Date: Thu May 01 2003 - 12:42:34 EDT
Of course some small or large portion of "pseudogenes" and various other
repetitive DNA (e.g, intergenic spacers) will be found in time to have some
function at some level (if only to stabilize surrounding gene expression or
something equally subtle). For this reason, the common term "junk DNA" is
not as appropriate as its common use has indicated. Nevertheless, however
many cases of function that are discovered for particular "pseudogenes",
there will many others for which no function will ever be found. Indeed,
one can demonstrate this in lab organisms by deleting the supposed "junk"
and showing that it makes no difference to the organism. Probably this has
been done. Certainly, there are many examples that show the relative
release from selection (greater mutation rates, especially at positions
that correspond to different amino acids in the parent gene) in
pseudogenes, and this indicates a relative release from function
I've been out of the evolutionary biology research sphere for a couple of
years now (my Ph.D. research was on concerted evolution of ribosomal DNA
intergenic spacers). However, as I remember, even when we used to throw
around terms like junk DNA and pseudogenes, we always understood that some
function will be attributable to particular examples as more research is
done. My overall point here is that I think you are incorrect in implying
that this information you cite somehow overthrows evidence for evolution in
any way. In my opinion, the abstract below is strong evidence for
evolution, not against. It shows how functional complexity can arise by
such gene/pseudogene duplication and redundancy. It is evidence for a
gifted creation (RFEP) that the new layers of subtle functions arise by
mutation of existing genetic material rather than by de novo genes inserted
manually by an intellegent designer.
<jbembe@hotmail. To: email@example.com
Sent by: Subject: Pseudogenes: Molecular Fossils or Functional Elements?
Uh oh! Pseudogenes with a function! This discovery casts another doubt on
our list of solid evolutionary "proofs." See the following commentary on a
Maybe genomes aren't simply littered wastelands of evolutionary byproducts,
but are composed largely of important elements that contribute to the
purposeful generation of organisms? Ridiculous idea, to be sure. I have
always found arguments concerning the sloppiness of design in biology to be
extremely inept for supporting evolution. If you have billions of years of
evolutionary processes to work on refining something through random
and natural selection, waste should be eliminated not accrued. At the same
time, it remains an open question as to how much function and purpose all
elements of the genome have in terms of biological activity. But of
for the adamant evolutionist, even if pseudogenes aren't molecular fossils,
the function they retain simply shows us the creativity of evolutionary
processes, right? Thus can any evidence negate/ bring question to the
veracity of evolution? This article characterizes the whole scenario as a
product of evolution despite the fact that the finding challenges the
long-held belief that pseudogenes are waste products of evolution. Now
aren't necessarily waste, but we *know* that they are still byproducts of
evolution. Provocative finding indeed!!
Molecular biology: Complicity of gene and pseudogene
JEANNIE T. LEE
Jeannie T. Lee is at the Howard Hughes Medical Institute, Department of
Molecular Biology, Massachusetts General Hospital, and the Department of
Genetics, Harvard Medical School, Boston, Massachusetts 02114, USA.
'Pseudogenes' are produced from functional genes during evolution, and are
thought to be simply molecular fossils. The unexpected discovery of a
biological function for one pseudogene challenges that popular belief.
Pseudogenes are defective copies of functional genes that have accumulated
to an impressive number during mammalian evolution1. Dysfunctional in the
sense that they cannot be used as a template for producing a protein,
pseudogenes are in fact nearly as abundant as functional genes2, 3. Why
mammals allowed their accumulation on so large a scale? One proposed answer
is that, although pseudogenes are often cast as evolutionary relics and a
nuisance to genomic analysis, the processes by which they arise are needed
to create whole gene families4, such as those involved in immunity and
smell. But are pseudogenes themselves merely by-products of this process?
do the apparent evolutionary pressures to retain them hint at some hidden
biological function? For one particular pseudogene, the latter seems to be
true: elsewhere in this issue (page 91), Hirotsune and colleagues5 report
the unprecedented finding that the Makorin 1-p1 pseudogene performs a
specific biological task.
Hirotsune et al.5 had been analysing mice in which copies of a fruitfly
called Sex-lethal were randomly inserted in the mouse genome. In the course
of their studies, they encountered one mouse line that died shortly after
birth from multi-organ failure. As this occurred in only one mouse line out
of many, the results could not be explained by aberrant Sex-lethal
expression. Instead, the authors attributed their finding to a disruption
the particular stretch of genomic information into which Sex-lethal had
inserted in this case. Whereas some might have dismissed the line as an
aberration and unworthy of the effort required to characterize it,
and colleagues delved deeper and were rewarded with the surprising finding
that a pseudogene can regulate the expression of the functional gene from
which it arose.
