic of the OP: If IDers want to insist that all DNA is functional (which not all stand by) then there is a "victory" requirement that they commonly seem to ignore: Proving 100% DNA functionality means proving that every gene in a human is meaningful and functional, as well as every gene in an amoeba, every gene in a radish, every gene in a diplodocus, every gene in a strange warthog-like creature that lives on a planet 2,000 light years away, etc., etc.,etc. Put simply, in order to claim that there is NO non-functional DNA, you must be able to show that ALL genetic material that ever existed has function.

eric · 6 September 2012

SonOfHastur said: That's something I find interesting. If the position of ID finds "complexity" to be so important, and (by their apparent definition) man must be more "complex" than any other animal, then the obvious conclusion would be that man would have a larger genome than any other organism.
Another obvious (and amusing) ID conclusion from the onion test is that what modern science considers different varieties of onions must actually be different "kinds" and separately created. Because in the genetic difference between some onion varieties is not just bigger than the genetic diffence between humans and chimps, the difference is bigger than the entire human genome. ;)

ogremk5 · 6 September 2012

eric said:
SonOfHastur said: That's something I find interesting. If the position of ID finds "complexity" to be so important, and (by their apparent definition) man must be more "complex" than any other animal, then the obvious conclusion would be that man would have a larger genome than any other organism.
Another obvious (and amusing) ID conclusion from the onion test is that what modern science considers different varieties of onions must actually be different "kinds" and separately created. Because in the genetic difference between some onion varieties is not just bigger than the genetic diffence between humans and chimps, the difference is bigger than the entire human genome. ;)
That's very cool. Similar to dogs. The morphological differences between dog species is larger than the morphological difference between all other carnivores combined.

Joe Felsenstein · 6 September 2012

DavidK said:
Joe Felsenstein said:
DavidK said: When the DNA structure was first being defined and analyzed, it was asserted by someone that it mostly non-functional, an assertion based solely on initial and preliminary investigations. ...
That's news to me. Who? Have you got a reference? Maybe as a mention in a textbook?
See the wikipedia article at http://en.wikipedia.org/wiki/Junk_DNA under the subsection Junk DNA
OK, that's Susumu Ohno in 1972, nearly 20 years after Watson and Crick. I was thinking you were talking about the period right after 1953. The only hint in the 1950s of an issue of whether the DNA was all functional was the "c value paradox" that amounts of DNA did not correlate with complexity of organisms.

https://me.yahoo.com/a/j5i6uksLusgEaijZZYDXbBvVNwGLR34JYQj_JIeOO3eKfg--#35e25 · 6 September 2012

It would be nice if the ENCODE people had at least mentioned the c-value paradox. Yet another example of biologists who concentrate unduly on model organisms forgetting the value of comparative studies. I wonder how they would respond on the question. Do other species (e.g. onions) have lots of junk, and it just happens that humans have very little? How would they deal with fugu? I doubt we'll be seeing any answers to those questions.

https://me.yahoo.com/a/j5i6uksLusgEaijZZYDXbBvVNwGLR34JYQj_JIeOO3eKfg--#35e25 · 6 September 2012

And can anyone tell me how I stop being a masked panda and start being me instead? John H.

John Harshman · 6 September 2012

Never mind. I figured out a workaround

Flint · 6 September 2012

As far as I can tell, EVEN IF we should discover some function, either active or passive (like alignment) for 100% of the base pairs in our DNA, this would still be consistent with evolutionary processes. And if we should establish beyond reasonable doubt that some hefty percent does absolutely nothing, that's consistent with evolutionary processes as well. And of course ANY finding whatsoever is consistent with an unknown designer doing unpredictable things for unknowable purposes.

So where's the problem here?

glipsnort · 6 September 2012

I think there would be significant evolutionary problem if 80% of the genome really were functional(*). If 80% were functional, then every human would be born with ~60 new deleterious mutations. There has been a low-key debate for a long time about whether a deleterious mutation rate of ~3 per birth would impose too high a genetic load on humans; 60 strikes me as extremely unlikely.

(*) Where "functional" has any definition recognizable by competent speakers of English, i.e. not the idiotic definition used in the ENCODE papers.

Joe Felsenstein · 6 September 2012

Yes, the mutational load issue is serious. This was one of the reasons population geneticists accepted that much of the genome must consist of bases whose mutation would not reduce fitness. If "functional" means that a change in the sequence changes fitness, your argument is a strong one.

For a more detailed technical discussion, see my free ebook Theoretical Evolutionary Genetics, particularly section III.6 and the preceding material in Chapter III.

fusilier · 7 September 2012

Joe Felsenstein wrote:
For a more detailed technical discussion, see my free ebook Theoretical Evolutionary Genetics, particularly section III.6 and the preceding material in Chapter III.
Thank you for this resource. fusilier James 2:24

Rolf · 7 September 2012

Flint said: As far as I can tell, EVEN IF we should discover some function, either active or passive (like alignment) for 100% of the base pairs in our DNA, this would still be consistent with evolutionary processes. And if we should establish beyond reasonable doubt that some hefty percent does absolutely nothing, that's consistent with evolutionary processes as well. And of course ANY finding whatsoever is consistent with an unknown designer doing unpredictable things for unknowable purposes. So where's the problem here?
The problem is the creationists, they jump on everything in the hope that it may be a valid argument for creationism. You can always do that without any knowledge or understanding of the subject. What a comfortable position! I continuously have to think and make an effort to learn and understand. But I gladly do it, I've always lived that way.

eric · 7 September 2012

Flint said: As far as I can tell, EVEN IF we should discover some function, either active or passive (like alignment) for 100% of the base pairs in our DNA, this would still be consistent with evolutionary processes. And if we should establish beyond reasonable doubt that some hefty percent does absolutely nothing, that's consistent with evolutionary processes as well. And of course ANY finding whatsoever is consistent with an unknown designer doing unpredictable things for unknowable purposes. So where's the problem here?
Just a quibble (and this is IMO, IANAB), but an 'absolute zero' would be difficult to explain via evolution, because for that to occur every nonfunctional mutation would have to be fatal in the womb. The more nonfatal, nonfunctional mutations that are theoretically possible, the more probable it is that someone's going to be carrying one. Hovewever, the amount of nunfunctional DNA could certainly be very low without much theoretical problem. That would be consistent with currently understood evolution + hypothesis that replicating unnecessary strings has a significant survival or reproductive cost to the organism. In such a situation, the (carriers of) nonfunctional strings would get weeded out pretty quickly.

eric · 7 September 2012

Follow on:

Think of it like an equilibrium reaction, or water flowing into a bucket that has a hole in the bottom. The flow into the bucket represents the rate of nonfunctional mutation. The flow out represents the cost to the organism. The water level is % population which has nonfunctinal genetic strings. If the hole in the bottom is big compared to the inflow, you get little or no water in the bucket. If the hole is small compared to the inflow, you get a full bucket (which = everyone has such strings). You can also get situations where the bucket remains partially full, if the inflow and hole size are similar enough that an equal flow state is reached.

We seem to be in an overflowing bucket world, but evolution is perfectly consistent with a partially full bucket world or even one-drop-going-through-the-bucket world. However, evolution is not consistent with a world in which the tap is turned off. At an absolute minimum, assuming the bucket is nothing but a cylinder open on both ends, evolution predicts that we should still be able to take a snapshot of a drop dropping through the bucket. Which = finding some still-developing individual with a nonfunctional mutation, even if they never make it to breeding age.

apokryltaros · 7 September 2012

Rolf said:
Flint said: As far as I can tell, EVEN IF we should discover some function, either active or passive (like alignment) for 100% of the base pairs in our DNA, this would still be consistent with evolutionary processes. And if we should establish beyond reasonable doubt that some hefty percent does absolutely nothing, that's consistent with evolutionary processes as well. And of course ANY finding whatsoever is consistent with an unknown designer doing unpredictable things for unknowable purposes. So where's the problem here?
The problem is the creationists, they jump on everything in the hope that it may be a valid argument for creationism. You can always do that without any knowledge or understanding of the subject. What a comfortable position! I continuously have to think and make an effort to learn and understand. But I gladly do it, I've always lived that way.
It is a comfortable position until you step back and notice that no one of worth takes your diving into the world's largest haystack for imaginary needles in your quest for a magic bullet seriously.

ogremk5 · 7 September 2012

About the mutational load, I know you all know this, but there are plenty of mutation events that don't actually make changes to how the resulting protein forms.

Even if there's a change in the amino acids, as long as it's not an active site and the change is between similar aminos (both are hydrophobic for example), then a mutation can be totally invisible until you sequence the genome.

