Both noncoding and protein-coding RNAs contribute to gene expression evolution in the primate brain.

Published online

Journal Article

Despite striking differences in cognition and behavior between humans and our closest primate relatives, several studies have found little evidence for adaptive change in protein-coding regions of genes expressed primarily in the brain. Instead, changes in gene expression may underlie many cognitive and behavioral differences. Here, we used digital gene expression: tag profiling (here called Tag-Seq, also called DGE:tag profiling) to assess changes in global transcript abundance in the frontal cortex of the brains of 3 humans, 3 chimpanzees, and 3 rhesus macaques. A substantial fraction of transcripts we identified as differentially transcribed among species were not assayed in previous studies based on microarrays. Differentially expressed tags within coding regions are enriched for gene functions involved in synaptic transmission, transport, oxidative phosphorylation, and lipid metabolism. Importantly, because Tag-Seq technology provides strand-specific information about all polyadenlyated transcripts, we were able to assay expression in noncoding intragenic regions, including both sense and antisense noncoding transcripts (relative to nearby genes). We find that many noncoding transcripts are conserved in both location and expression level between species, suggesting a possible functional role. Lastly, we examined the overlap between differential gene expression and signatures of positive selection within putative promoter regions, a sign that these differences represent adaptations during human evolution. Comparative approaches may provide important insights into genes responsible for differences in cognitive functions between humans and nonhuman primates, as well as highlighting new candidate genes for studies investigating neurological disorders.

Full Text

Duke Authors

Cited Authors

  • Babbitt, CC; Fedrigo, O; Pfefferle, AD; Boyle, AP; Horvath, JE; Furey, TS; Wray, GA

Published Date

  • January 18, 2010

Published In

Volume / Issue

  • 2 /

Start / End Page

  • 67 - 79

PubMed ID

  • 20333225

Electronic International Standard Serial Number (EISSN)

  • 1759-6653

Digital Object Identifier (DOI)

  • 10.1093/gbe/evq002

Language

  • eng

Conference Location

  • England