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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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