Joe Felsenstein · 7 September 2012

eric said:
Flint said: As far as I can tell, EVEN IF we should discover some function, either active or passive (like alignment) for 100% of the base pairs in our DNA, this would still be consistent with evolutionary processes. And if we should establish beyond reasonable doubt that some hefty percent does absolutely nothing, that's consistent with evolutionary processes as well. And of course ANY finding whatsoever is consistent with an unknown designer doing unpredictable things for unknowable purposes. So where's the problem here?
Just a quibble (and this is IMO, IANAB), but an 'absolute zero' would be difficult to explain via evolution, because for that to occur every nonfunctional mutation would have to be fatal in the womb.
A fitness of zero (a selection coefficient of -1) would be possible either by having the individual survive but be sterile, or having it die before reproduction begins. It does not need to die in the womb.
The more nonfatal, nonfunctional mutations that are theoretically possible, the more probable it is that someone's going to be carrying one.
The mutational load argument is subtler than that. Even if a mutation has a relatively weak selection against it, it will ultimately be eliminated from the population (as long as it is not so weakly selected that it is effectively a neutral mutation). In the long run for every deleterious mutant that occurs, one is eliminated by natural selection. If mutants at one site have selection coefficient -0.1, and mutants at another have selection coefficient -0.001, the latter ones will rise to an equilibrium frequency 100 times bigger than the former. The result will be that the net reduction of fitness at both sites will be equal. (For recessive mutants that are only eliminated when homozygous, there is s reduction of the mutational load, but only by a factor of 2). This argument was discovered by J.B.S. Haldane in 1939 and independently by H. J. Muller in 1950. eric's "hole in the bucket" analogy in his next comment is a reasonable analogy: the net outflow from the bucket always ends up balancing the inflow, whatever the size of the hole.
Hovewever, the amount of n[o]nfunctional DNA could certainly be very low without much theoretical problem. That would be consistent with currently understood evolution + hypothesis that replicating unnecessary strings has a significant survival or reproductive cost to the organism. In such a situation, the (carriers of) nonfunctional strings would get weeded out pretty quickly.
The cost of replicating DNA does not appear to be that great. A nasty nearly-legless salamander called the Congo Eel or Blind Eel (Amphiuma) is the DNA champion among vertebrates, for example, having 25 times as much DNA as humans do. They survive just fine and seem unworried by the cost of replicating their DNA. And I very much doubt that they have 25 times as many regulatory sites in their DNA as we do. Similarly for Nick's onions.

eric · 7 September 2012

Joe Felsenstein said:
eric said: Just a quibble (and this is IMO, IANAB), but an 'absolute zero' would be difficult to explain via evolution, because for that to occur every nonfunctional mutation would have to be fatal in the womb.
A fitness of zero (a selection coefficient of -1) would be possible either by having the individual survive but be sterile, or having it die before reproduction begins. It does not need to die in the womb.
Ah, I agree - I think I was unclear in what my zero refers to. By "utter zero" I meant "no member of the population is ever found to have any such mutation." That would be somewhat inconsistent with how we understand evolution. Even if such a mutation results in sterility, you'd still (probabilistically) expect any given generation to have a nonzero number of such members. Of course, if such a mutation results in sterility, its hard to see how it fits the category of 'nonfunctional' any more. :) Almost by definition/tautology, the sorts of mutations we are talking about cannot have an immediate and strong developmental influence on the organism. If they do, they are functional.
The cost of replicating DNA does not appear to be that great.
If it wasn't clear, I agree. The empirical evidence seems to indicate that we live in a 'full-bucket world,' where the hole is much smaller than the inflow.

Flint · 7 September 2012

Interesting discussion. I felt that the equilibrium idea made sense. But I'm aware that some genomes have almost no non-functional DNA (in the sense that it contributes nothing to fitness), and yet those organisms do just fine. So near-100% functionality (the creationist dream) isn't impossible.

Joe Felsenstein · 7 September 2012

eric said: ... Of course, if such a mutation results in sterility, its hard to see how it fits the category of 'nonfunctional' any more. :) Almost by definition/tautology, the sorts of mutations we are talking about cannot have an immediate and strong developmental influence on the organism. If they do, they are functional.
This is backwards. The point of the mutation load argument was not to establish that the sites that have deleterious mutations are nonfunctional. It was to point out the consequences of being functional.
The cost of replicating DNA does not appear to be that great.
If it wasn't clear, I agree. The empirical evidence seems to indicate that we live in a 'full-bucket world,' where the hole is much smaller than the inflow.
The bucket analogy is fine for selected sites, and they differ in sizes of the hole. I'm not sure we want to try to get the analogy to work for buckets that might overflow.

Joe Felsenstein · 7 September 2012

Flint said: Interesting discussion. I felt that the equilibrium idea made sense. But I'm aware that some genomes have almost no non-functional DNA (in the sense that it contributes nothing to fitness), and yet those organisms do just fine. So near-100% functionality (the creationist dream) isn't impossible.
It is possible. It is just that in practice we do have (lots of) processes putting junk into the genome, and natural selection is not so efficient as to remove it immediately.

Joe Felsenstein · 7 September 2012

A correction: It turns out that the "congo eel" Amphiuma is not the genome size champion among vertebrates. That crown is worn by another salamander, Necturus lewisi, the Neuse River Waterdog, which has 120 picograms of DNA per genome, fully 34 times as much as humans have.

Nick Matzke's onions have only 6 times as much DNA as humans.

Interestingly, both Amphiuma and Necturus lewisi live in the southeastern U.S., where they are surrounded by creationists who deny the existence of most of their genomes.

co · 7 September 2012

ogremk5 said: Similar to dogs. The morphological differences between dog species is larger than the morphological difference between all other carnivores combined.
Really? I admit I'm not up to the latest claims, but how could this *possibly* be true, even if we only include mammals in the "carnivores" category? Are shrews carnivores? Whales are. Admitting other, non-mammal carnivores includes things like fish and spiders.

Henry J · 7 September 2012

http://tolweb.org/Carnivora/15971

The order Carnivora includes dogs, cats, bears, raccoons, weasels, mongooses, hyenas, seals, walruses, etc.

So yeah, the ones in that list other than dogs seem to me to have more variety than dogs do by themselves.

BTW, whales are in the order Cetacean, shrews are in order Insectivora.

ksplawn · 7 September 2012

Unless something has changed in the last few years, the largest measured vertebrate genome belongs to the marbled lungfish (Australia's Protopterus aethiopicus, @ 133pg). Necturus lewisi is definitely up there, though.

As I found out a recently, good old daphnia (D. pulex, model organism and popular fish snack) has some interesting things going on in its DNA. Its genome is tiny by one metric, with just 200 million base pairs of DNA vs. humans @ 3+ billion. But it has ~30,000 protein coding genes vs. our ~20,000. It has a lot of duplicate genes and accumulated gene variants.

This might be due to its reproductive cycle. When conditions are favorable, they spawn only females parthenogenetically. When conditions take a turn for the worse, it triggers the parthenogenetic birth of males for sexual reproduction. So in fat times they simply clone themselves, but when times get lean they make the switch to sexual reproduction, with the resulting gene recombination helping to shuffle the population's genes. Combined with fast generation times, it may be a recipe for rapid evolutionary changes in response to the environment. Beneficial mutations can be generated quickly, spread around, and preserved (hence the large number of genes compared to humans).

A little more involved than the onion test, but it brings up another facet of evolution that most denialists don't want to deal with: the benefit of genetic diversity leading to improved chances of accumulating and exploiting beneficial mutations. Beneficial mutations are something many anti-evolutionists claim shouldn't even exist, or would be too rare to make a difference. So not only does the tiny, simple water flea have a larger number of genes than us, it also has a system to better utilize those rare beneficial mutations.

ogremk5 · 7 September 2012

OK, I may have exaggerated slightly. Here's the paper I referred to http://flywings.org.uk/PDF%20files/AmNat2010.pdf and a quote from the abstract:
The amount of shape variation among domestic dogs far exceeds that in wild species, and it is comparable to the disparity throughout the Carnivora. The greatest shape distances between dog breeds clearly surpass the maximum divergence between species in the Carnivora.

John Harshman · 7 September 2012

ogremk5 said: OK, I may have exaggerated slightly. Here's the paper I referred to http://flywings.org.uk/PDF%20files/AmNat2010.pdf and a quote from the abstract:
The amount of shape variation among domestic dogs far exceeds that in wild species, and it is comparable to the disparity throughout the Carnivora. The greatest shape distances between dog breeds clearly surpass the maximum divergence between species in the Carnivora.
That makes more sense once you realize that they're talking strictly about skull shape, which you might have noted.
Henry J: BTW, whales are in the order Cetacean, shrews are in order Insectivora.
Once, that was true. Now it's Artiodactyla and Lipotyphla (or sometimes Eulipotyphla), respectively.

Henry J · 7 September 2012

Well shazbot. The TOL's page on the clade Eutheria ( http://tolweb.org/Eutheria/15997 ) has a note on it that says it hasn't been updated this millennium.

It shows Cetacea in parallel with Artiodacyla, but has parallel lines instead of a solid bar leading into the later, which I think means there was some question about the tree structure at that time.

That page didn't mention Lipotyphla, but Wiki describes it as mostly a renaming of Insectivora, but with some rearrangements of the tree.

Joe Felsenstein · 7 September 2012

ksplawn said: Unless something has changed in the last few years, the largest measured vertebrate genome belongs to the marbled lungfish (Australia's Protopterus aethiopicus, @ 133pg). Necturus lewisi is definitely up there, though. ...
Thanks, I stand corrected. Let's modify my statement to be that Necturus lewisi is the champion among tetrapods.

John Harshman · 7 September 2012

Henry J said: It shows Cetacea in parallel with Artiodacyla, but has parallel lines instead of a solid bar leading into the later, which I think means there was some question about the tree structure at that time.
No, what it means is that Artiodactyla is paraphyletic. I believe if you click on the branch in question you will get a brief explanation.

