The ENCODE project made a big splash a couple of years ago — it is a huge project to not only ask what the sequence of a strand of human DNA was, but to analyzed and annotate and try to figure out what it was doing. One of the very surprising results was that in the sections of DNA analyzed, almost all of the DNA was transcribed into RNA, which sent the creationists and the popular press into unwarranted flutters of excitement that maybe all that junk DNA wasn't junk at all, if enzymes were busy copying it into RNA. This was an erroneous assumption; as John Timmer pointed out, the genome is a noisy place, and coupled with the observations that the transcripts were not evolutionarily conserved, it suggested that these were non-functional transcripts.
Personally, I fall into the "it's all junk" end of the spectrum. If almost all of these sequences are not conserved by evolution, and we haven't found a function for any of them yet, it's hard to see how the "none of it's junk" view can be maintained. There's also an absence of support for the intervening view, again because of a lack of evidence for actual utility. The genomes of closely related species have revealed very few genes added from non-coding DNA, and all of the structural RNA we've found has very specific sequence requirements. The all-junk view, in contrast, is consistent with current data.
Larry Moran was dubious, too — the transcripts could easily by artifactual.
The most widely publicized result is that most of the human genome is transcribed. It might be more correct to say that the ENCODE Project detected RNA's that are either complimentary to much of the human genome or lead to the inference that much of it is transcribed.
This is not news. We've known about this kind of data for 15 years and it's one of the reasons why many scientists over-estimated the number of humans genes in the decade leading up to the publication of the human genome sequence. The importance of the ENCODE project is that a significant fraction of the human genome has been analyzed in detail (1%) and that the group made some serious attempts to find out whether the transcripts really represent functional RNAs.
My initial impression is that they have failed to demonstrate that the rare transcripts of junk DNA are anything other than artifacts or accidents. It's still an open question as far as I'm concerned.
I felt the same way. ENCODE was spitting up an anomalous result, one that didn't fit with any of the other data about junk DNA. I suspected a technical artifact, or an inability of the methods used to properly categorize low frequency accidental transcription in the genome.
Creationists thought it was wonderful. They detest the idea of junk DNA — that the gods would scatter wasteful garbage throughout our precious genome by intent was unthinkable, so any hint that it might actually do something useful is enthusiastically siezed upon as evidence of purposeful design.
Well, score one for the more cautious scientists, and give the creationists another big fat zero (I think the score is somewhere in the neighborhood of a big number requiring scientific notation to be expressed for the scientists, against a nice, clean, simple zero for the creationists). A new paper has come out that analyzes transcripts from the human genome using a new technique, and, uh-oh, it looks like most of the early reports of ubiquitous transcription were wrong.
Here's the author's summary:
The human genome was sequenced a decade ago, but its exact gene composition remains a subject of debate. The number of protein-coding genes is much lower than initially expected, and the number of distinct transcripts is much larger than the number of protein-coding genes. Moreover, the proportion of the genome that is transcribed in any given cell type remains an open question: results from "tiling" microarray analyses suggest that transcription is pervasive and that most of the genome is transcribed, whereas new deep sequencing-based methods suggest that most transcripts originate from known genes. We have addressed this discrepancy by comparing samples from the same tissues using both technologies. Our analyses indicate that RNA sequencing appears more reliable for transcripts with low expression levels, that most transcripts correspond to known genes or are near known genes, and that many transcripts may represent new exons or aberrant products of the transcription process. We also identify several thousand small transcripts that map outside known genes; their sequences are often conserved and are often encoded in regions of open chromatin. We propose that most of these transcripts may be by-products of the activity of enhancers, which associate with promoters as part of their role as long-range gene regulatory sites. Overall, however, we find that most of the genome is not appreciably transcribed.
So, basically, they directly compared the technique used in the ENCODE analysis (the "tiling" microarray analysis) to more modern deep sequencing methods, and found that the old results were mostly artifacts of the protocol. They also directly examined the pool of transcripts produced in specific tissues, and asked what proportion of them came from known genes, and what part came from what has been called the "dark matter" of the genome, or what has usually been called junk DNA. The cell's machinery to transcribe genes turns out to be reasonably precise!
To assess the proportion of unique sequence-mapping reads accounted for by dark matter transcripts in RNA-Seq data, we compared the mapped sequencing data to the combined set of known gene annotations from the three major genome databases (UCSC, NCBI, and ENSEMBL, together referred to here as "annotated" or "known" genes). When considering uniquely mapped reads in all human and mouse samples, the vast majority of reads (88%) originate from exonic regions of known genes. These figures are consistent with previously reported fractions of exonic reads of between 75% and 96% for unique reads, including those of the original studies from which some of the RNA-Seq data in this study were derived. When including introns, as much as 92%-93% of all reads can be accounted for by annotated gene regions. A further 4%-5% of reads map to unannotated genomic regions that can be aligned to spliced ESTs and mRNAs from high-throughput cDNA sequencing efforts, and only 2.2%-2.5% of reads cannot be explained by any of the aforementioned categories.
Furthermore, when they looked at where the mysterious transcripts are coming from, they are most frequently from regions of DNA near known genes, not just out of deep intergenic regions. This also suggests that they're an artifact, like an extended transcription of a gene, or from other possibly regulatory bits, like pasRNA (promoter-associated small RNAs — there's a growing cloud of xxxRNA acronyms growing out there, but while they may be extremely useful, like siRNA, they're still tiny as a fraction of the total genome. Don't look for demolition of the concept of junk DNA here).