The authors first found that, in the mouse line in question, the inserted
Sex-lethal gene disrupted Makorin1-p1 ? a pseudogene copy of the functional
Makorin1 gene. Only recently identified6, Makorin1 is an ancient gene that
has been evolutionarily conserved from nematode worms to fruitflies and
mammals, and encodes a putative RNA-binding protein. It is the prototype of
a large family of Makorin genes and pseudogenes, and is located on mouse
By contrast, Hirotsune et al. found that the pseudogene Makorin1-p1 lies on
chromosome 5. Like the original gene, this pseudogene can be 'transcribed'
into a messenger RNA copy. But it has incurred mutations during evolution,
so the mRNA cannot, as is usual, be used to produce a protein. Further
differences between the gene and pseudogene include the fact that the
Makorin1-p1 mRNA contains only the first (that is, 5') 700 nucleotides of
the Makorin1 mRNA. Moreover, whereas both copies (one from the mother and
one from the father) of the Makorin1 gene can be transcribed, the
Makorin1-p1 pseudogene is paternally 'imprinted', so that only the paternal
copy is expressed.
Normally, Makorin1 mRNA is expressed throughout the animal6. But Hirotsune
et al. found that when the paternal Makorin1-p1 pseudogene was disrupted,
the expression of Makorin1 was markedly reduced in embryos and throughout
birth and weaning. This implies that the pseudogene is normally required
the high-level expression of Makorin1. Interestingly, of the two forms of
Makorin1 mRNA, only the smaller 1.7-kilobase transcript was downregulated ?
the larger 2.9-kilobase copy was unaffected. The long and short forms are
identical except in a region at the so-called 3' end that is not translated
into protein. So, it seems that this region in the long form functions
independently to keep expression levels high.
The authors also wondered whether the imprinting of Makorin1-p1 is
mechanistically central to Makorin1 expression. However, its disruption had
equal effects on both maternal and paternal Makorin1 genes. So it seems
the imprinting of Makorin1-p1 is an odd happenstance that has little or
nothing to do with its function. Rather, it seems likely that, when
Makorin1-p1 arose, it fortuitously integrated into a chromosomal region
was already imprinted.
This study5 generates many new and exciting questions. For instance, is
Makorin1-p1 the only Makorin pseudogene that regulates Makorin1?
that disruption of Makorin1-p1 causes only a partial loss of expression of
the functional gene, one might speculate that there are indeed other
pseudogenes whose functions partly overlap, and that the deployment of an
entire pseudogene battalion might be a feasible strategy of gene
Furthermore, how does Makorin1-p1 regulate Makorin1? The authors found that
the 700-nucleotide 5' region of Makorin1-p1 not only was required but was
also sufficient for regulation in experiments in vitro. These experiments
also suggested that the pseudogene acts sequence-specifically, affecting
only those genes that show some sequence similarity to itself.
Non-protein-coding RNAs have recently been shown to perform a variety of
tasks, such as gene silencing, catalysis and the regulation of
So Makorin1-p1's mechanism of action might involve its non-coding RNA
product, rather than the pseudogene itself. Hirotsune et al. propose that
this product works to stabilize the Makorin1 mRNA (Fig. 1a). They favour a
model in which the first 700 nucleotides of the Makorin1 mRNA contain a
recognition site for a destabilization factor. Because this 700-nucleotide
domain is shared by the Makorin1-p1 mRNA, the expression of the pseudogene
would provide a means of titrating out the destabilizing factor through
direct competition. In this model, the longer Makorin1 mRNA is unaffected
because its 3' untranslated region protects it from degradation. An
extension of this idea is that Makorin1 self-regulates: it has been
suggested that it encodes an RNA-binding protein6, which might be the
destabilizing factor that downregulates the short form of its own mRNA.
Figure 1 Gene regulation by a pseudogene. Full legend
High resolution image and legend (43k)
Given the available data, however, another mechanism could be at work (Fig.
1b). This is suggested by the fact that mRNA stability is usually
by elements in the 3' untranslated region8 ? rather than at the 5' end,
where the key 700-nucleotide region of Makorin1 is found. The alternative
mechanism would involve the pseudogene DNA locus directly. For example,
perhaps the 700-nucleotide region in the gene and pseudogene contains
elements that, on binding certain proteins, repress transcription. In this
model the repressor proteins would be limited in availability, so that
Makorin1-p1 would compete for repressor binding. These two models ?
RNA-mediated versus DNA-mediated ? have mechanistic differences and could
Whatever the underlying mechanism, the work of Hirotsune et al.5 is
provocative for revealing the first biological function of any pseudogene.
It challenges the popular belief that pseudogenes are simply molecular
fossils ? the evidence of Mother Nature's experiments gone awry. Indeed, it
suggests that evolutionary forces can work in both directions. The forward
direction is driven by pressures to create new genes from existing ones, an
imperfect process that often generates defective copies of the original.
these defective copies need not be evolutionary dead ends, because
in the reverse direction could modify them for specific tasks. In the case
of Makorin1 and Makorin1-p1, the result of bidirectional selection is that
one gene cannot exist without the other ? an example of functional
complicity between a perfected product of evolution and its derivative
castaway. Might the pseudogene copies of other functional genes be
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