SteveP. · 7 September 2012

No wonder design deniers are in a rut. They put credence in the silly onion test. What compels them to assume genome size is proportional to its complexity? Complexity lies elsewhere, duh. At least guys like Shapiro understand this and want to take biology in a more interesting and productive direction.

apokryltaros · 7 September 2012

SteveP. said: No wonder design deniers are in a rut. They put credence in the silly onion test. What compels them to assume genome size is proportional to its complexity? Complexity lies elsewhere, duh. At least guys like Shapiro understand this and want to take biology in a more interesting and productive direction.
And yet, why is it that science-denying bigots like yourself have done absolutely nothing beyond mocking those who don't mindlessly agree with them? What have Intelligent Design proponents done recently to improve science?

ksplawn · 7 September 2012

SteveP. said: No wonder design deniers are in a rut. They put credence in the silly onion test. What compels them to assume genome size is proportional to its complexity?
That's the point, actually. To a very great extent it's not proportional. But let me ask you, would William Dembski say that a large genome contains more Specified Complex Information than a short one?

Henry J · 7 September 2012

Plus, the genome size comparison is only one of the rather large number of pieces of evidence that fits ToE.

The theory isn't established by any one piece of evidence, but by several patterns observed repeatedly across all of it. (But for some reason, science deniers tend to continually overlook this point, even after it has been repeatedly mentioned.)

apokryltaros · 7 September 2012

ksplawn said:
SteveP. said: No wonder design deniers are in a rut. They put credence in the silly onion test. What compels them to assume genome size is proportional to its complexity?
That's the point, actually. To a very great extent it's not proportional. But let me ask you, would William Dembski say that a large genome contains more Specified Complex Information than a short one?
Would Dembski determine a bluefinned tuna's genome has more Specified Complex Information than that of a fugu pufferfish's genome?

Rolf · 8 September 2012

apokryltaros said:
ksplawn said:
SteveP. said: No wonder design deniers are in a rut. They put credence in the silly onion test. What compels them to assume genome size is proportional to its complexity?
That's the point, actually. To a very great extent it's not proportional. But let me ask you, would William Dembski say that a large genome contains more Specified Complex Information than a short one?
Would Dembski determine a bluefinned tuna's genome has more Specified Complex Information than that of a fugu pufferfish's genome?
I am unable to understand how the concept of CSI might have a meaning wrt evolution and development. The way I understand evo-devo, any part of the genome may be active over and over again by any cell during development. The complexity is not just in the genome, it is also about the way each cell partake in the process of development. A small change in the genome may have significant impact on the result. For example, how can the significance of the same gene(s) being used in different ways by different cells during development be employed in calculating genomic CSI? Asking from my laymans POW; I may have got it all wrong...

J. L. Brown · 8 September 2012

Wow, Steve P. likes to sneer and posture!

While you are here, condescending to tell us that 'Complexity lies elsewhere', perhaps you can define complexity for us? Give us a method anyone can apply to determine the complexity of two organisms? Maybe you could be so good as to walk through this method with a few different (suggested by the readership here) organisms, and show the work, the math, at each step so that folks can follow along & learn from the examples? For all the bluster and frantic hand-waving, design-proponents have failed to do this -- even when given a golden opportunity to do so in Dover.

So here are my predictions:
1} profound silence -- you will refuse to answer by ignoring this question; or,
2} verbal diarrhea -- you will use as many words as possible to avoid answering the question, up to, including, and beyond using already discredited 'reasoning', inventing or changing the meaning of words, claiming that you 'have already answered that' when you never have, using papers which have nothing at all to do with this discussion -- or which outright refute you -- as 'support', shifting the burden of proof or work (the classic 'I cannot possibly make my first tic-tac-toe move until after you have rigorously explained how all possible strategies of all possible games in the universe work! Show your math!' whine) to your opponent, or any of dozens of other sleazy & all-too-common-from-the-design-folks tactics.

If this goes as I expect it will, you will richly deserve yet another 'Please Do Not Feed The Troll' sign hung about your neck.

harold · 8 September 2012

Steve P. said -
No wonder design deniers are in a rut.
But we're not design deniers in the ideological sense. I've told you a hundred times at least that you can convince me if you provide some valid evidence for your position, and some reasonable alternate explanation for all the evidence that strongly favors evolution.
They put credence in the silly onion test. What compels them to assume genome size is proportional to its complexity?
But see, once again, all you do is selectively argue against evidence that argues against your position. You're like a bad defense attorney. You don't present a clear alternate theory. You don't address most of the evidence against your client.
Complexity lies elsewhere, duh.
Define complexity, tell me where it lies, and explain how that's relevant to a denial of such basic processes as mutation, genetic drift, and natural selection. To make your arguments convincing, why don't you go through Joe Felsenstein's book and explain where it's wrong, and where your rigorously defined conception of complexity gives different theoretical results.
Wow, Steve P. likes to sneer and posture!
Because that's an incredibly common defense mechanism.

harold · 8 September 2012

J. L. Brown said: Wow, Steve P. likes to sneer and posture! While you are here, condescending to tell us that 'Complexity lies elsewhere', perhaps you can define complexity for us? Give us a method anyone can apply to determine the complexity of two organisms? Maybe you could be so good as to walk through this method with a few different (suggested by the readership here) organisms, and show the work, the math, at each step so that folks can follow along & learn from the examples? For all the bluster and frantic hand-waving, design-proponents have failed to do this -- even when given a golden opportunity to do so in Dover. So here are my predictions: 1} profound silence -- you will refuse to answer by ignoring this question; or, 2} verbal diarrhea -- you will use as many words as possible to avoid answering the question, up to, including, and beyond using already discredited 'reasoning', inventing or changing the meaning of words, claiming that you 'have already answered that' when you never have, using papers which have nothing at all to do with this discussion -- or which outright refute you -- as 'support', shifting the burden of proof or work (the classic 'I cannot possibly make my first tic-tac-toe move until after you have rigorously explained how all possible strategies of all possible games in the universe work! Show your math!' whine) to your opponent, or any of dozens of other sleazy & all-too-common-from-the-design-folks tactics. If this goes as I expect it will, you will richly deserve yet another 'Please Do Not Feed The Troll' sign hung about your neck.
That is a very good prediction. There is a number "3}", which is likely here, and is also quite common. It's essentially a variant of "1}". Instead of silence, ignore the topic, but keep up a string of immature sneers. It's less sophisticated than silence, because silence allows the old "I could have perfectly refuted your points but I didn't have time" dodge, whereas hanging around and sneering makes it even more clear to even the most sympathetic observer that the individual in question can't logically defend their position. You describe "2}" incredibly well, but that strategy requires a fair investment of time, and at least mild ability to mimic an academic style of English. I note that it is disproportionately used by those who get paid, or hope to get paid, for their creationist output. This category includes people in graduate school.

vhutchison · 8 September 2012

@JoeFelstein: I was about to post a comment on the very large anount of DNA in the large paedomorphic salamanders (Necturus, Cryptobranchus, Amphiuma) when I saw your post. Amphiuma also has some of the largest cells of any vertebrate.

Slightly off topic, but any ideas of why the large amounts of DNA and large cell sizes in these paedomorphs? I have asked this of several 'experts' and have not been able to get possible explanations or suggestions.

ksplawn · 8 September 2012

Rolf said: Would Dembski determine a bluefinned tuna's genome has more Specified Complex Information than that of a fugu pufferfish's genome?
I am unable to understand how the concept of CSI might have a meaning wrt evolution and development. Dembski's idea of specified complexity would have to have meaning before it could be meaningfully applied, so the problem isn't with you. SteveP seems to assume that cdesign proponentsists have something valid to work with, so I wondered how they would apply these concepts to things like the incredibly variable size of genomes even among closely related species; let alone the problem of "simple" organisms having several times as much DNA and 50% more genes compared to us humans.

ksplawn · 8 September 2012

And, of course, I messed up the quotes for that response. Blah.
Rolf said: I am unable to understand how the concept of CSI might have a meaning wrt evolution and development.

https://me.yahoo.com/a/JxVN0eQFqtmgoY7wC1cZM44ET_iAanxHQmLgYgX_Zhn8#57cad · 8 September 2012

One thing that shouldn't be forgotten here is that certain types of "junk DNA" are grist for the evolutionary mill. Duplicated genes, in particular, have given rise to different adaptations, indeed, to gene families. Whole genome duplications are thought by many to have played a role in vertebrate evolution.

As far as evolutionary predictions go, there never was the sort of resolution to say how much junk DNA should remain in genomes. Natural selection tends to either weed it out, or to make some sort of regulatory or other use of it, while transposons, duplications, and other mechanisms tend to produce more.

So evolutionary theory hasn't had much of an opinion on how much DNA should be "junk," rather the estimates have been tentative, and based on empirical data with its apparent limitations. Research continues on "junk DNA" precisely because we haven't known how to interpret the empirical data.

What is hardly in question at all, though, is that really (otherwise) useless duplicated DNA has been important in evolution, although even there the question of the degree of importance has been in contention. It's enough in this "debate" to say that gene duplications have certainly provided evolutionary opportunities to point out that, once again, evolutionary science deals meaningfully with "junk DNA," while ID remains nothing but a pretended default explanation. Of course they'll never acknowledge the role of natural selection in making use of "junk DNA," demanding that magic be credited instead, but that's just pathetic.

