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Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing
BACKGROUND: Whole genome re-sequencing data from dogs and wolves are now commonly used to study how natural and artificial selection have shaped the patterns of genetic diversity. Single nucleotide polymorphisms, microsatellites and variants in mitochondrial DNA have been interrogated for links to s...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735816/ https://www.ncbi.nlm.nih.gov/pubmed/29258433 http://dx.doi.org/10.1186/s12864-017-4318-x |
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author | Serres-Armero, Aitor Povolotskaya, Inna S. Quilez, Javier Ramirez, Oscar Santpere, Gabriel Kuderna, Lukas F. K. Hernandez-Rodriguez, Jessica Fernandez-Callejo, Marcos Gomez-Sanchez, Daniel Freedman, Adam H. Fan, Zhenxin Novembre, John Navarro, Arcadi Boyko, Adam Wayne, Robert Vilà, Carles Lorente-Galdos, Belen Marques-Bonet, Tomas |
author_facet | Serres-Armero, Aitor Povolotskaya, Inna S. Quilez, Javier Ramirez, Oscar Santpere, Gabriel Kuderna, Lukas F. K. Hernandez-Rodriguez, Jessica Fernandez-Callejo, Marcos Gomez-Sanchez, Daniel Freedman, Adam H. Fan, Zhenxin Novembre, John Navarro, Arcadi Boyko, Adam Wayne, Robert Vilà, Carles Lorente-Galdos, Belen Marques-Bonet, Tomas |
author_sort | Serres-Armero, Aitor |
collection | PubMed |
description | BACKGROUND: Whole genome re-sequencing data from dogs and wolves are now commonly used to study how natural and artificial selection have shaped the patterns of genetic diversity. Single nucleotide polymorphisms, microsatellites and variants in mitochondrial DNA have been interrogated for links to specific phenotypes or signals of domestication. However, copy number variation (CNV), despite its increasingly recognized importance as a contributor to phenotypic diversity, has not been extensively explored in canids. RESULTS: Here, we develop a new accurate probabilistic framework to create fine-scale genomic maps of segmental duplications (SDs), compare patterns of CNV across groups and investigate their role in the evolution of the domestic dog by using information from 34 canine genomes. Our analyses show that duplicated regions are enriched in genes and hence likely possess functional importance. We identify 86 loci with large CNV differences between dogs and wolves, enriched in genes responsible for sensory perception, immune response, metabolic processes, etc. In striking contrast to the observed loss of nucleotide diversity in domestic dogs following the population bottlenecks that occurred during domestication and breed creation, we find a similar proportion of CNV loci in dogs and wolves, suggesting that other dynamics are acting to particularly select for CNVs with potentially functional impacts. CONCLUSIONS: This work is the first comparison of genome wide CNV patterns in domestic and wild canids using whole-genome sequencing data and our findings contribute to study the impact of novel kinds of genetic changes on the evolution of the domestic dog. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-4318-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5735816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57358162017-12-21 Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing Serres-Armero, Aitor Povolotskaya, Inna S. Quilez, Javier Ramirez, Oscar Santpere, Gabriel Kuderna, Lukas F. K. Hernandez-Rodriguez, Jessica Fernandez-Callejo, Marcos Gomez-Sanchez, Daniel Freedman, Adam H. Fan, Zhenxin Novembre, John Navarro, Arcadi Boyko, Adam Wayne, Robert Vilà, Carles Lorente-Galdos, Belen Marques-Bonet, Tomas BMC Genomics Research Article BACKGROUND: Whole genome re-sequencing data from dogs and wolves are now commonly used to study how natural and artificial selection have shaped the patterns of genetic diversity. Single nucleotide polymorphisms, microsatellites and variants in mitochondrial DNA have been interrogated for links to specific phenotypes or signals of domestication. However, copy number variation (CNV), despite its increasingly recognized importance as a contributor to phenotypic diversity, has not been extensively explored in canids. RESULTS: Here, we develop a new accurate probabilistic framework to create fine-scale genomic maps of segmental duplications (SDs), compare patterns of CNV across groups and investigate their role in the evolution of the domestic dog by using information from 34 canine genomes. Our analyses show that duplicated regions are enriched in genes and hence likely possess functional importance. We identify 86 loci with large CNV differences between dogs and wolves, enriched in genes responsible for sensory perception, immune response, metabolic processes, etc. In striking contrast to the observed loss of nucleotide diversity in domestic dogs following the population bottlenecks that occurred during domestication and breed creation, we find a similar proportion of CNV loci in dogs and wolves, suggesting that other dynamics are acting to particularly select for CNVs with potentially functional impacts. CONCLUSIONS: This work is the first comparison of genome wide CNV patterns in domestic and wild canids using whole-genome sequencing data and our findings contribute to study the impact of novel kinds of genetic changes on the evolution of the domestic dog. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-4318-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-19 /pmc/articles/PMC5735816/ /pubmed/29258433 http://dx.doi.org/10.1186/s12864-017-4318-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Serres-Armero, Aitor Povolotskaya, Inna S. Quilez, Javier Ramirez, Oscar Santpere, Gabriel Kuderna, Lukas F. K. Hernandez-Rodriguez, Jessica Fernandez-Callejo, Marcos Gomez-Sanchez, Daniel Freedman, Adam H. Fan, Zhenxin Novembre, John Navarro, Arcadi Boyko, Adam Wayne, Robert Vilà, Carles Lorente-Galdos, Belen Marques-Bonet, Tomas Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing |
title | Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing |
title_full | Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing |
title_fullStr | Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing |
title_full_unstemmed | Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing |
title_short | Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing |
title_sort | similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735816/ https://www.ncbi.nlm.nih.gov/pubmed/29258433 http://dx.doi.org/10.1186/s12864-017-4318-x |
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