There clearly are still mysteries in there — they do identify a few novel transcripts that come up out of the intergenic regions — but they are small and rare, and the fact of their existence does not imply a functional role, since they could simply be byproducts of other processes. The only way to demonstrate that they actually do something will require experiments in genetic perturbation.
The bottom line, though, is the genome is mostly dead, transcriptionally. The junk is still junk.
van Bakel H, Nislow C, Blencowe BJ, Hughes TR (2010) Most "Dark Matter" Transcripts Are Associated With Known Genes. PLoS Biology 8(5):1-21.

186 Comments
Joe Felsenstein · 19 May 2010
Interesting, a good summary.
Opponents of evolutionary biology are always saying that “Intelligent Design predicts that there is no junk DNA”. They also say that ID is not religion but a straightforward scientific theory. Now I can think of theological arguments against the existence of junk DNA (along the lines of “No self-respecting Deity would ...”).
But if we rule out that theological argument, exactly where in ID do this supposed “prediction” come from? I don't recall anything in the writings of Dembski or Behe that makes any such prediction. Does anyone have a non-theology source for it?
Jesse · 19 May 2010
DeityIntelligent Designer would..." This only has any meaning if we know something about the Intelligent Designer. Since, for the ID folks, it is already known a priori that the designer is God and we are made in his image, it all fits in nicely with their little framework.JohnK · 19 May 2010
Dave Wisker · 19 May 2010
How can ID predict that there is no junk DNA? Such a prediction can only be made with theassumption of a design that minimizes genomic waste. But that assumption is based on speculation on the nature of the designer. And that's a non-no, or so the IDers keep telling us.
Henry J · 19 May 2010
Genomic waste? What fraction of a cell's mass is its DNA? If the mass of the DNA is tiny compared to the whole cell, and doesn't require excessive amount of resources to produce and maintain it, then where's the waste?
Dave Wisker · 19 May 2010
Henry J · 19 May 2010
What I'm wondering is how the cost of having the unused DNA compares to the total cost of running the cell. That seems to me to be more important than comparing the cost of the junk DNA to the cost of the functional DNA.
Klaus Hellnick · 19 May 2010
Aagcobb · 19 May 2010
Aha! ID has always predicted that there would be loads of junk DNA, because the human genome has been degrading ever since the Fall, uh, I mean, since the designer designed us! And we've always been at war with Eastasia!
MrG · 19 May 2010
Ichthyic · 19 May 2010
It doesn’t get any better than this!
weren't you banned from here eons ago, John?
do you truly love it so?
aren't you having enough fun arguing with yourself on any of your own blogs?
MrG · 19 May 2010
Nick (Matzke) · 19 May 2010
MrG · 19 May 2010
I once saw a comment someplace that large genomes tend to be correlated with large cells, and that cell size may have selective advantages.
So junk DNA may actually have a function, just as wadded-up pages of newspapers used for packing something fragile in a box have a function. In either case, it's not there to be read.
Ichthyic · 19 May 2010
The genome would be a book that was 75%+ full of gibberish or short repetitive sequence.
heh, I often think most books are.
Ichthyic · 19 May 2010
the end is any time now.
wait, how old are you again, John?
386sx · 19 May 2010
kakapo · 19 May 2010
John Harshman · 19 May 2010
And before that, Masterson, J. 1994. Stomatal Size in Fossil Plants: Evidence for Polyploidy in Majority of Angiosperms. Science 264:421-424.
Abstract: Three published estimates of the frequency of polyploidy in angiosperms (30 to 35 percent, 47 percent, and 70 to 80 percent) were tested by estimating the genome size of extinct woody angiosperms with the use of fossil guard cell size as a proxy for cellular DNA content. The inferred chromosome numbers of these extinct species suggest that seven to nine is the primitive haploid chromosome number of angiosperms and that most angiosperms (approximately 70 percent) have polyploidy in their history.
Stanton · 19 May 2010
Henry J · 19 May 2010
I wonder if the nonfunctional DNA increases the amount of space per useful gene, which might reduce the amount of delays due to DNA readers getting in each others way?
Henry
Intelligent Designer · 20 May 2010
Dale Husband · 20 May 2010
sparc · 20 May 2010
OgreMkV · 20 May 2010
Dave Wisker · 20 May 2010
Pete Dunkelberg · 20 May 2010
Natman · 20 May 2010
ritebrother · 20 May 2010
harold · 20 May 2010
Henry J · 20 May 2010
I don't know why anti-evolutionists worry about whether junk DNA is useful or not in the first place; neither presence nor absence of junk DNA is logically implied by the hypothesis that life was in some way engineered.
Answering that sort of question requires a lot of detail on the methods, motives, and limitations of the engineer(s) that did it, so a wrong answer on this question would mean only that they had the details wrong; it wouldn't impact their central concept.
Dale Husband · 20 May 2010
Intelligent Designer · 20 May 2010
Some might be interested to know that Wikipedia no longer has a entry for Junk DNA. That link now transfers automatically to an entry on Non-coding DNA. Calling it junk in the first place was a blunder.