Glen Davidson

Joe Felsenstein · 8 September 2012

vhison said: @JoeFelstein: I was about to post a comment on the very ...
I know I just deliberately misspelled your name, but that's OK: you misspelled mine.

harold · 8 September 2012

Glen Davidson said -
As far as evolutionary predictions go, there never was the sort of resolution to say how much junk DNA should remain in genomes.
Bacteria have virtually no junk DNA compared with eukaryotes, and some eukaryotes have fairly little as well. The theory of evolution neither predicts nor requires junk DNA, but offers an explanation for it. However, if there is DNA, it creates a problem for ID/creationism evolution denial, because there is no reason for a deity miraculously creating modern organisms out of thin air to include junk DNA. The "conversation" between ID/creationists and geneticists has nothing to do with any challenge to evolution whatsoever. Rather, modern genetics unintentionally challenges, to put it mildly, ID/creationism. (Unintentionally, because most geneticists and molecular biologists couldn't give a rat's ass about creationism and are merely trying to learn more about molecular genetics, but what they learn inevitably makes creationism seem even stupider.) So the ID/creationists are trying to deny or distort modern genetics. Even if creationists could "win" this argument, and they can't because of LINES, SINES, ERVs, pseudogenes, etc, they'd merely be back to only being as wrong as they already were circa 1965. ID/creationists spend a massive amount of their time denying the obvious evidence against ID/creationism. They used to spend a similar amount of time attacking irrelevant straw man versions of evolution, but most of the straw men were invented by the Gish generation, and with the internet, have been widely discredited. Two things they never do are 1) offer a coherent, testable hypothesis, with predictions, of ID/creationism or 2) offer a reasonable alternate explanation for all of the obvious evidence in favor of biological evolution.

Henry J · 8 September 2012

Rather, modern genetics unintentionally challenges, to put it mildly, ID/creationism.

It certainly does. Modern genetics would have predicted (and generated) the theory of evolution if it wasn't already around before DNA was understood, Darwin or no Darwin. Henry

vhutchison · 8 September 2012

@JoeFelsenstein. Sorry Joe, my bad due to thick thumbs!. I know your correct name quite well. BUT, cam you weigh in on my question?

Joe Felsenstein · 9 September 2012

vhutchison said: @JoeFelsenstein. Sorry Joe, my bad due to thick thumbs!. I know your correct name quite well. BUT, cam you weigh in on my question?
I was about to post a comment on the very large anount of DNA in the large paedomorphic salamanders (Necturus, Cryptobranchus, Amphiuma) when I saw your post. Amphiuma also has some of the largest cells of any vertebrate. Slightly off topic, but any ideas of why the large amounts of DNA and large cell sizes in these paedomorphs? I have asked this of several ‘experts’ and have not been able to get possible explanations or suggestions.
Short answer: I haven't a clue -- your guess is as good as mine. I'm a theoretician, so if you have a question about a term in an equation, I might be able to answer. I'd just add that (as I think you realize) the large cell sizes are probably a result of the large amount of DNA, as that is often observed.

Paul Burnett · 9 September 2012

Joe Felsenstein said: ...the large cell sizes are probably a result of the large amount of DNA...
Is that because more of the salamanders' DNA is non-coding ("junk DNA")?

harold · 9 September 2012

Paul Burnett said:
Joe Felsenstein said: ...the large cell sizes are probably a result of the large amount of DNA...
Is that because more of the salamanders' DNA is non-coding ("junk DNA")?
I find the question extremely interesting as well. It is clear that in some eukaryotic lineages, there is less "junk" DNA. Perhaps this represents direct selection against excess junk DNA in those lineages, or perhaps, because selection against junk DNA is so weak, there is a random distribution of its amount throughout lineages. That's a question that could be studied. For example, if the amount of DNA/genome per some logically defined lineage group was distributed along a normal curve, that might argue that a strong element of randomness exists with regard to amount of DNA per genome. Some lineages might have enzymes that regulate genome size more, but such enzymes might not be strongly selected for or against, but merely passed on, or not, in a random way. This would imply a gradual increase in eukaryotic genome sizes over time(since it would be more likely to lose such a function to gain it), at least until some point at which larger genome actually is selected against, which may be reasonable. On the other hand, other types of distributions might imply selection in some lineages. As for cell size, in mammals (and to some degree in all eukaryotes), cell size varies according to a number of factors: 1) Smaller organisms tend to have slightly smaller versions of the same type of cell, but nowhere near in proportion to the size difference between adults of various species. This makes sense when one considers that even the smallest eukaryotic cells, which occur mainly in single celled algae, are a bit less than 1 micrometer in diameter (a size range where they overlap with bacterial cell size). Likewise, there is clearly an upper limit on cell sizes, so whales and elephants don't have gigantic individual cells in proportion to their size. 2) Function: For example, certain types of neurons are very large, both in terms of nucleus and cytoplasm, in all mammals, easily reaching 100 micrometers, not even counting axons and dendrites, in humans. This is the strongest association with the size of normal cells. Cytoplasmic volume is strongly associated with function. Nuclear volume is to a less extent, but still is. Within the immune system, some but not all types of cells respond to stimulation by going through a phase of more rapid cell cycle with larger nuclear size. The megakaryocytes of the bone marrow, which generate blood platelets, are so named because of their large size. 3) Neoplasm: On average, with many exceptions, malignant cells tend to have larger nuclei, as well as different nuclear features. This does tend to associate with DNA content and DNA abnormalities. 4) Radiation: Exposure to ionizing radiation, usually seen in the context of radiation therapy, can lead to transient presence of very large cells, extremely alarming to the untrained eye. Such changes can be morphologically distinguished from malignancy (*of course ionizing radiation exposure is a risk factor for malignancy later, but it causes short term, non-malignant changes as well*). For example the cells often have both increased nuclear size and a large amount of cytoplasm, which is perfectly possible, but less common, in cancer. There are a variety of other features that allow the distinction as well, although in individual cases, it can be tricky.

harold · 9 September 2012

harold said:
Paul Burnett said:
Joe Felsenstein said: ...the large cell sizes are probably a result of the large amount of DNA...
Is that because more of the salamanders' DNA is non-coding ("junk DNA")?
I find the question extremely interesting as well. It is clear that in some eukaryotic lineages, there is less "junk" DNA. Perhaps this represents direct selection against excess junk DNA in those lineages, or perhaps, because selection against junk DNA is so weak, there is a random distribution of its amount throughout lineages. That's a question that could be studied. For example, if the amount of DNA/genome per some logically defined lineage group was distributed along a normal curve, that might argue that a strong element of randomness exists with regard to amount of DNA per genome. Some lineages might have enzymes that regulate genome size more, but such enzymes might not be strongly selected for or against, but merely passed on, or not, in a random way. This would imply a gradual increase in eukaryotic genome sizes over time(since it would be more likely to lose such a function to gain it), at least until some point at which larger genome actually is selected against, which may be reasonable. On the other hand, other types of distributions might imply selection in some lineages. As for cell size, in mammals (and to some degree in all eukaryotes), cell size varies according to a number of factors: 1) Smaller organisms tend to have slightly smaller versions of the same type of cell, but nowhere near in proportion to the size difference between adults of various species. This makes sense when one considers that even the smallest eukaryotic cells, which occur mainly in single celled algae, are a bit less than 1 micrometer in diameter (a size range where they overlap with bacterial cell size). Likewise, there is clearly an upper limit on cell sizes, so whales and elephants don't have gigantic individual cells in proportion to their size. 2) Function: For example, certain types of neurons are very large, both in terms of nucleus and cytoplasm, in all mammals, easily reaching 100 micrometers, not even counting axons and dendrites, in humans. This is the strongest association with the size of normal cells. Cytoplasmic volume is strongly associated with function. Nuclear volume is to a less extent, but still is. Within the immune system, some but not all types of cells respond to stimulation by going through a phase of more rapid cell cycle with larger nuclear size. The megakaryocytes of the bone marrow, which generate blood platelets, are so named because of their large size. 3) Neoplasm: On average, with many exceptions, malignant cells tend to have larger nuclei, as well as different nuclear features. This does tend to associate with DNA content and DNA abnormalities. 4) Radiation: Exposure to ionizing radiation, usually seen in the context of radiation therapy, can lead to transient presence of very large cells, extremely alarming to the untrained eye. Such changes can be morphologically distinguished from malignancy (*of course ionizing radiation exposure is a risk factor for malignancy later, but it causes short term, non-malignant changes as well*). For example the cells often have both increased nuclear size and a large amount of cytoplasm, which is perfectly possible, but less common, in cancer. There are a variety of other features that allow the distinction as well, although in individual cases, it can be tricky.
I should note that we should strongly differentiate between ploidy (copies of the overall genome, or large parts of it), versus amount of junk DNA per single genome. When malignant cells have a lot of DNA, which can lead to either large, or hyperchromatic (by light microscopy with appropriate stains), nuclei, it is essentially because of high rate of replication and/or excess chromosomes. It is still "more DNA per genome" but clearly has different effects on cell morphology than large amounts of non-replicating junk DNA, most of which can be tightly packaged.

