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Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain
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...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839352/ https://www.ncbi.nlm.nih.gov/pubmed/20333225 http://dx.doi.org/10.1093/gbe/evq002 |
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author | Babbitt, Courtney C. Fedrigo, Olivier Pfefferle, Adam D. Boyle, Alan P. Horvath, Julie E. Furey, Terrence S. Wray, Gregory A. |
author_facet | Babbitt, Courtney C. Fedrigo, Olivier Pfefferle, Adam D. Boyle, Alan P. Horvath, Julie E. Furey, Terrence S. Wray, Gregory A. |
author_sort | Babbitt, Courtney C. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2839352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28393522010-03-22 Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain Babbitt, Courtney C. Fedrigo, Olivier Pfefferle, Adam D. Boyle, Alan P. Horvath, Julie E. Furey, Terrence S. Wray, Gregory A. Genome Biol Evol Research Articles 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. Oxford University Press 2010 2010-01-18 /pmc/articles/PMC2839352/ /pubmed/20333225 http://dx.doi.org/10.1093/gbe/evq002 Text en © The Author(s) 2010. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Babbitt, Courtney C. Fedrigo, Olivier Pfefferle, Adam D. Boyle, Alan P. Horvath, Julie E. Furey, Terrence S. Wray, Gregory A. Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain |
title | Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain |
title_full | Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain |
title_fullStr | Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain |
title_full_unstemmed | Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain |
title_short | Both Noncoding and Protein-Coding RNAs Contribute to Gene Expression Evolution in the Primate Brain |
title_sort | both noncoding and protein-coding rnas contribute to gene expression evolution in the primate brain |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839352/ https://www.ncbi.nlm.nih.gov/pubmed/20333225 http://dx.doi.org/10.1093/gbe/evq002 |
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