Identification of copy number variation in French dairy and beef breeds using next-generation sequencing

Abstract Background Copy number variations (CNV) are known to play a major role in genetic variability and disease pathogenesis in several species including cattle. In this study, we report the identification and characterization of CNV in eight French beef and dairy breeds using whole-genome sequen...

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Main Authors: Rabia Letaief, Emmanuelle Rebours, Cécile Grohs, Cédric Meersseman, Sébastien Fritz, Lidwine Trouilh, Diane Esquerré, Johanna Barbieri, Christophe Klopp, Romain Philippe, Véronique Blanquet, Didier Boichard, Dominique Rocha, Mekki Boussaha
Format: Article
Language:deu
Published: BMC 2017-10-01
Series:Genetics Selection Evolution
Online Access:http://link.springer.com/article/10.1186/s12711-017-0352-z
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spelling doaj-9f283a0c299c433ebbe5fbe4244d3f772020-11-24T23:43:30ZdeuBMCGenetics Selection Evolution1297-96862017-10-0149111510.1186/s12711-017-0352-zIdentification of copy number variation in French dairy and beef breeds using next-generation sequencingRabia Letaief0Emmanuelle Rebours1Cécile Grohs2Cédric Meersseman3Sébastien Fritz4Lidwine Trouilh5Diane Esquerré6Johanna Barbieri7Christophe Klopp8Romain Philippe9Véronique Blanquet10Didier Boichard11Dominique Rocha12Mekki Boussaha13GABI, INRA, AgroParisTech, Université Paris-SaclayGABI, INRA, AgroParisTech, Université Paris-SaclayGABI, INRA, AgroParisTech, Université Paris-SaclayGABI, INRA, AgroParisTech, Université Paris-SaclayGABI, INRA, AgroParisTech, Université Paris-SaclayLISBP, CNRS, INRA, INSA, Université de ToulouseGenPhySE, INRA, Université de Toulouse INPT ENSAT, Université de Toulouse INPT ENVTGenPhySE, INRA, Université de Toulouse INPT ENSAT, Université de Toulouse INPT ENVTSIGENAE, INRAGMA, INRA, Université de Limoges, UMR1061, Unité Génétique Moléculaire AnimaleGMA, INRA, Université de Limoges, UMR1061, Unité Génétique Moléculaire AnimaleGABI, INRA, AgroParisTech, Université Paris-SaclayGABI, INRA, AgroParisTech, Université Paris-SaclayGABI, INRA, AgroParisTech, Université Paris-SaclayAbstract Background Copy number variations (CNV) are known to play a major role in genetic variability and disease pathogenesis in several species including cattle. In this study, we report the identification and characterization of CNV in eight French beef and dairy breeds using whole-genome sequence data from 200 animals. Bioinformatics analyses to search for CNV were carried out using four different but complementary tools and we validated a subset of the CNV by both in silico and experimental approaches. Results We report the identification and localization of 4178 putative deletion-only, duplication-only and CNV regions, which cover 6% of the bovine autosomal genome; they were validated by two in silico approaches and/or experimentally validated using array-based comparative genomic hybridization and single nucleotide polymorphism genotyping arrays. The size of these variants ranged from 334 bp to 7.7 Mb, with an average size of ~ 54 kb. Of these 4178 variants, 3940 were deletions, 67 were duplications and 171 corresponded to both deletions and duplications, which were defined as potential CNV regions. Gene content analysis revealed that, among these variants, 1100 deletions and duplications encompassed 1803 known genes, which affect a wide spectrum of molecular functions, and 1095 overlapped with known QTL regions. Conclusions Our study is a large-scale survey of CNV in eight French dairy and beef breeds. These CNV will be useful to study the link between genetic variability and economically important traits, and to improve our knowledge on the genomic architecture of cattle.http://link.springer.com/article/10.1186/s12711-017-0352-z
collection DOAJ
language deu
format Article
sources DOAJ
author Rabia Letaief
Emmanuelle Rebours
Cécile Grohs
Cédric Meersseman
Sébastien Fritz
Lidwine Trouilh
Diane Esquerré
Johanna Barbieri
Christophe Klopp
Romain Philippe
Véronique Blanquet
Didier Boichard
Dominique Rocha
Mekki Boussaha
spellingShingle Rabia Letaief
Emmanuelle Rebours
Cécile Grohs
Cédric Meersseman
Sébastien Fritz
Lidwine Trouilh
Diane Esquerré
Johanna Barbieri
Christophe Klopp
Romain Philippe
Véronique Blanquet
Didier Boichard
Dominique Rocha
Mekki Boussaha
Identification of copy number variation in French dairy and beef breeds using next-generation sequencing
Genetics Selection Evolution
author_facet Rabia Letaief
Emmanuelle Rebours
Cécile Grohs
Cédric Meersseman
Sébastien Fritz
Lidwine Trouilh
Diane Esquerré
Johanna Barbieri
Christophe Klopp
Romain Philippe
Véronique Blanquet
Didier Boichard
Dominique Rocha
Mekki Boussaha
author_sort Rabia Letaief
title Identification of copy number variation in French dairy and beef breeds using next-generation sequencing
title_short Identification of copy number variation in French dairy and beef breeds using next-generation sequencing
title_full Identification of copy number variation in French dairy and beef breeds using next-generation sequencing
title_fullStr Identification of copy number variation in French dairy and beef breeds using next-generation sequencing
title_full_unstemmed Identification of copy number variation in French dairy and beef breeds using next-generation sequencing
title_sort identification of copy number variation in french dairy and beef breeds using next-generation sequencing
publisher BMC
series Genetics Selection Evolution
issn 1297-9686
publishDate 2017-10-01
description Abstract Background Copy number variations (CNV) are known to play a major role in genetic variability and disease pathogenesis in several species including cattle. In this study, we report the identification and characterization of CNV in eight French beef and dairy breeds using whole-genome sequence data from 200 animals. Bioinformatics analyses to search for CNV were carried out using four different but complementary tools and we validated a subset of the CNV by both in silico and experimental approaches. Results We report the identification and localization of 4178 putative deletion-only, duplication-only and CNV regions, which cover 6% of the bovine autosomal genome; they were validated by two in silico approaches and/or experimentally validated using array-based comparative genomic hybridization and single nucleotide polymorphism genotyping arrays. The size of these variants ranged from 334 bp to 7.7 Mb, with an average size of ~ 54 kb. Of these 4178 variants, 3940 were deletions, 67 were duplications and 171 corresponded to both deletions and duplications, which were defined as potential CNV regions. Gene content analysis revealed that, among these variants, 1100 deletions and duplications encompassed 1803 known genes, which affect a wide spectrum of molecular functions, and 1095 overlapped with known QTL regions. Conclusions Our study is a large-scale survey of CNV in eight French dairy and beef breeds. These CNV will be useful to study the link between genetic variability and economically important traits, and to improve our knowledge on the genomic architecture of cattle.
url http://link.springer.com/article/10.1186/s12711-017-0352-z
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