harold · 9 September 2012

harold said:
harold said:
Paul Burnett said:
Joe Felsenstein said: ...the large cell sizes are probably a result of the large amount of DNA...
Is that because more of the salamanders' DNA is non-coding ("junk DNA")?
I find the question extremely interesting as well. It is clear that in some eukaryotic lineages, there is less "junk" DNA. Perhaps this represents direct selection against excess junk DNA in those lineages, or perhaps, because selection against junk DNA is so weak, there is a random distribution of its amount throughout lineages. That's a question that could be studied. For example, if the amount of DNA/genome per some logically defined lineage group was distributed along a normal curve, that might argue that a strong element of randomness exists with regard to amount of DNA per genome. Some lineages might have enzymes that regulate genome size more, but such enzymes might not be strongly selected for or against, but merely passed on, or not, in a random way. This would imply a gradual increase in eukaryotic genome sizes over time(since it would be more likely to lose such a function to gain it), at least until some point at which larger genome actually is selected against, which may be reasonable. On the other hand, other types of distributions might imply selection in some lineages. As for cell size, in mammals (and to some degree in all eukaryotes), cell size varies according to a number of factors: 1) Smaller organisms tend to have slightly smaller versions of the same type of cell, but nowhere near in proportion to the size difference between adults of various species. This makes sense when one considers that even the smallest eukaryotic cells, which occur mainly in single celled algae, are a bit less than 1 micrometer in diameter (a size range where they overlap with bacterial cell size). Likewise, there is clearly an upper limit on cell sizes, so whales and elephants don't have gigantic individual cells in proportion to their size. 2) Function: For example, certain types of neurons are very large, both in terms of nucleus and cytoplasm, in all mammals, easily reaching 100 micrometers, not even counting axons and dendrites, in humans. This is the strongest association with the size of normal cells. Cytoplasmic volume is strongly associated with function. Nuclear volume is to a less extent, but still is. Within the immune system, some but not all types of cells respond to stimulation by going through a phase of more rapid cell cycle with larger nuclear size. The megakaryocytes of the bone marrow, which generate blood platelets, are so named because of their large size. 3) Neoplasm: On average, with many exceptions, malignant cells tend to have larger nuclei, as well as different nuclear features. This does tend to associate with DNA content and DNA abnormalities. 4) Radiation: Exposure to ionizing radiation, usually seen in the context of radiation therapy, can lead to transient presence of very large cells, extremely alarming to the untrained eye. Such changes can be morphologically distinguished from malignancy (*of course ionizing radiation exposure is a risk factor for malignancy later, but it causes short term, non-malignant changes as well*). For example the cells often have both increased nuclear size and a large amount of cytoplasm, which is perfectly possible, but less common, in cancer. There are a variety of other features that allow the distinction as well, although in individual cases, it can be tricky.
I should note that we should strongly differentiate between ploidy (copies of the overall genome, or large parts of it), versus amount of junk DNA per single genome. When malignant cells have a lot of DNA, which can lead to either large, or hyperchromatic (by light microscopy with appropriate stains), nuclei, it is essentially because of high rate of replication and/or excess chromosomes. It is still "more DNA per genome" but clearly has different effects on cell morphology than large amounts of non-replicating junk DNA, most of which can be tightly packaged.
And we should differentiate between high ploidy but normal rate of DNA replication, as in many normal plants, versus excess and abnormal cell division, possibly with related gains in ploidy.

harold · 9 September 2012

For completeness I will also note that existence of very large multinucleated cells, both in the human body and in the case of some very large "single celled organisms" these can sort of be considered multiple cells fused together.

DS · 9 September 2012

Joe Felsenstein said:
vhutchison said: @JoeFelsenstein. Sorry Joe, my bad due to thick thumbs!. I know your correct name quite well. BUT, cam you weigh in on my question?
I was about to post a comment on the very large anount of DNA in the large paedomorphic salamanders (Necturus, Cryptobranchus, Amphiuma) when I saw your post. Amphiuma also has some of the largest cells of any vertebrate. Slightly off topic, but any ideas of why the large amounts of DNA and large cell sizes in these paedomorphs? I have asked this of several ‘experts’ and have not been able to get possible explanations or suggestions.
Short answer: I haven't a clue -- your guess is as good as mine. I'm a theoretician, so if you have a question about a term in an equation, I might be able to answer. I'd just add that (as I think you realize) the large cell sizes are probably a result of the large amount of DNA, as that is often observed.
The correlation between DNA content and cell size is due to a nucleotypic effect, that is an effect of the amount of DNA regardless of sequence or coding function. Cells with more DNA tend to be larger, that is why some plant breeders want to make polyploid strains, so that the individual cells and the entire plant will be larger. The same effect is probably seen in the salamanders. The reason for this effect is not entirely clear, however it may involve the ratio of nuclear to cytoplasmic volume and the number of nuclear pores used to transport molecules in and out of the nucleus. This may also explain the presence of synctial cells and somatic polyploidy for many cell types in multicellular organisms.. The amount of DNA can also affect cell cycle time and thus generation time, since more DNA generally takes longer to replicate. This is most likely the explanation for the lack of "junk" DNA in bacteria and mitochondria.

Joe Felsenstein · 9 September 2012

Most of the explanations of large cell size given above are implausible in the case of the lungfish or the salamanders: they do not have cancer, they are not subject to more radiation than other similar creatures, and the types of cell function that they need are not much different from other vertebrates.

(PS Protopteus aethiopicus is the African lungfish, not the Australian one -- I had wondered about the species name which seems inappropriate for anything Australian!)

As for polyploidy, the number of chromosomes in lungfish is not unusual; they seem to be diploid. However they have lots of transposable elements. One paper assessing this (Metcalfe et al., Molecular Biology and Evolution, 2012) concluded that: "the very large Australian lungfish genome may be the result of a massive amplification of TEs followed by a long period with a very low rate of sequence removal and some ongoing TE activity." (TE = transposable element)

harold · 9 September 2012

Joe Felsenstein said: Most of the explanations of large cell size given above are implausible in the case of the lungfish or the salamanders: they do not have cancer, they are not subject to more radiation than other similar creatures, and the types of cell function that they need are not much different from other vertebrates. (PS Protopteus aethiopicus is the African lungfish, not the Australian one -- I had wondered about the species name which seems inappropriate for anything Australian!) As for polyploidy, the number of chromosomes in lungfish is not unusual; they seem to be diploid. However they have lots of transposable elements. One paper assessing this (Metcalfe et al., Molecular Biology and Evolution, 2012) concluded that: "the very large Australian lungfish genome may be the result of a massive amplification of TEs followed by a long period with a very low rate of sequence removal and some ongoing TE activity." (TE = transposable element)
Perhaps I made my comment unclear by changing topics midstream and expecting the reader to follow. My first paragraph was a speculation about marked differences in DNA content per genome in different lineages (which may be due either to ploidy, amount of junk DNA, or both). After that I addressed the topic cell size, implicitly, with a focus on vertebrates, especially mammals. Nuclear DNA content is one such factor, and may explain features of salamander cells. No-one said that radiation had anything major to do with the DNA content of salamanders, nor that all cells in a salamander are neurons; rather, features that associate with cell size were mentioned. (As it happens, I believe there is some evidence that some "amphibians" have issues with UV radiation, and that might partly have something to do with the DNA content of their cells, maybe it could have been selected for because it provides some kind of chemical or stochastic protection against that. "Amphibians" might have "primitive" terrestrial adaptations, including UV exposure adaptation.) On the topic of cell size DS added -
The correlation between DNA content and cell size is due to a nucleotypic effect, that is an effect of the amount of DNA regardless of sequence or coding function. Cells with more DNA tend to be larger, that is why some plant breeders want to make polyploid strains, so that the individual cells and the entire plant will be larger.
There has to be some sort of similar effect in animal cells as well, of course, because the cytoplasm has to at least be large enough to enclose the nucleus. Likewise, organs need enough cells to function, so larger individual cells has to at least have some association with larger organs, and thus larger overall size. However, in human cells, the N:C ratio (nucleus to cytoplasm ratio) is highly variable. Overall there is a trend of larger cytoplasm with larger nucleus, but it is a very weak trend. Needless to say it is even weaker in cancer cells, which tend to have, with many exceptions, high N:C ratio. Plants have quite different cells, of course - they have cell walls. There may be a stronger correlation between nuclear size and cytoplasm size in plants. Cell cycle phase undoubtedly influences nuclear size and appearance in plants, as it does in animals. Multiple factors contribute to cell size, both nuclear size and cytoplasmic size. Nuclear DNA content can be one such factor, but it is not the only one.

harold · 9 September 2012

For more on mammalian cell size, here's a great reference -

http://www.ncbi.nlm.nih.gov/pubmed/17360590

The largest mammalian genome, in terms of base pairs, does belong to a very large animal, but modern whales and elephants have genomes that are not all that different in size from those of mice and humans (and even this is less than double a mouse genome).

http://news.nationalgeographic.com/news/2008/11/081119-mammoth-DNA_2.html

https://me.yahoo.com/a/JxVN0eQFqtmgoY7wC1cZM44ET_iAanxHQmLgYgX_Zhn8#57cad · 9 September 2012

It's thought that birds benefit from an apparent ancestral dinosaur small genome size (smaller than mammals anyhow), hence smaller cells. Less weight for better flight, presumably better diffusion in and out of cells as well (O2, CO2, etc.). Of course they also have the better lungs, unlike God's Designer's end goal, humans.

For mammals, bats also apparently have relatively smaller genomes, but larger than those of birds I believe.