Natman · 20 May 2010
Dale Husband · 20 May 2010
Intelligent Designer · 20 May 2010
Intelligent Designer · 20 May 2010
eric · 20 May 2010
PZ Myers · 20 May 2010
Wikipedia is grossly wrong. Non-coding DNA and junk DNA are [b]not[/b] synonymous terms, and never have been. Regulatory sequences, for instance, are non-coding, but have never been characterized as junk DNA.
Henry J · 20 May 2010
The Wikipedia article says that much of the non-coding DNA is junk; it doesn't say all of it. It has a section discussing the origin and usage of the term "junk DNA".
Intelligent Designer · 20 May 2010
harold · 20 May 2010
harold · 20 May 2010
harold · 20 May 2010
Dale Husband · 20 May 2010
Natman · 20 May 2010
Henry J · 20 May 2010
Is it that big an error for "junk DNA" to be relegated to a chapter in the article on "non-coding DNA"?
harold · 20 May 2010
Natman -
Actually, I don't at all agree that Wikipedia is wrong here, and I find it to be a very good source for terse, articulate, generally accurate summaries of scientific topics (among other things). A good article will have appropriate references to the original literature, which will themselves have reference sections, so anyone can go deeper with ease.
PZ misunderstood, and thought that Wikipedia had confounded non-coding regulatory elements with the different type of non-coding DNA sometimes referred to as "junk" DNA, which would indeed have been a gross error. That has been cleared up. Wikipedia did not contain this error.
harold · 20 May 2010
Dale Husband -
Whether or not something is called "junk" is a subjective decision. I could call the genes for the most basic and critical metabolic functions "junk" if I felt like it.
There are eukaryotic genes which have arisen from non-coding sequences and mice without certain non-coding sequences are viable but not exactly the same as the mice with the sequences. Whether any of this counts as "function" or not, perhaps another subjective decision, I don't know.
However, if we dogmatically, and against the evidence, suggest that all non-coding DNA is 100% irrelevant, not to say you're doing that but if we do, we risk giving creationists a freebie, allowing them to be "right for the wrong reason".
Intelligent Designer · 20 May 2010
Intelligent Designer · 20 May 2010
harold · 20 May 2010
Intelligent Designer -
First of all, you need a different name, unless you really are a creo, because the one you have now is guaranteed to rub people the wrong way.
I find both of your thoughts interesting. I also think they are both likely to be wrong.
A given absolute quantity of ionizing radiation would provide the energy to theoretically drive up to a given number of mutations. For that reason alone the presence of less relevant base pairs could stochastically shield gene sequences. Your assessment would be correct only if the energy amount of ionizing radiation exposure were always in excess of that required to mutate every base pair in the genome.
As an analogy, imagine if I have a deck of playing cards, and a monster is going to rip up some of the cards. I want a mechanism to make sure he rips up as few real cards as possible. If I add hundreds of blank cards to the deck, and he is equally likely to rip them up, it (imperfectly) protects the real cards. The only way it doesn't is if the monster always can and always will rip up all the cards, no matter how many blanks I add.
I am not endorsing the "protection" hypothesis, I am trying to explain it.
Furthermore, the genome is not physically structured as a one dimensional string of nucleotides. "Junk" DNA could be positioned in a way to be more exposed.
Also, the virus genomes in non-coding DNA are generally so degraded that they no longer code for viable viruses. In fact, if that weren't the case, the viruses they code for would be expressed in our bodies. Viral-induced pathology nearly always requires intact, viable virus reproduction. It is massively, overwhelmingly more likely that these are exactly what they look like - "fossil" remnants of viral infections that our distant past ancestors once had.
Steve P. · 20 May 2010
Intelligent Designer · 20 May 2010
raven · 20 May 2010
raven · 20 May 2010
raven · 20 May 2010
Lion IRC · 20 May 2010
"...we haven't found a function for any of them yet..."
Those few words pack a very big punch -even if you arent an optimist, wishful thinker, open-minded skeptic....
Lion (IRC)
Steve P. · 20 May 2010
Curiously, PZ has bothered to mention Richard Sternberg's response to Ayala and Falk on this subject.
PZ, you're not by any chance peeved that you were not invited to the discussions amonth warring theists?
On second thought, a dangerous notion.
But just in case, PZ. Would you mind giving your take on how and where Sternberg is wrong on the apparent functionality of 'junk' DNA?
In case you may have 'lost' the links, here are the three posts Richard wrote on the subject in March of this year:
http://www.evolutionnews.org/2010/03/ayala_and_falk_miss_the_signs.html
http://www.evolutionnews.org/2010/03/signs_in_the_genome_part_2.html
http://www.evolutionnews.org/2010/03/beginning_to_decipher_the_sine.html
Looking forward to that crushing post where you score yet another triumph, embarrassing the theists for the nth time.
Steve P. · 20 May 2010
Sorry, that should read 'PZ
hashasn't bothered....'John Harshman · 20 May 2010
There seems to be some confusion about the definitions of "junk DNA" and "non-coding DNA", and it's persisted even after PZ's response. Please, people.
Junk DNA is DNA in which particular sequences have no function (though I would allow bulk functions, like the possible selection for cell size mentioned above). We can distinguish junk DNA not because it has no known function but because it evolves at the mutation rate, i.e. neutrally.
