GENETICS:
Expression of Endorphin Gene Favored in Human Evolution
Michael Balter
Humans and chimpanzees share at least 98% of their DNA sequences. Yet
chimps are an endangered species, whereas humans have used their
superior cognition to transform the face of the earth. What makes the
difference? Thirty years ago, geneticist Mary-Claire King and
biochemist Allan Wilson proposed that changes in how genes are
regulated, rather than in the proteins they code for, was the key (Science, 11 April 1975, p. 107).
A new study of evolutionary changes in the regulation of a gene
implicated in perception, behavior, and memory suggests that King and
Wilson may have been at least partly right.
Other researchers say that the new study is one of the first human
examples of selection acting on a regulatory element, and it adds to a
short list of brain genes now known to have been favored during the
evolution of humans. "The evidence is compelling," says evolutionary
geneticist Bruce Lahn of the University of Chicago. But he and others
note that it is not yet clear what mental or behavioral traits were
favored by selection in this case.
An international team led by evolutionary biologist Gregory Wray of
Duke University in Durham, North Carolina, focused on the gene that
codes for the protein prodynorphin (PDYN), a precursor to a number of
endorphins (opiatelike molecules involved in learning, the experience
of pain, and social attachment and bonding). The PDYN
gene is controlled by a promoter region just upstream from the gene's
coding region. Earlier studies had highlighted a 68 DNA base pair (bp)
segment of the promoter that varies among humans, who carry between one
and four copies of it. It isn't clear how the number of copies and
other variations in the segment affect the gene's function, although
some variants have been linked to schizophrenia, cocaine addiction, and
epilepsy.
Wray and his colleagues sequenced the promoter and some flanking DNA
from 74 human chromosomes as well as 32 chromosomes from seven other
primates, including chimps, gorillas, and orangutans. As the team
reports in the December issue of PloS Biology,
none of the nonhuman primates had more than one copy of the 68-bp
segment. In addition, all human segments had five DNA mutations not
seen in the other primates. The team concludes that the pattern is a
solid example of natural selection acting on the human lineage after it
split from the chimp line about 5 million to 7 million years ago.
Why am I not like him? Differences in gene regulation may help set humans and chimps apart.
CREDIT: JAMES BALOG/GETTY IMAGES |
To see whether the differences in promoters actually altered gene
expression, the team introduced either the chimp or human 68-bp segment
into human neural cells. The human segment induced a 20% greater
expression of the
PDYN gene than did the chimp segment.
The Wray team's work "speaks directly to King and Wilson's hypothesis,"
says molecular biologist Sean Carroll of the University of Wisconsin,
Madison. Carroll adds that the authors have provided a "road map" for
experimental tests of the evolution of gene regulation. Evolutionary
geneticist Svante Pääbo of the Max Planck Institute for Evolutionary
Anthropology in Leipzig, Germany, agrees that the paper provides
"convincing evidence for positive selection." But Pääbo cautions that
this one example does not prove that regulatory mutations were more
important than structural mutations during human evolution.
Because of PDYN's
importance in human biology, the authors suggest that the evolutionary
changes in its regulation may have helped set chimps and humans apart.
But Lahn says that such a conclusion is premature until researchers
know more about why these changes were favored by natural selection.
"It is a bit early to say that these changes were key to what makes us
human," Lahn says. "But it seems like a reasonable hypothesis."