Small genetic mutations that add up over time could create an evolutionary express lane that leads to the rapid development of new traits, researchers from the University of Pittsburgh and the University of Wisconsin at Madison have found.
The team reports in the Proceedings of the National Academy of Sciences (PNAS) that slight changes in segments of DNA known as transcriptional enhancerswhich determine the when, where, and how much in gene productioncan activate dormant genetic imperfections. These alterations awaken specific genes to low-level activity, or "leakiness," in developing tissue different from the genes' typical location. Just a few subsequent mutations build on that stirring to result in a new function for an old geneand possibly a novel trait.
Coauthor Mark Rebeiz [Ra-BAYS], a professor of biological sciences in Pitt's School of Arts and Sciences, and his colleagues traced how a certain unwitting gene found itself in the unique optical neurons of a species of fruit fly. They found that tiny alterations in the transcriptional enhancers of the species' ancestor caused the gene to take root in these neurons for the first time. A couple of mutations later and the gene became a permanent fixture in the fly's brain cells. Rebeiz worked with coauthors Sean Carroll, professor of molecular biology and genetics at the UW-Madison; Nick Jikomes, an undergraduate researcher in Carroll's laboratory; and Victoria Kassner, a research associate in Carroll's lab.
The Pitt-UW Madison work expands on research during the past 30 years demonstrating that new genes made from scratch are rare in animals, Rebeiz said. Instead, the diversity of living things is thought to stem from existing genes showing up in new locations. In a famous example of the lack of originality in animal genes, researchers at the University of Basel in Switzerland reported in Science in 1995 that a gene known as PAX6, a "master control" gene for the formation of eyes and other features in flies, mice, and humans, could cause the growth of additional eyes on the legs and antennae of fruit flies.
With their report in PNAS, Rebeiz and his coauthors offer the first explanation of what makes these genes go astray in the first placeand they identified the deviant DNA as the culprit.
The researchers found that the gene Neprilysin-1 present in the optical neurons of the fruit fly species Drosophilia santomea emerged in that location about 400,000 years agoa blip in evolutionary termsin the last common ancestor the fly shared with its relative D. yakuba. The mutation began with a transcriptional enhancer for the gene, which caused Neprilysin-1 to show up in different neurons than usual.
From there, Rebeiz said, the development of D. santomea's distinguishing neurons plays out with the clarity of a film as four mutations in subsequent generations intensify the errant enhancer's impact until Neprilysin-1's presence in optical neurons become an exclusive feature of D. santomea. On the other hand, ensuing genetic alterations in D. yakuba actually extinguished this new expression and restored that fly's Neprilysin-1 to its original location.
"It has been long appreciated that nature doesn't make anything from scratch, but the mystery has remained of how genes that have been performing the same job for hundreds of millions of years are suddenly expressed in new places," Rebeiz said. "Our work shows that even slight mutations in a transcriptional enhancer can cause leaky gene activity, which can initiate a short route to the development of new traits."
Explore further: Automating the selection process for a genome assembler