Non-coding DNA is just that: DNA that isn't translated into protein using the genetic code. A fair amount of non-coding DNA has a function: functional RNAs, regulatory sequences, and a few other conserved regions whose functions are unknown (but we know they have functions because they evolve more slowly than the mutation rate).
All junk DNA is non-coding, but not all non-coding DNA is junk, and it would be foolish to dispose of either term, since they have useful and separate meanings.
Pinko Punko · 21 May 2010
The paper looks at poly-A+ RNA, so this isn't really the book on transcription.
Scott · 21 May 2010
I recall learning recently about how DNA transcription really works. In all the idealized renderings I'd seen previously, the DNA is unzipped into long straight rails that the RNA enzymes work on. But (IIRC) the DNA double helix is normally wound and folded rather tightly (and precisely), as though on a spool, and the double helix is only "loosened" enough for the transcription process. More importantly, it's typically not the actual sequence itself (of either DNA, RNA, or the resulting protein) that is important, but rather it is the 3 dimensional and electrical structure of the molecules that make them useful. Also, with the multiple windings of DNA, the interesting interactions can sometimes be between pieces of DNA that are not right "next to" each other in terms of base-pair separation, but which might end up "next to" each other physically when wound and folded in their normal manner. I wonder (as harold suggested earlier) whether the "junk" DNA might serve some sort of "structural" or "buffer" function, keeping other "functional" pieces at just the right separation for proper transcription or methylation . The actual content of (or kinds of base pairs in) the "buffer" might be immaterial, and so does not need to be conserved. Perhaps what might be important is the number of base pairs in the "buffer" region? Has there been any research along those lines?
Of course, I could be remembering this incorrectly, and ending up way off base here. I'm no biologist. Just a curious amateur.
On a slightly different topic, while there is a lot of DNA that doesn't code for anything in a mature cell, have we learned enough about evo-devo yet to say whether some of this "junk" DNA doesn't have some function in the early development cycles of the embryo? (Though, finding that much of the "junk" DNA is not conserved, probably argues against that idea anyway.)
harold · 21 May 2010
John Harshman · 21 May 2010
DS · 21 May 2010
harold wrote:
"ID/creationists are forced by their ideology to deny the evidence and insist on “function” for all of non-coding DNA.
The rest of us can go with the evidence, but the evidence doesn’t necessarily suggest that junk DNA has no impact whatsoever."
Right. But the thing is that the rest of us are not forced to assume that all the DNA was poorly designed either. The fact that DNA can evolve cannot be used as evidence that it cannot evolve.
raven · 21 May 2010
harold · 21 May 2010
John Harshman -
"However" because once a segment of DNA gets the regulatory elements to be a gene, and can at least potentially be a template for expression of RNA and/or protein (depending on regulation), then that sequence might (or might not) become subject to selective pressure related to whatever impact the RNA or protein might have on the cell.
In contrast to a completely non-regulatory, non-coding sequence, which would probably be under very little to no selective pressure directly related to the nucleotide sequence.
(It's also true that junk DNA overall does not have entirely random sequence. It's full of repetitive elements. For whatever reason, those repetitive elements were "selected" to be spread around the genome, relative to other sequences. I have no idea why this is - it could be that these particular sequences are simply more likely to provoke duplication mutations when they are being replicated.)
Obviously, we are in complete agreement on this subject. So-called junk DNA does not code for genes, by definition. The sequence of junk DNA in general is not subject to the selective pressure the way the sequences of many genes are, which is strong evidence that the exact nucleotide sequence of junk DNA is not germane to any major cellular function.
However, some or all of this DNA may have impact on the cells that contain it. It is a poorly understood area. The mouse evidence both demonstrates that the (studied) areas of junk DNA do not contain any elements which are critical to basically normal mouse development and physiology. Yet it also illustrates a possible subtle but relevant metabolic impact of having or lacking the sequences that were studied. The fact that genes can arise from such DNA is another potential type of impact.
The arguments of ID/creationists on this subject reflect deep ignorance, commitment to a rigid, irrational ideology, and the lack of ethical character which permits them to deliberately "fake" scientific authority while actually hurling out verbose nonsense.
Indeed, the very existence of junk DNA reveals their hypocrisy. They claim that they merely seek evidence for some non-specific "designer". Yet they implicitly seek to imbue this "designer" with the traits of their post-modern, politically motivated god. The only reason junk DNA is a challenge to them is because a "benign", human-like designer (even by their twisted idea of what is "benign") would not be expected to create it.
harold · 21 May 2010
Raven -
Yes, we are in total agreement, and it is clear that much of the repetitive sequence type of junk DNA, for example, can vary greatly between individuals with literally no apparent impact whatsoever.
It is an interesting topic, among many, for rational people, and one of many insurmountable problems for creationists.
hoary puccoon · 21 May 2010
Scott said: "...it’s typically not the actual sequence itself (of either DNA, RNA, or the resulting protein) that is important, but rather it is the 3 dimensional and electrical structure of the molecules that make them useful."
