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Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome

For years evolutionary biologists have been interested in searching for the genetic bases underlying humanness. Recent efforts at a large or a complete genomic scale have been conducted to search for positively selected genes in human and in chimp. However, recently developed methods allowing for a...

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Autores principales: Arbiza, Leonardo, Dopazo, Joaquín, Dopazo, Hernán
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1447656/
https://www.ncbi.nlm.nih.gov/pubmed/16683019
http://dx.doi.org/10.1371/journal.pcbi.0020038
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author Arbiza, Leonardo
Dopazo, Joaquín
Dopazo, Hernán
author_facet Arbiza, Leonardo
Dopazo, Joaquín
Dopazo, Hernán
author_sort Arbiza, Leonardo
collection PubMed
description For years evolutionary biologists have been interested in searching for the genetic bases underlying humanness. Recent efforts at a large or a complete genomic scale have been conducted to search for positively selected genes in human and in chimp. However, recently developed methods allowing for a more sensitive and controlled approach in the detection of positive selection can be employed. Here, using 13,198 genes, we have deduced the sets of genes involved in rate acceleration, positive selection, and relaxation of selective constraints in human, in chimp, and in their ancestral lineage since the divergence from murids. Significant deviations from the strict molecular clock were observed in 469 human and in 651 chimp genes. The more stringent branch-site test of positive selection detected 108 human and 577 chimp positively selected genes. An important proportion of the positively selected genes did not show a significant acceleration in rates, and similarly, many of the accelerated genes did not show significant signals of positive selection. Functional differentiation of genes under rate acceleration, positive selection, and relaxation was not statistically significant between human and chimp with the exception of terms related to G-protein coupled receptors and sensory perception. Both of these were over-represented under relaxation in human in relation to chimp. Comparing differences between derived and ancestral lineages, a more conspicuous change in trends seems to have favored positive selection in the human lineage. Since most of the positively selected genes are different under the same functional categories between these species, we suggest that the individual roles of the alternative positively selected genes may be an important factor underlying biological differences between these species.
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spelling pubmed-14476562006-05-08 Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome Arbiza, Leonardo Dopazo, Joaquín Dopazo, Hernán PLoS Comput Biol Research Article For years evolutionary biologists have been interested in searching for the genetic bases underlying humanness. Recent efforts at a large or a complete genomic scale have been conducted to search for positively selected genes in human and in chimp. However, recently developed methods allowing for a more sensitive and controlled approach in the detection of positive selection can be employed. Here, using 13,198 genes, we have deduced the sets of genes involved in rate acceleration, positive selection, and relaxation of selective constraints in human, in chimp, and in their ancestral lineage since the divergence from murids. Significant deviations from the strict molecular clock were observed in 469 human and in 651 chimp genes. The more stringent branch-site test of positive selection detected 108 human and 577 chimp positively selected genes. An important proportion of the positively selected genes did not show a significant acceleration in rates, and similarly, many of the accelerated genes did not show significant signals of positive selection. Functional differentiation of genes under rate acceleration, positive selection, and relaxation was not statistically significant between human and chimp with the exception of terms related to G-protein coupled receptors and sensory perception. Both of these were over-represented under relaxation in human in relation to chimp. Comparing differences between derived and ancestral lineages, a more conspicuous change in trends seems to have favored positive selection in the human lineage. Since most of the positively selected genes are different under the same functional categories between these species, we suggest that the individual roles of the alternative positively selected genes may be an important factor underlying biological differences between these species. Public Library of Science 2006-04 2006-04-28 /pmc/articles/PMC1447656/ /pubmed/16683019 http://dx.doi.org/10.1371/journal.pcbi.0020038 Text en © 2006 Arbiza et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Arbiza, Leonardo
Dopazo, Joaquín
Dopazo, Hernán
Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome
title Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome
title_full Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome
title_fullStr Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome
title_full_unstemmed Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome
title_short Positive Selection, Relaxation, and Acceleration in the Evolution of the Human and Chimp Genome
title_sort positive selection, relaxation, and acceleration in the evolution of the human and chimp genome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1447656/
https://www.ncbi.nlm.nih.gov/pubmed/16683019
http://dx.doi.org/10.1371/journal.pcbi.0020038
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