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Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection
BACKGROUND: Copy number variants (CNVs), defined as losses and gains of segments of genomic DNA, are a major source of genomic variation. RESULTS: In this study, we identified over 2,000 human CNVs that overlap with orthologous chimpanzee or orthologous macaque CNVs. Of these, 170 CNVs overlap with...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219974/ https://www.ncbi.nlm.nih.gov/pubmed/21627829 http://dx.doi.org/10.1186/gb-2011-12-5-r52 |
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author | Gokcumen, Omer Babb, Paul L Iskow, Rebecca C Zhu, Qihui Shi, Xinghua Mills, Ryan E Ionita-Laza, Iuliana Vallender, Eric J Clark, Andrew G Johnson, Welkin E Lee, Charles |
author_facet | Gokcumen, Omer Babb, Paul L Iskow, Rebecca C Zhu, Qihui Shi, Xinghua Mills, Ryan E Ionita-Laza, Iuliana Vallender, Eric J Clark, Andrew G Johnson, Welkin E Lee, Charles |
author_sort | Gokcumen, Omer |
collection | PubMed |
description | BACKGROUND: Copy number variants (CNVs), defined as losses and gains of segments of genomic DNA, are a major source of genomic variation. RESULTS: In this study, we identified over 2,000 human CNVs that overlap with orthologous chimpanzee or orthologous macaque CNVs. Of these, 170 CNVs overlap with both chimpanzee and macaque CNVs, and these were collapsed into 34 hotspot regions of CNV formation. Many of these hotspot regions of CNV formation are functionally relevant, with a bias toward genes involved in immune function, some of which were previously shown to evolve under balancing selection in humans. The genes in these primate CNV formation hotspots have significant differential expression levels between species and show evidence for positive selection, indicating that they have evolved under species-specific, directional selection. CONCLUSIONS: These hotspots of primate CNV formation provide a novel perspective on divergence and selective pressures acting on these genomic regions. |
format | Online Article Text |
id | pubmed-3219974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32199742012-05-31 Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection Gokcumen, Omer Babb, Paul L Iskow, Rebecca C Zhu, Qihui Shi, Xinghua Mills, Ryan E Ionita-Laza, Iuliana Vallender, Eric J Clark, Andrew G Johnson, Welkin E Lee, Charles Genome Biol Research BACKGROUND: Copy number variants (CNVs), defined as losses and gains of segments of genomic DNA, are a major source of genomic variation. RESULTS: In this study, we identified over 2,000 human CNVs that overlap with orthologous chimpanzee or orthologous macaque CNVs. Of these, 170 CNVs overlap with both chimpanzee and macaque CNVs, and these were collapsed into 34 hotspot regions of CNV formation. Many of these hotspot regions of CNV formation are functionally relevant, with a bias toward genes involved in immune function, some of which were previously shown to evolve under balancing selection in humans. The genes in these primate CNV formation hotspots have significant differential expression levels between species and show evidence for positive selection, indicating that they have evolved under species-specific, directional selection. CONCLUSIONS: These hotspots of primate CNV formation provide a novel perspective on divergence and selective pressures acting on these genomic regions. BioMed Central 2011 2011-05-31 /pmc/articles/PMC3219974/ /pubmed/21627829 http://dx.doi.org/10.1186/gb-2011-12-5-r52 Text en Copyright ©2011 Gokcumen O et al.; licensee BioMed Central Ltd http://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), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Gokcumen, Omer Babb, Paul L Iskow, Rebecca C Zhu, Qihui Shi, Xinghua Mills, Ryan E Ionita-Laza, Iuliana Vallender, Eric J Clark, Andrew G Johnson, Welkin E Lee, Charles Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection |
title | Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection |
title_full | Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection |
title_fullStr | Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection |
title_full_unstemmed | Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection |
title_short | Refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection |
title_sort | refinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219974/ https://www.ncbi.nlm.nih.gov/pubmed/21627829 http://dx.doi.org/10.1186/gb-2011-12-5-r52 |
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