Can someone tell me if that's correct? I was under the impression that the sequence of DNA and consequently messenger RNA was extremely important, and that the "3 dimensional and electrical structure of the molecules" was most salient with proteins.
harold · 21 May 2010
hoary puccoon -
It is absolutely the sequence of nucleotides in a gene that codes, through the intermediate of mRNA, for the amino acid sequence of the protein. Downstream processing may impact on whether and where the protein is truncated, glycosylated, etc. The amino acid sequence of the protein, in conjunction with chemical modifications like glycosylation, if present, will determine its three dimensional structure. Proteins "fold" spontaneously into their three dimensional structure.
Regulatory elements work largely through nucleotide sequence as well.
Chemical modifications of individual nucleotides, such as methylation, can be important as well.
“3 dimensional and electrical structure of the molecules” has a lot to do with how eukaryotic chromosomes are packaged into the nucleus, though. http://en.wikipedia.org/wiki/Chromosome
hoary puccoon · 21 May 2010
harold--
Thanks. You confirmed what I had understood.
Pinko Punko · 21 May 2010
hoary,
Scott is referring to the fact that genomes are packaged three dimensionally in space, and in certain instances a specific conformation is important for a process. For example, bringing a very distant regulatory region (of specific sequence) close to another region (of specific sequence). Here both the sequence of the DNA and the arrangement of the chromosomal ultrastructure are important.
hoary puccoon · 22 May 2010
Pinko Punko--
Thanks to you also. Knowing more about the history of science than about science, it's amazing to me what is now known.
Andrew Stallard · 22 May 2010
Henry J · 22 May 2010
Rolf Aalberg · 23 May 2010
GODISNOWHERE · 23 May 2010
Let's call a spade a spade. A good old boys club is just that. Peer review shmeer review. If I can get an alliance of like minded people to write articles agreeing with my premise that junk DNA lead to vertical and not horizontal stripes on zebras, then, according to the good old boys club rules, I must be right! You can call certain strands of DNA junk, but these strands exist, and I'll assert that the label has an agenda behind it. If DNA, that is not "junk" is the "worthy" DNA, then let's apply this to all the scientists perpetuating peer reviewed articles, these would be the "worthy scientists". Are the remainder of scientists merely, "junk scientists"? I browsed your Expelled category and the length to which you defend your theory of evolution is no surprise. It is, after all your religion. What I could not ignore is the reality, and I need no peer review for this observation, that the ID scientific community embarrassed the "...life came to earth on the back's of crystals..." evolutionary scientific world view community.
Stanton · 23 May 2010
MrG · 23 May 2010
Stanton · 23 May 2010
Stanton · 23 May 2010
MrG · 23 May 2010
Malchus · 24 May 2010
Intelligent Designer · 24 May 2010
fnxtr · 24 May 2010
(shrug) Okay. All you have to do is show what all these repetitive or non-coding or apparently non-functional regions actually do, and why they're not really just broken genes, dead retroviri, and so on, even though that's what they appear to be to anyone who knows what they're talking about.
Until then, I'm going to side with the men and women who make it their livelihood to work with and understand this stuff, rather than armchair quarterbacks and Aristotlean mind-wankers.
(See, I knew we'd get to the "DNA is like computer code" sooner or later. To a man with an ax, everything looks like a tree.)
Intelligent Designer · 24 May 2010
Well, repetition isn't unique to software binaries. It is found in all kinds of information. Open your computer and look at the circut boards. What you will find are the same jobbers being used over and over again. Same thing with the English language or any written language. Repetition is a hallmark of information, not the other way around.
MrG · 24 May 2010
hoary puccoon · 24 May 2010
Intelligent Designer--
We all get why a cdesign proponentsist like yourself would be so enamored of repetition-- it's all the scientific creationist crowd does.
But could you put aside for one moment how much the Christian dominionists are paying you, and look at this from the point of view of the poor scientist in the lab? How does the fact that there are useful repetitive elements in a computer program translate into publishable scientific research in biology? Scientists are arguing for Junk DNA because they can't find any way in which that DNA is coded into anything useful. If they do find it's useful in some way, they will be eager to publish those results, and the peer-reviewed journals will be eager to accept them.
Blathering about an analogy to computer code adds nothing to the research one way or the other. I could argue that evolution is true because the electrical system in my 20-year-old sailboat looks like it evolved, instead of being designed (worse luck!) But that would be no help to, say, a paleontologist trying to tease out the relationships between hominid fossils.
What you wrote did nothing except make ID look like a vacuous word game. If that was your intent, of course, please proceed.
Curious · 24 May 2010
Paul Zachary, please give us your understanding of the term "junk DNA" so that it does not become some superfluous idea without meaning. Can you please provide a test or experiment to verify whether a sequence is in actual fact "junk DNA".
I am looking forward to your answer so that I can commence in the lab to actually try and find this so-called "junk DNA".
eric · 24 May 2010
fnxtr · 24 May 2010
Check and mate. Well played, eric.
Malchus · 24 May 2010
Intelligent Designer · 24 May 2010
Malchus · 24 May 2010
Randy, I would draw your attention to Pharyngula, where Myers has just written an entire post demolishing your claims. He writes well, though I disagree with his theological position; you will find that he and commenters have exhaustively dealt with your errors and misconceptions.
Intelligent Designer · 24 May 2010
RBH · 24 May 2010
Malchus · 24 May 2010
Intelligent Designer · 24 May 2010
aiguy · 24 May 2010
Is anyone aware of the fact that Dr. William Dembski, in his book "The Design Revolution", makes it quite clear that ID is completely consistent with the expectation that junk DNA will clutter the genome?
