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Human-macaque comparisons illuminate variation in neutral substitution rates

BACKGROUND: The evolutionary distance between human and macaque is particularly attractive for investigating local variation in neutral substitution rates, because substitutions can be inferred more reliably than in comparisons with rodents and are less influenced by the effects of current and ancie...

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Autores principales: Tyekucheva, Svitlana, Makova, Kateryna D, Karro, John E, Hardison, Ross C, Miller, Webb, Chiaromonte, Francesca
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2643947/
https://www.ncbi.nlm.nih.gov/pubmed/18447906
http://dx.doi.org/10.1186/gb-2008-9-4-r76
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author Tyekucheva, Svitlana
Makova, Kateryna D
Karro, John E
Hardison, Ross C
Miller, Webb
Chiaromonte, Francesca
author_facet Tyekucheva, Svitlana
Makova, Kateryna D
Karro, John E
Hardison, Ross C
Miller, Webb
Chiaromonte, Francesca
author_sort Tyekucheva, Svitlana
collection PubMed
description BACKGROUND: The evolutionary distance between human and macaque is particularly attractive for investigating local variation in neutral substitution rates, because substitutions can be inferred more reliably than in comparisons with rodents and are less influenced by the effects of current and ancient diversity than in comparisons with closer primates. Here we investigate the human-macaque neutral substitution rate as a function of a number of genomic parameters. RESULTS: Using regression analyses we find that male mutation bias, male (but not female) recombination rate, distance to telomeres and substitution rates computed from orthologous regions in mouse-rat and dog-cow comparisons are prominent predictors of the neutral rate. Additionally, we demonstrate that the previously observed biphasic relationship between neutral rate and GC content can be accounted for by properly combining rates at CpG and non-CpG sites. Finally, we find the neutral rate to be negatively correlated with the densities of several classes of computationally predicted functional elements, and less so with the densities of certain classes of experimentally verified functional elements. CONCLUSION: Our results suggest that while female recombination may be mainly responsible for driving evolution in GC content, male recombination may be mutagenic, and that other mutagenic mechanisms acting near telomeres, and mechanisms whose effects are shared across mammalian genomes, play significant roles. We also have evidence that the nonlinear increase in rates at high GC levels may be largely due to hyper-mutability of CpG dinucleotides. Finally, our results suggest that the performance of conservation-based prediction methods can be improved by accounting for neutral rates.
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spelling pubmed-26439472009-02-17 Human-macaque comparisons illuminate variation in neutral substitution rates Tyekucheva, Svitlana Makova, Kateryna D Karro, John E Hardison, Ross C Miller, Webb Chiaromonte, Francesca Genome Biol Research BACKGROUND: The evolutionary distance between human and macaque is particularly attractive for investigating local variation in neutral substitution rates, because substitutions can be inferred more reliably than in comparisons with rodents and are less influenced by the effects of current and ancient diversity than in comparisons with closer primates. Here we investigate the human-macaque neutral substitution rate as a function of a number of genomic parameters. RESULTS: Using regression analyses we find that male mutation bias, male (but not female) recombination rate, distance to telomeres and substitution rates computed from orthologous regions in mouse-rat and dog-cow comparisons are prominent predictors of the neutral rate. Additionally, we demonstrate that the previously observed biphasic relationship between neutral rate and GC content can be accounted for by properly combining rates at CpG and non-CpG sites. Finally, we find the neutral rate to be negatively correlated with the densities of several classes of computationally predicted functional elements, and less so with the densities of certain classes of experimentally verified functional elements. CONCLUSION: Our results suggest that while female recombination may be mainly responsible for driving evolution in GC content, male recombination may be mutagenic, and that other mutagenic mechanisms acting near telomeres, and mechanisms whose effects are shared across mammalian genomes, play significant roles. We also have evidence that the nonlinear increase in rates at high GC levels may be largely due to hyper-mutability of CpG dinucleotides. Finally, our results suggest that the performance of conservation-based prediction methods can be improved by accounting for neutral rates. BioMed Central 2008-04-30 /pmc/articles/PMC2643947/ /pubmed/18447906 http://dx.doi.org/10.1186/gb-2008-9-4-r76 Text en Copyright © 2008 Tyekucheva et al.; licensee BioMed Central Ltd. https://creativecommons.org/licenses/by/2.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Tyekucheva, Svitlana
Makova, Kateryna D
Karro, John E
Hardison, Ross C
Miller, Webb
Chiaromonte, Francesca
Human-macaque comparisons illuminate variation in neutral substitution rates
title Human-macaque comparisons illuminate variation in neutral substitution rates
title_full Human-macaque comparisons illuminate variation in neutral substitution rates
title_fullStr Human-macaque comparisons illuminate variation in neutral substitution rates
title_full_unstemmed Human-macaque comparisons illuminate variation in neutral substitution rates
title_short Human-macaque comparisons illuminate variation in neutral substitution rates
title_sort human-macaque comparisons illuminate variation in neutral substitution rates
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2643947/
https://www.ncbi.nlm.nih.gov/pubmed/18447906
http://dx.doi.org/10.1186/gb-2008-9-4-r76
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