Glen Davidson

harold · 9 September 2012

https://me.yahoo.com/a/JxVN0eQFqtmgoY7wC1cZM44ET_iAanxHQmLgYgX_Zhn8#57cad said: It's thought that birds benefit from an apparent ancestral dinosaur small genome size (smaller than mammals anyhow), hence smaller cells. Less weight for better flight, presumably better diffusion in and out of cells as well (O2, CO2, etc.). Of course they also have the better lungs, unlike God's Designer's end goal, humans. For mammals, bats also apparently have relatively smaller genomes, but larger than those of birds I believe. Glen Davidson
Yes, there does seem to be correlation between C-value and cell size http://www.sciencedirect.com/science/article/pii/S1079979601904577 (I'm going to trust the abstract, not pay $40.) Of course, the variation in cell size within a given bird or mammal is far greater than the variation in cell size between birds and mammals. The exact same genome can and does direct the differentiation of cell types which can be thousands of times greater in volume than other cells of the same individual organism. In addition, the exact same type of cell can sometimes vary in size according to environmental factors. The contribution of individual cell size to organism size is less clear. It does seem to be a factor in plants. Obviously both birds and mammals vary greatly in size. Within mammals, genomes tend to be about the same size, and some cell types are largely invariant in size across all mammals, while others do vary. The largest known modern mammal genome belongs to a small animal that happens to be a rare tetraploid mammal http://en.wikipedia.org/wiki/Tympanoctomys_barrerae For that matter, the largest known plant genome is in a flowering herb, not in the mighty redwood tree http://www.sciencedaily.com/releases/2010/10/101007120641.htm Thus, while there is no doubt that eukaryotic genome size has some influence on nuclear size, and that nuclear size has some influence cytoplasm size (but probably less influence than cell function), the relationship between genome size and body size seems to be at best very weak. Other factors are clearly important as well, even in plants. We should note that genome size in eukaryotes can reflect any of the following - 1) amount of repetitive "junk" DNA, 2) ploidy of entire genome during quiescent phase of cell cycle, or 3) cell cycle stage. When we talk about genome size in terms of picograms of DNA per genome, we aren't differentiating between these.

ksplawn · 9 September 2012

Joe Felsenstein said: (PS Protopteus aethiopicus is the African lungfish, not the Australian one -- I had wondered about the species name which seems inappropriate for anything Australian!)
D'OH!

Joe Felsenstein · 9 September 2012

Joe Felsenstein said: (PS Protopteus aethiopicus is the African lungfish, ...
Oops, that should be Protopterus.

Nick Matzke · 9 September 2012

The correlation between genome size (c-value) and cell size is well-known (although imperfect) -- well, well-known to people who are familiar with the genome size/c-value literature, but apparently not to the ENCODE project people and many other molbio/genomics types.

The hard part is the explanation. The correlation is there, but the causation could run in either direction. E.g.:

(a) skeletal DNA hypothesis: genome size (regardless of the sequence) controls nuclear volume which allometrically controls cell size. Cell size is under selection, e.g. higher metabolism/more rapid growth requires more surface area/smaller cells. Cell size might also be under selection for e.g. brain complexity -- it may be you can have a more complex set of neural connections if each cell is smaller. Ironically, this would mean that more complex creature = SMALLER genome, which is the opposite of creationist/naive functionalist interpretations.

(b) relaxed selection hypothesis -- organisms that grow more slowly have fewer replication events, longer generation times, and lower population sizes. Thus, selection is weaker in these species, and the cost of junk DNA is lower, often lower than the 1/2N neutral cutoff. Thus, it accumulates without negative effect, but if the lineage moves into a niche where it evolves a higher metabolism and faster growth, mutation events that delete junk start to be selectively advantageous, and the genome size starts to shrink.

Both of these hypotheses have strengths and weaknesses. The people to read are Thomas Cavalier-Smith and T. Ryan Gregory.

Any way you slice it, though, it looks like a lot of the genome is pretty dispensable/lacking any specific function (unless "filler" is a function). I am happy calling this "junk DNA", but even some people highly skeptical of functionalist assumptions don't like the label, because of its emotive qualities. Who wants to study "junk", or tell funding agencies that they want to study "junk"?

Nick Matzke · 9 September 2012

Also, two points that are often missed:

1. People often think that it must be energetically expensive to have a bigger genome. But apparently the energetic cost of DNA replication is tiny compared to the cost of protein expression, etc.

2. The size of the genome is relevant to the speed of genome replication in organisms with a single origin of replication (i.e. prokaryotes), but NOT (at least mostly) in eukaryotes, which have many, many origins of replication.

https://www.google.com/accounts/o8/id?id=AItOawm-WhebH0itIDDTj06EQo2vtiF0BBqF10Q · 10 September 2012

https://me.yahoo.com/a/JxVN0eQFqtmgoY7wC1cZM44ET_iAanxHQmLgYgX_Zhn8#57cad said: It's thought that birds benefit from an apparent ancestral dinosaur small genome size (smaller than mammals anyhow), hence smaller cells. Less weight for better flight, presumably better diffusion in and out of cells as well (O2, CO2, etc.). Of course they also have the better lungs, unlike God's Designer's end goal, humans. For mammals, bats also apparently have relatively smaller genomes, but larger than those of birds I believe. Glen Davidson
This is actually the "Flying DNA Hypothesis". Please note though, that insect flight is aerodynamically completely different from that of bats and birds.

ksplawn · 10 September 2012

A piece just went up on Ars Technica about the writer's frustration with the way the ENCODE team and the media have been crowing about "functional" DNA in their findings. Mostly he seems to be tired of the attention-seeking gimmick that any piece of non-coding DNA that turns out to maybe do something under some conditions is touted as a radical overturning everything we thought we knew about genetics, and how the University press offices and the researchers themselves seem to be more than just complicit in promoting this distortion.

DS · 10 September 2012

Since transposons make up approximately 45% of the human genome, the majority of those being SINEs and LINEs it is virtually impossible for 80% of the human genome to have any functional significance. That's not even counting pseudogenes, inactivated mitochondrial genes, completely nonfunctional introns, tandem repeats, etc. We not only know that a lot of the human genome is worthless junk, we know where it came from. It might make sense to view it as raw material, not eliminated by natural selection, but having the potential to eventually mutate into something useful. It certainly doesn't make any sense at all from any intelligent design stand point. Once again, modern genetic discoveries confirm what Darwin claimed all along, descent with modification is true and it explains new discoveries that Darwin could never have dreamed of.

MichaelJ · 10 September 2012

Henry J said:

Rather, modern genetics unintentionally challenges, to put it mildly, ID/creationism.

It certainly does. Modern genetics would have predicted (and generated) the theory of evolution if it wasn't already around before DNA was understood, Darwin or no Darwin. Henry
I think that the no-junk DNA meme is just a random response from the creationists. They could have easily said that junk DNA shows the generally deterioration of the genome since the Fall. It is unusual for them to take a position like this. Generally, they will be vague about their own position and go "Ha Ha Science was wrong again" every time a discovery is made.

harold · 11 September 2012

I think that the no-junk DNA meme is just a random response from the creationists. They could have easily said that junk DNA shows the generally deterioration of the genome since the Fall.
The reason they don't say that is that the since Edwards a major theme is "plausible deniability" of sectarian content. The Fall can be used to counter any "imperfect design" argument, but creationists who have adopted the ID dodge can't use it.
The correlation between genome size (c-value) and cell size is well-known (although imperfect) – well, well-known to people who are familiar with the genome size/c-value literature, but apparently not to the ENCODE project people and many other molbio/genomics types.
To which I add, solely for completeness, that this is the case, in multicellular organisms, when comparable cells of similar function are compared. A typical animal genome guides the development of specialized cell types from lymphocytes to motor neurons (not even counting multinucleate "cells" formed by fusion), which vary greatly in volume.
Ironically, this would mean that more complex creature = SMALLER genome, which is the opposite of creationist/naive functionalist interpretations.
Of course, it depends on what you mean by "complex". The Kolmogorov complexity of a larger genome is greater than that of a smaller genome, at least in the context of sequencing base pairs, simply because it is larger. An argument could be made that ploidy doesn't really count (because you only have to sequence a haploid genome and then add a byte or few to give the ploidy), but the certain lungfish genomes are unequivocally far more complex than the human genome by standard measure. If repetitive sequence representation could be represented in a compressed way that might also be relevant, but basically, more base pairs per haploid genome would tend to mean more Kolmogorov complexity if sequence is being analyzed. A strong argument could be made that many organisms are more "advanced" than humans in many ways. In fact, a traditional Christian, rather than a post-modern right wing ideologue trying to enforce and deny his own religion at the same time, would accept that as uncontroversial.

Nick Matzke · 11 September 2012

Of course, it depends on what you mean by “complex”. The Kolmogorov complexity of a larger genome is greater than that of a smaller genome, at least in the context of sequencing base pairs, simply because it is larger. An argument could be made that ploidy doesn’t really count (because you only have to sequence a haploid genome and then add a byte or few to give the ploidy), but the certain lungfish genomes are unequivocally far more complex than the human genome by standard measure. If repetitive sequence representation could be represented in a compressed way that might also be relevant, but basically, more base pairs per haploid genome would tend to mean more Kolmogorov complexity if sequence is being analyzed. A strong argument could be made that many organisms are more “advanced” than humans in many ways. In fact, a traditional Christian, rather than a post-modern right wing ideologue trying to enforce and deny his own religion at the same time, would accept that as uncontroversial.
These are good points. I was using a (subjective) definition of complexity of the whole organism, where things which are faster, more active, more predatory, smarter, are "more complex". On this definition, it looks like if anything, less DNA = more "complex". Probably what is really going on is a metabolism interaction with genome size -- the interaction could go in either direction.

Carl Drews · 11 September 2012

harold said: A strong argument could be made that many organisms are more "advanced" than humans in many ways.
The feline philosopher Hobbes (in the comic strip "Calvin and Hobbes") says to the boy Calvin with disdain, "Your fingernails are a joke, you've got no fangs, you can't see at night, your pink hides are ridiculous, your reflexes are nil, and you don't even have tails!" [There's Treasure Everywhere, by Bill Watterson, 1996, page 157]

Richard B. Hoppe · 11 September 2012

T. Ryan Gregory has links to several pieces critical of the ENCODE hype.
ksplawn said: A piece just went up on Ars Technica about the writer's frustration with the way the ENCODE team and the media have been crowing about "functional" DNA in their findings. Mostly he seems to be tired of the attention-seeking gimmick that any piece of non-coding DNA that turns out to maybe do something under some conditions is touted as a radical overturning everything we thought we knew about genetics, and how the University press offices and the researchers themselves seem to be more than just complicit in promoting this distortion.