Read the following (emphasis added). After explaining how intelligent designers (human computer programmers) were apt to leave dead code in their programs, Dr. Dembski explains:
However, the dead code can happily sit in the source code (as perhaps can the 'junk' DNA stay in the DNA) forever - doing nothing but causing confusion to later intelligent observers - engineers who must update the program for example.
http://www.iscid.org/encyclopedia/Optimal_Design,_Argument_From
DS · 24 May 2010
Malchus · 24 May 2010
aiguy · 24 May 2010
DS (and Malchus), you misunderstood completely.
The point is that while IDers claim that ID predicts that junk DNA will be found to be functional, it turns out that their leading light Dr. Dembski himself had already admitted that Junk DNA (or its absence) is perfectly consistent with ID! His book "The Design Revolution" was published in 2004, before IDers started blabbing about these junk DNA "predictions". I guess they just didn't notice that Dembski had already claimed that junk DNA was no problem for ID. So for IDers to now suggest that their theory "predicted" that junk DNA was actually functional is even dumber, considering that Dembski had already discounted any such prediction.
Get it?
DS · 24 May 2010
derwood · 24 May 2010
Intelligent Designer · 24 May 2010
Malchus · 24 May 2010
Ian Musgrave · 24 May 2010
Ichthyic · 24 May 2010
Stimpy sez:
PZ did not site [sic] any facts in his post that I am not aware of.
more's the pity then, since we said the same things to you years ago, and you're still making the same basic errors in fact and logic.
I feel sorry for you, I truly do, that since apparently this is such an important issue to you, you would fail to even bother to try and learn the basic biology that would inform you enough to make cogent statements.
that you see no problem with stumbling blindly forward in your attempts to outdo Don Quixote suggests to me you have mental issues to deal with.
deal with that first, then take some classes in basic biology and genetics, THEN come back if you manage to produce a model, or an argument, that makes sense.
Malchus · 24 May 2010
Henry J · 24 May 2010
Jess Tauber · 24 May 2010
There is an already large and growing set of parallels of structure and function between genome/proteome and human language- much more than any of you have been led to believe.
Sequences outside of protein-coding sequences (and some inside) act like grammar and pragmatic coding elements in languages. Some of the latter are based on repetition and rhythm patterns, others on stress/prosody, order of elements (as we also see in the genome). Others (morphology, closed-class forms) derive from the lexicon, utilize segments instead of prosody, etc., and end up competing with the latter for influence.
But the prosodic/rhythmic/order parts of the system are also capable of generating new sequences with segments (consonants, vowels, etc.)- and when they do so, these have an iconic relationship with their meanings (sound symbolism), that utilizes the internal geometry and symmetry of the phonological system itself to pattern the meanings (diagrammatical iconicity).
What goes on in the genome/proteome is largely parallel- in organization, in function, and in evolution. Each morphosyntactic type of language associates with a type of genome. Lots more. This isn't the place to expand on all this though.
However, this kind of parallelism with function, loss of function and refunctionalization, cycles, types, shift from iconicity to symbolicity to indexicality and back again can arise without any need for an outside intelligence pushing things along. There is even evidence that the periodic table has been part of a similar evolution, given that the properties of elements (even basic electronic configurations) can't be read right off the chart. Outer context is involved too.
Jess Tauber
Dale Husband · 24 May 2010
Rolf Aalberg · 25 May 2010
Curious · 25 May 2010
PZ Myers · 25 May 2010
Nobody in the world calls me "Paul Zachary" or "Zachary". It's pretty much a dead giveaway that you're being some kind of pompous smartass. So I'm sorry, I don't believe your question is at all sincere, and you can go jump in a lake.
After you've dried out, though, you could pay attention to the scientific literature and the other people here, and look into comparative and functional studies. Junk is the stuff that doesn't do anything if you remove it and that shows relatively little conservation.
And that's more of an answer than a pretentious ass deserves.
eric · 25 May 2010
Curious · 25 May 2010
John Harshman · 25 May 2010
Hey, I think Mr. Curious has an interesting point. Junk DNA is as junk DNA does. HeLa has a bit more junk than the human genome does, though it hasn't had much time to show the diagnostic markings (i.e. neutral evolution, lack of expression, etc.). We all know the primate GULO gene is junk DNA; HeLa just contains a great number of genes that are useless, most of them never expressed, in its environment.
I'm not sure what his point was intended to be -- probably something stupid but snarky -- but that's a nice thought.
Ian Musgrave · 25 May 2010
John Harshman · 25 May 2010
Joe Felsenstein · 25 May 2010
John Harshman · 25 May 2010
Curious · 26 May 2010
It seems my initial celebration for finding junk DNA would have been premature. However I would like to hear from Zachary.
So let's ramp up the experiment a little.
HeLa cells have been used in many labs. Now let's say I collect HeLa cells from 10 different laboratories from all over the world. Not all of them will be genetically identical (in fact none of them will be) of course since they will have had different selection pressures and different random variation events (mutations, mitotic slippage etc.).
I do a few experiments:
Cell viability and cell growth tests,
Cell cycle analysis,
Autophagic and apoptotic activity,
Gene expression analysis (microarrays),
Protein expression analysis (protein arrays),
ROS production analysis,
Mitochondrial membrane potential analysis,
A few morphological studies (TEM, SEM, live cell imaging etc.),
Sequencing and karyotyping of the genomes.
