Correct me if I am wrong, but was it not Darwinists who long maintained that 'JUNK DNA' served no purpose, where skeptics long suspected it did?
You are wrong.
By 'skeptics', I think you mean creationists and Intelligent Design advocates.
Yes, they like to claim that they 'believed' all along that was no junk DNA - but not because of anything scientific. And they just claimed victory after-the-fact, without bothering to look at the scientific literature.
According to John West of the Discovery Institute, the first "prediction" that junk DNA would be functional was made in print by Bill Dembski in an essay from 1998, and had been implied in a rejected letter to the editor in
Science penned by creationist electrician Forrest Mims in 1993.
Problem was, actual scientists had been speculating, predicting, and finding some function in some noncoding DNA a decade or more prior to the anti-evolution "skeptics" writing their little essays - just 2 examples:
Cell. 1975
Feb;4(2):107-11.
The general affinity of lac repressor for E. coli DNA: implications for gene regulation in procaryotes and eucaryotes.
By equilibrium competition experiments, the dissociation constant (K(RD)) of lac repressor for E. coli DNA carrying a deletion of the lac operon was measured at a variety of salt concentrations. These data are used in the consideration of several aspects of protein-DNA
interaction: Quantitative estimates of specificity are made. Specificity changes only slightly with salt concentration. We calculate that in vivo, 98 percent or more of repressor is bound to DNA predominately at sites other than the lac operator. Inducers shift repressor from operator to nonoperator DNA, but do not free it from DNA. The general affinity of repressor
for E. coli DNA is sufficient to support a model where repressor slides along DNA for significant distances. The effective dissociation constant of repressor for operator (K(eff)) is very sensitive to the total DNA concentration. We propose that "junk" DNA in eucaryotes functions to maintain total DNA at an optimum concentration. We consider the lac operon in the nucleus of a lymphocyte, point out that severe difficulties would be encountered, and suggest possible solutions.
Or Zuckerkandl from 1981:
A general function of noncoding polynucleotide sequences
Abstract
It is proposed that a general function of noncoding DNA and RNA sequences in higher organisms (intergenic and intervening sequences) is to provide multiple binding sites over long stretches of polynucleotide for certain types of regulatory proteins. Through the building up or abolishing of high-order structures, these proteins either sequester sites for the control of, e.g., transcription or make the sites available to local molecular signals. If this is to take place, the existence of a c-value paradox becomes a requirement. Multiple binding sites for a given protein may recur in the form of a sequence motif that is variable within certain limits. Noncoding sequences of the chicken ovalbumin gene furnish an appropriate example of a sequence motif, GAAAATT. Its improbably high frequency and significant periodicity are
both absent from the coding sequences of the same gene and from the noncoding sequences of a differently controlled gene in the same organism, the preproinsulin gene. This distribution of a sequence motif is in keeping with the concepts outlined. Low specificity of sequences that bind protein is likely to be compatible with highly specific conformational changes.
One can find an extensive list of citations and commentary on junk DNA here:
junk DNA « Genomicron
Of special interest are those tagged ENCODE:
ENCODE « Genomicron
A nice
summary of 'junk' in the genome from biochemist Larry Moran:
Junk in Your Genome
Transposable Elements: (44% junk)
DNA transposons:
active (functional): <0.1%
defective (nonfunctional): 3%
retrotransposons:
active (functional): <0.1%
defective transposons
(full-length, nonfunctional): 8%
L1 LINES (fragments, nonfunctional): 16%
other LINES: 4%
SINES (small pseudogene fragments): 13%
co-opted transposons/fragments: <0.1% a
aCo-opted transposons and transposon fragments are those that have secondarily acquired a new function.Viruses (9% junk)
DNA viruses
active (functional): <0.1%
defective DNA viruses: ~1%
RNA viruses
active (functional): <0.1%
defective (nonfunctional): 8%
co-opted RNA viruses: <0.1% b
bCo-opted RNA viruses are defective integrated virus genomes that have secondarily acquired a new function.Pseudogenes (1.2% junk)
(from protein-encoding genes): 1.2% junk
co-opted pseudogenes: <0.1% c
cCo-opted pseudogenes are formerly defective pseudogenes those that have secondarily acquired a new function.Ribosomal RNA genes:
essential 0.22%
junk 0.19%
Other RNA encoding genes
tRNA genes: <0.1% (essential)
known small RNA genes: <0.1% (essential)
putative regulatory RNAs: ~2% (essential) Protein-encoding genes: (9.6% junk)
transcribed region:
essential 1.8%
intron junk (not included above) 9.6% d
dIntrons sequences account for about 30% of the genome. Most of these sequences qualify as junk but they are littered with defective transposable elements that are already included in the calculation of junk DNA.Regulatory sequences:
essential 0.6%
Origins of DNA replication
<0.1% (essential) Scaffold attachment regions (SARS)
<0.1% (essential) Highly Repetitive DNA (1% junk)
α-satellite DNA (centromeres)
essential 2.0%
non-essential 1.0%%
telomeres
essential (less than 1000 kb, insignificant)
Intergenic DNA (not included above)
conserved 2% (essential)
non-conserved 26.3% (unknown but probably junk)
Total Essential/Functional (so far) = 8.7%
Total Junk (so far) = 65%
Unknown (probably mostly junk) = 26.3%
And from the same source, a nice review of Jon Wells - the fellow that took more than 10 years to earn his PhD, and had a whole 2 publications as a result - book on junk DNA. Part 1 (of several):
Sandwalk: The Myth of Junk DNA by Jonathan Wells