John · 12 September 2012

James Shapiro has just posted his latest piece of breathtaking inanity over at HuffPo. Not surprisingly, he reminds his readers of the two papers he co-authored with Rick Sternbergy, now of the Dishonesty Institute, which he claims anticipated the ENCODE results. I'm not really qualified to comment further since I don't have a background in molecular biology, but feel free to stop by to chime in:

http://www.huffingtonpost.com/james-a-shapiro/bob-dylan-encode-and-evol_b_1873935.html

IMHO this is but his latest effort in grossly distorting public understanding of science, using this as "evidence" of his proposed "paradigm shift" for biology that will feature his uniquely weird Neo-Lamarckian theory of evolution relying on "Natural Genetic Engineering" and the "cognitive behavior" of cells.

I'm sure some of you will appreciate these observations of Shapiro's, replete in their breathtaking inanity:

In 2005, I published two articles on the functional importance of repetitive DNA with Rick von Sternberg. The major article was entitled "Why repetitive DNA is essential to genome function."

These articles with Rick are important to me (and to this blog) for two reasons. The first is that shortly after we submitted them, Rick became a momentary celebrity of the Intelligent Design movement. Critics have taken my co-authorship with Rick as an excuse for "guilt-by-association" claims that I have some ID or Creationist agenda, an allegation with no basis in anything I have written.

The second reason the two articles with Rick are important is because they were, frankly, prescient, anticipating the recent ENCODE results. Our basic idea was that the genome is a highly sophisticated information storage organelle. Just like electronic data storage devices, the genome must be highly formatted by generic (i.e. repeated) signals that make it possible to access the stored information when and where it will be useful.

John · 14 September 2012

Faye Flam has an excellent overview behind the history of science related to the ENCODE paper as well as what it really tells us about Junk DNA here:

http://www.philly.com/philly/columnists/faye_flam/20120910_Planet_of_the_Apes__What_is_that_big_hunk_of__junk__DNA_up_to__.html

I'd also recommend John Farrell's take over at Forbes, in which he cites Larry Moran extensively:

http://www.forbes.com/sites/johnfarrell/2012/09/07/reports-of-junk-dnas-demise-have-been-greatly-exaggerated/

Finally, I am indebted to Diogenes for stopping by at HuffPo to challenge Shapiro's lies about the ENCODE paper. Hope others will follow suit:

http://www.huffingtonpost.com/james[…]1873935.html

DS · 14 September 2012

John said: James Shapiro has just posted his latest piece of breathtaking inanity over at HuffPo. Not surprisingly, he reminds his readers of the two papers he co-authored with Rick Sternbergy, now of the Dishonesty Institute, which he claims anticipated the ENCODE results. I'm not really qualified to comment further since I don't have a background in molecular biology, but feel free to stop by to chime in: http://www.huffingtonpost.com/james-a-shapiro/bob-dylan-encode-and-evol_b_1873935.html IMHO this is but his latest effort in grossly distorting public understanding of science, using this as "evidence" of his proposed "paradigm shift" for biology that will feature his uniquely weird Neo-Lamarckian theory of evolution relying on "Natural Genetic Engineering" and the "cognitive behavior" of cells. I'm sure some of you will appreciate these observations of Shapiro's, replete in their breathtaking inanity: In 2005, I published two articles on the functional importance of repetitive DNA with Rick von Sternberg. The major article was entitled "Why repetitive DNA is essential to genome function." These articles with Rick are important to me (and to this blog) for two reasons. The first is that shortly after we submitted them, Rick became a momentary celebrity of the Intelligent Design movement. Critics have taken my co-authorship with Rick as an excuse for "guilt-by-association" claims that I have some ID or Creationist agenda, an allegation with no basis in anything I have written. The second reason the two articles with Rick are important is because they were, frankly, prescient, anticipating the recent ENCODE results. Our basic idea was that the genome is a highly sophisticated information storage organelle. Just like electronic data storage devices, the genome must be highly formatted by generic (i.e. repeated) signals that make it possible to access the stored information when and where it will be useful.
That's funny, I don't recall him ever predicting that twenty percent of the human genome would turn out to have no discernable function at all, even given the most relaxed definition of "function" imaginable. The genome is definitely not well organized, or well ordered or intelligently designed, or anything like that. As for transposable elements, most of them do absolutely nothing, unless of course they harm the organism. Most of them could cause harm in the future, that would be their most likely "function". You can't say they might do something useful later unless you are willing to give up the "no beneficial mutations" and "no increase in information" and "no genetic innovation" nonsense. The ENCODE results give absolutely no credence whatsoever to any creationist= scenario. Big surprise. And if you think that it does, just ask yourself, why aren't they the ones who actually performed the research?

TChapman500 · 16 September 2012

Why are you ignoring so much scientific research? Surely hundreds of scientists, 30 papers and 80 testing methods would have caught some sort of error before the finding was published.

Here's my full critique of your article:

http://tcrcreation.blogspot.com/2012/09/junk-dna-theory-overturned.html

DS · 16 September 2012

TChapman500 said: Why are you ignoring so much scientific research? Surely hundreds of scientists, 30 papers and 80 testing methods would have caught some sort of error before the finding was published. Here's my full critique of your article: http://tcrcreation.blogspot.com/2012/09/junk-dna-theory-overturned.html
Why are you ignoring the hundreds of thousands of papers that demonstrate that evolution has occurred? By the way, you are incorrect when you claim that "the creationist prediction that entire genome has a function because it was designed to have a function has been fulfilled". You seem to be ignoring the papers you claim that others are ignoring. Read them again.

apokryltaros · 16 September 2012

DS said:
TChapman500 said: Why are you ignoring so much scientific research? Surely hundreds of scientists, 30 papers and 80 testing methods would have caught some sort of error before the finding was published. Here's my full critique of your article: http://tcrcreation.blogspot.com/2012/09/junk-dna-theory-overturned.html
Why are you ignoring the hundreds of thousands of papers that demonstrate that evolution has occurred?
If not millions of such papers. Then again, why should such papers be allowed to matter if they dare to contradict the sacred Holy Bible?
By the way, you are incorrect when you claim that "the creationist prediction that entire genome has a function because it was designed to have a function has been fulfilled". You seem to be ignoring the papers you claim that others are ignoring. Read them again.
Plus, there is the problem of how creationists merely said that to merely to spite and contradict anything Evolutionary Biologists say. And there is the worse problem of how creationists never actually did anything to discover or to research that "the entire genome has a function because it was designed to have a function" to begin with.

John · 16 September 2012

Larry Moran weighs in on Shapiro's jubilation with the ENCODE papers:

http://sandwalk.blogspot.com/2012/09/james-shapiro-claims-credit-for.html

Steve P. · 16 September 2012

Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him. I see you haven't lost your Klingonese accent. Anyway, why don't you take in another visit to the MMoA. So much design on display. Sooner or later you will hopefully 'stumble' upon a Klingonese translation for design. Btw, here is a new English word you ought to have translated. Biosemiotics. UP over at UD was nice enough to introduce this lovely word. Rolls nicely off the tongue. Whats so funny is how much more science I am learning over at UD and ENV than I am here. A curious thing.
John said: Faye Flam has an excellent overview behind the history of science related to the ENCODE paper as well as what it really tells us about Junk DNA here: http://www.philly.com/philly/columnists/faye_flam/20120910_Planet_of_the_Apes__What_is_that_big_hunk_of__junk__DNA_up_to__.html I'd also recommend John Farrell's take over at Forbes, in which he cites Larry Moran extensively: http://www.forbes.com/sites/johnfarrell/2012/09/07/reports-of-junk-dnas-demise-have-been-greatly-exaggerated/ Finally, I am indebted to Diogenes for stopping by at HuffPo to challenge Shapiro's lies about the ENCODE paper. Hope others will follow suit: http://www.huffingtonpost.com/james[…]1873935.html

Keelyn · 17 September 2012

Steve P. said: Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him.
Too bad you leave out the part of exactly how “Diogenes got his ass handed to him,” by Shapiro. I read the comments and it looks like the typical Shapiro style of dodging the questions by providing non answers. Perhaps you should read the comments a second time. Maybe you should read them a first time, preferably with a little comprehension.
Btw, here is a new English word you ought to have translated. Biosemiotics. UP over at UD was nice enough to introduce this lovely word. Rolls nicely off the tongue.
So does BS.
Whats so funny is how much more science I am learning over at UD and ENV than I am here. A curious thing.
There is nothing curious about it at all. It is totally expected of you. You merrily wave away real evidence and science that is provided to you for free here on Panda’s Thumb in favor of what you dogmatically believe is science on UD and ENV. The joke is still on you, silly.

John · 17 September 2012

Steve Proulx the delusional expatriate American rug merchant residing in Taiwan barfed: Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him. I see you haven't lost your Klingonese accent. Anyway, why don't you take in another visit to the MMoA. So much design on display. Sooner or later you will hopefully 'stumble' upon a Klingonese translation for design.
Actually, Shapiro exhibited typical "Disco Tute" behavior in his exchanges with Diogenes. (As an aside, I've recommended to Shapiro that a better home for his blogging would be ENV anyway, jackass.) As for the Metropolitan Museum of Art, the next time you're in New York City and want to have a "pow wow", we'll meet downstairs in the cafetaria; I'll be sure to have friends from museum security keeping a very, very close eye on you, just to ensure that you don't go apeshit crazy.