After all this work (phew, I can see a PhD for a student from this), I hypothetically find that 3 of the cell lines from the different labs are very similar in all the parameters except for the sequence difference.
In other words, the 3 cell lines mentioned have similar cell viability, cell growth, cell cycle, autophagic, apoptotic, gene and protein expression analysis, ROS production, mitochondrial membrane potential, morphological and karyotype profiles, but they vary considerably in certain regions of the genome, say for example on chromosome 4.
I discover that these regions are non-coding and removal of these sequences has no effect on the abovementioned parameters.
Am I to celebrate all of a sudden (now) and claim I have found myself some junk DNA?
Malchus · 26 May 2010
Curious · 26 May 2010
Malchus, would you claim you have found junk DNA from the above example?
Btw, the author's name is Paul Zachary Myers, and I am still awaiting a reply from him. If he does not want to reply, it is understandable. Calling a person by their name can be a traumatic experience I guess. My apologies.
Malchus · 26 May 2010
Malchus · 26 May 2010
By the way, if you are unable to understand that you have already been answered, I would suggest you look to the prior posts on this and the preceding page.
Malchus · 26 May 2010
Curious · 26 May 2010
Dave Luckett · 26 May 2010
Professor Myers is a full professor of an esteemed University, you are asking him to respond in his professional capacity, and you plainly do not know him personally. It is grossly rude of you to call him by his middle name. He's "Professor Myers" to you.
The response of a gentleman to gross rudeness is to ignore the person offering it.
Curious · 26 May 2010
Curious · 26 May 2010
Dave Luckett · 26 May 2010
In other words, you demand of him behaviour that you do not display yourself. Thus, you have passed from "boor" to "hypocrite" in one easy thrust of the spade. But by all means, keep on digging.
Curious · 26 May 2010
Dave Luckett.
I do not pretend to be behaving like a Professor and a gentleman, you are of course suggesting he is a gentleman and he is afterall a Professor. If he is a gentleman, then I suggest he behaves like one and ignore the non-gentleman-like behaviour of others and stick to the topic at hand.
Dave, now could you be like a gentleman and also at least try and give an answer to the question. I fear these squabbles you are trying to fuel are not going to lead to anything meaningful.
I'll ask you again:
In this example (http://pandasthumb.org/archives/2010/05/junk-dna-is-sti.html#comment-218018), can I claim to have found junk DNA? If not, how ould you improve the experiment to verify the presence of junk DNA?
Thanks.
Dave Luckett · 26 May 2010
As I remarked, he is displaying the behaviour of a gentleman by ignoring you. As do I, henceforth.
Dave Lovell · 26 May 2010
Dave Wisker · 26 May 2010
Stanton · 26 May 2010
phantomreader42 · 26 May 2010
Curious · 26 May 2010
It seems to experimentally verify junk DNA is a meaningless task and not worth pursuing since the concept itself is scientifically vacuous. Sort of like ID.
fnxtr · 26 May 2010
No-one's got a gun to your head, Curious. You are free not to pursue this line of inquiry any farther, since you clearly think it unimportant.
See ya.
Malchus · 26 May 2010
eric · 26 May 2010
curious · 27 May 2010
Junk DNA as a colloquialism seems to merely apply to DNA that is a provisionally labeled for sequences of DNA for which no function has been identified.
And of course, I will leave it to you to try and figure out a proper definition of "function" as it applies to the colloquialism... junk DNA.
It however does not imply that junk DNA is functionless since that would merely be an argument from ignorence...like ID. Besides, I don't think a single person will argue that sequences of DNA for which no function has been identified will never even have the potential to be functional given random variation and selection. That is just another argument from ignorance...like ID.
Jesse · 27 May 2010
Curious · 27 May 2010
eric · 27 May 2010
Stanton · 27 May 2010
John Harshman · 27 May 2010
harold · 27 May 2010
Curious -
You are certainly wasting a great deal of time on stupid semantic games.
It is common to refer to non-coding DNA that does not show the type of sequence preservation we would expect, if sequence changes were selected against, as "junk DNA".
This usage is conventional rather than technical. You don't have to call anything "junk" DNA if you don't want to.
You appear to worship a god who encourages obnoxious, confrontational behavior, or at least, adhere to an ethical system that does so. You appear to feel that your god or ethical system is somehow threatened if some segments of DNA in eukaryotic cells have little or no "function". That is entirely your own self-created personal problem.
In many cases, deletions of large amounts of this DNA from cells appears to have no obvious strong impact on the phenotype.
I and others among those who respect and basically agree with PZ Meyers have pointed out, repeatedly, that subtle impacts of deleting such DNA have also been observed, in some cases. The origins and impact of the diverse varieties of non-coding DNA remain, to some of us, an interesting area of study.
Unfortunately, at least based on your posts here, you are not qualified to meaningfully contribute to this area of study. Your emotional biases are too severe to allow you to function in a relevant way.
1) You are obsessed with the trivial semantics of the term "junk" DNA rather than interested in actual results and observations.
2) You claim an interest in the area, but are so ignorant of prior research that you don't even know the things that a google search would reveal. Failure to familiarize oneself with the work which has already been done is a non-starter in scientific research.