DS · 17 September 2012

Steve P. said: Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him. I see you haven't lost your Klingonese accent. Anyway, why don't you take in another visit to the MMoA. So much design on display. Sooner or later you will hopefully 'stumble' upon a Klingonese translation for design. Btw, here is a new English word you ought to have translated. Biosemiotics. UP over at UD was nice enough to introduce this lovely word. Rolls nicely off the tongue. Whats so funny is how much more science I am learning over at UD and ENV than I am here. A curious thing.
That's funny, I completely missed the part where he explained why the intelligent designer put twenty percent junk into the human genome. I also missed the part where he explained the exact insertion points for many of the junk elements and how it is completely consistent with descent with modification and completely inconsistent with common design. See the thing is that until creationists start dealing with the actual evidence instead of just making crap up and attacking straw men, they are not going to get anywhere. Now if Stevie would only learn some real science instead of swilling crap from liars and charlatans, then maybe he would eventually get the idea. UNtil then all of his bluff and bluster ring hollow.

apokryltaros · 17 September 2012

DS said: See the thing is that until creationists start dealing with the actual evidence instead of just making crap up and attacking straw men, they are not going to get anywhere.
Other than a few of them getting richer from swindling the stupid Faithful who have been ordered/conditioned to fork over money whenever a Fraud For Jesus says to.
Now if Stevie would only learn some real science instead of swilling crap from liars and charlatans, then maybe he would eventually get the idea.
SteveP repeatedly demonstrates that he would sooner commit suicide than make an attempt to learn real science instead of swallowing anti-science propaganda crap without hesitation. Hell, SteveP even said that he's far too busy making money hand over fist in the fabric industry in Taiwan than to make an attempt to learn science (even though he hypocritically always makes time to troll here).
Until then all of his bluff and bluster ring hollow.
And the sadder thing is that SteveP remains pitifully unaware of this. But, how can one be aware that one's bluff and bluster is impotent when one is programmed only to insult those who don't share one's mindless hatred of science?

diogeneslamp0 · 18 September 2012

Steve P. said: Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him.
You lying piece of shit! I crushed that drooling moron Shapiro. If you think Shapiro made any good points at all, why don't you copy and paste his best point right here, you pussy? I normally don't tangle with you, Steve, because slapping the mentally handicapped is beneath me. But come on, you pussy, copy and paste Shapiro's best point right here, or else go fuck yourself. Do it right now, you fuckhole. I suggest you re-read Michael White's blog post here. I posted 7-8 comments in which I gave about 2 dozen quotes of ENCODE scientists THEMSELVES admitting that they had not disproved the Junk DNA hypothesis. Why are you disputing what the ENCODE scientists now admit-- that most of the genome is probably still junk? They admitted it, and they admitted that they didn't disprove the Junk DNA hypothesis. HuffPost wouldn't let me tell Shapiro how horrible his blog was-- they ditched my comments. So come get me here, pussy. COME GET ME, PUSSY. I listed about two dozen quotes over there. Why don't you address that, asshole?

diogeneslamp0 · 18 September 2012

Keelyn said:
Steve P. said: Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him.
Too bad you leave out the part of exactly how “Diogenes got his ass handed to him,” by Shapiro. I read the comments and it looks like the typical Shapiro style of dodging the questions by providing non answers. Perhaps you should read the comments a second time. Maybe you should read them a first time, preferably with a little comprehension.
Keelyn, several of the comments I posted at Shapiro's blog, in which I listed quotes from ENCODE scientists admitting they hadn't disproven Junk DNA, were never posted by HuffPost, for whatever reason. I got more and better comments through at Michael White's blog, here. I plan to list them all in my blog. There are many.

John · 20 September 2012

diogeneslamp0 said:
Keelyn said:
Steve P. said: Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him.
Too bad you leave out the part of exactly how “Diogenes got his ass handed to him,” by Shapiro. I read the comments and it looks like the typical Shapiro style of dodging the questions by providing non answers. Perhaps you should read the comments a second time. Maybe you should read them a first time, preferably with a little comprehension.
Keelyn, several of the comments I posted at Shapiro's blog, in which I listed quotes from ENCODE scientists admitting they hadn't disproven Junk DNA, were never posted by HuffPost, for whatever reason. I got more and better comments through at Michael White's blog, here. I plan to list them all in my blog. There are many.
Diogenes, HuffPo thinks there is a genuine "debate" going on between Shapiro, White and the others, and are all too willing to bend over backwards in support of Shapiro and his delusional creationist fans like Wendell Read, who opted to stalk me online and sent me four unsolicited e-mails; three after I told him to stop and that I was going to complain about his behavior to the Huffington Post. (Read is Shapiro's "pet", and as intellectually challenged as Stevie Pee.) As for Shapiro, Diogenes, his latest blog is devoted to you and your critiques: http://www.huffingtonpost.com/james-a-shapiro/further-thoughts-on-the-e_b_1893984.html I invite other long-time PT posters - not Stevie Pee and his fellow drive-by creotards - to stop by and give Shapiro a piece of their minds. Shapiro's problem is that he's a once great scientist who has lost touch with reality, as noted, for example, by his blatant lies regarding Darwin's importance in the history of science and Darwin's understanding of Natural Selection. Shapiro has claimed falasely that Darwin wasn't the only one to think of a credible evolutionary theory, citing as examples, not only Lamarck, but also his grandfather, Erasmus Darwin, as examples. For more worrisome is his insistence that Darwin didn't really understand Natural Selection as well as Wallace did, and that he didn't understand it until he read Wallace's 1858 essay.

Dave Luckett · 20 September 2012

John said: I invite other long-time PT posters - not Stevie Pee and his fellow drive-by creotards - to stop by and give Shapiro a piece of their minds.

I would do so, John, with very great pleasure, but pieces of my mind on the details of evolutionary biology and biochemistry are mere grains of sand. I lurk on threads dealing with those subjects, and keep my mouth shut, because I know so little of them. Let Shapiro make a pronouncement on history, theology or the Bible, and I'm your man.

DS · 20 September 2012

John said: Diogenes, HuffPo thinks there is a genuine "debate" going on between Shapiro, White and the others, and are all too willing to bend over backwards in support of Shapiro and his delusional creationist fans like Wendell Read, who opted to stalk me online and sent me four unsolicited e-mails; three after I told him to stop and that I was going to complain about his behavior to the Huffington Post. (Read is Shapiro's "pet", and as intellectually challenged as Stevie Pee.) As for Shapiro, Diogenes, his latest blog is devoted to you and your critiques: http://www.huffingtonpost.com/james-a-shapiro/further-thoughts-on-the-e_b_1893984.html I invite other long-time PT posters - not Stevie Pee and his fellow drive-by creotards - to stop by and give Shapiro a piece of their minds. Shapiro's problem is that he's a once great scientist who has lost touch with reality, as noted, for example, by his blatant lies regarding Darwin's importance in the history of science and Darwin's understanding of Natural Selection. Shapiro has claimed falasely that Darwin wasn't the only one to think of a credible evolutionary theory, citing as examples, not only Lamarck, but also his grandfather, Erasmus Darwin, as examples. For more worrisome is his insistence that Darwin didn't really understand Natural Selection as well as Wallace did, and that he didn't understand it until he read Wallace's 1858 essay.
Thanks for the link John. Unfortunately for Shapiro, his reasoning is tortured at best. He is willing to throw out all that we actually do know in hopes of some day discovering what he hopes to be true. He didn't even deal with the substance of the argument. All he did was make the age old claim that science doesn't provide certainly, therefore I could be proven right in the future. In so doing, he commits the exact same fallacy that he accuses others of. Now where have we seen that kind of behavior before? No wonder the creationists love this guy so much, except maybe for that guy who was trying to claim that Darwin was solely responsible for all of evolutionary biology.

John · 30 September 2012

diogeneslamp0 said:
Keelyn said:
Steve P. said: Challenged? Yes, he did 'challenge' Shapiro. But of course you left out the part where Diogenes got his ass handed to him.
Too bad you leave out the part of exactly how “Diogenes got his ass handed to him,” by Shapiro. I read the comments and it looks like the typical Shapiro style of dodging the questions by providing non answers. Perhaps you should read the comments a second time. Maybe you should read them a first time, preferably with a little comprehension.
Keelyn, several of the comments I posted at Shapiro's blog, in which I listed quotes from ENCODE scientists admitting they hadn't disproven Junk DNA, were never posted by HuffPost, for whatever reason. I got more and better comments through at Michael White's blog, here. I plan to list them all in my blog. There are many.
Diogenes, Shapiro's delusional band of Huffington Post creationist fans have been influencing the moderators to remove your posts as well as some of mine at both Mike White and Shapiro's blogs. I've e-mailed a complaint to them. If you access to Facebook try contacting me there; I'll forward to you the e-mail addresses of those at Huffington Post whom you should contact. I have also alerted Mike White BTW.

John · 30 September 2012

Diogenes, this is somewhat off topic, but James Shapiro demonstrates again just how clueless he is with regards to promoting the teaching of sound basic science like biological evolution and modern evolutionary biology:

http://www.huffingtonpost.com/james-a-shapiro/could-bill-nye-have-done-_b_1919558.html

His condemnation of Bill Nye the Science Guy's recent commentary is yet another example of Shapiro's breathtaking inanity.