3) You are unable to discuss the evidence in a civil, collegial way with those who are knowledgeable in the field.
Dave Lovell · 27 May 2010
eric · 27 May 2010
Henry J · 27 May 2010
But does creationism necessarily logically require the absence of detritus?
But then again, theism in general doesn't logically require the absence of evolution, either - the claimed inconsistency there is because of assumptions about the details of a particular version of theism, not the basic concept.
harold · 27 May 2010
Eric -
Yes, ultimately, that is the point.
I do have a minor problem with anthropomorphic, subjective terms like "junk", or even "detritus". I even have a problem with semantic issues revolving around the word "function". I have a problem with making statements that go (even if only slightly) beyond the evidence.
But at the end of the day, non-coding, not-directly-regulatory DNA just isn't a problem for the theory of evolution, no matter what. And it never has been seen as one.
Some people have invented a god or philosophy whose existence or validity is incompatible with the existence of non-coding DNA.
Well, that's just tough for them. There is a lot of non-coding DNA. Their particular god or philosophy must be false (and usually is for many other reasons as well). Their denial often takes the form of ludicrous, uninformed, insultingly ignorant "conjecturing" about "junk" DNA. But the problem is entirely theirs.
eric · 27 May 2010
Mike Elzinga · 27 May 2010
MrG · 27 May 2010
Stanton · 27 May 2010
Stuart Weinstein · 29 May 2010
Stuart Weinstein · 29 May 2010
harold · 30 May 2010
PZ Myers · 30 May 2010
Does. Not. Work.
There is no arbitrary mechanism that says the genome only gets X number of mutations per replication event. The rate is per nucleotide.
If you have an error rate of 10 in 52 for your deck of cards, the original deck will have, on average, 10 errors per year. Your inflated deck of 520 cards will have, on average, 100 errors per year, 10% of which will fall on the original good cards, or 10 errors that matter. Same number.
John Harshman · 30 May 2010
Ben Vallejo · 1 June 2010
Ben Vallejo · 1 June 2010
fnxtr · 1 June 2010
Ben, first of all, quoting Dr. Dr. D and The Pastor Dave of ID are not going to gain you any traction here.
Second, did you even read the original post?
SWT · 1 June 2010
Henry J · 1 June 2010
As I recall, the presence of a lot of junk (i.e., unused) DNA wasn't predicted prior to its discovery, nor is it necessarily entailed by the current theory.
Also, I don't see any reason why "life was deliberately engineered" would necessarily imply the absence of unused DNA, anyway. So if either its presence or absence is consistent with either ToE or "IDC", then why are anti-ToE advocates fussing about this particular detail?
I don't get it.
Henry J
Pauli Ojala · 2 June 2010
Creationists have campaigned for Devolution. That is, decay and disintegration of the biosphere, really, universe itself.
Genome contains bewildering amount of retroviral rubbish, maybe even 1/10 of it. Estimates for the intergenic transcripts are 4-20% of all genes. Spliceisoforms have steadily increased to an estimate of over 80% of the genes. I think these structural degenerations may well end up contributing to disease, pathology and death. Let us remember that even the poisons aka viruses are not poisonous until they lyse the cells. Only now have we begun vaccinating against parvo virus etc. that may be causative agents to poking DM type I even.
http://www.helsinki.fi/~pjojala/Haeckelianlegacy_ABC5.pdf
Henry J · 3 June 2010
MrG · 3 June 2010
fnxtr · 3 June 2010
We lost our tails
Evolving up
From little snails
I say it's all
Just wind in sails...
stevaroni · 3 June 2010
fnxtr · 3 June 2010
There's probably a fetish website for that, too.
Intelligent Designer · 4 June 2010
PZ Myers · 4 June 2010
Inventing a new pseudoscientific term for a phenomenon which has no empirical evidence for its existence except for a brief mention on your dismally malinformative blog is not a rationale, Mr Stimpson.
MrG · 4 June 2010
See the "TV Tropes" website entry on "Applied Phlebotinum" for insight:
http://tvtropes.org/pmwiki/pmwiki.php/Main/AppliedPhlebotinum
eric · 4 June 2010
Intelligent Designer · 4 June 2010
SWT · 4 June 2010
SWT · 4 June 2010
Intelligent Designer · 4 June 2010
SWT · 4 June 2010
Mac McCarthy · 15 August 2010
I'm late to this party, but I've been puzzled at the apparent controversy over so-called Junk DNA.
Imagine a world in which the evolutionary hypothesis is true. As evolution progresses, one would *expect* the process to be messy and leave behind nonfunctional pieces. Nobody would expect the process of evolution to 'clean up' after itself. Would we? Unless there were an evolutionary advantage to doing so, and it seems more likely there would be lots of 'junk' lying around that had a purpose when it started and no long does.
A billion years of evolution, a billion years of evolutionary trash left behind - not only is that not surprising, it would be mighty surprising if it were any other way. It seems to me inevitable that some features of the genome will be nonfunctional left-behinds. So what's the big deal?
Henry J · 15 August 2010
That's exactly right - as I understand it, there is no big deal scientifically, and you're probably right that there would be if there wasn't a lot of junk. (Although I do recall that the prevalence of junk wasn't predicted ahead of time.)