TY - JOUR
T1 - Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping
AU - Vaysse, Amaury
AU - Ratnakumar, Abhirami
AU - Derrien, Thomas
AU - Axelsson, Erik
AU - Pielberg, Gerli Rosengren
AU - Sigurdsson, Snaevar
AU - Fall, Tove
AU - Seppälä, Eija H.
AU - Hansen, Mark S.T.
AU - Lawley, Cindy T.
AU - Karlsson, Elinor K.
AU - Bannasch, Danika
AU - Vilà, Carles
AU - Lohi, Hannes
AU - Galibert, Francis
AU - Fredholm, Merete
AU - Häggström, Jens
AU - Hedhammar, Åke
AU - André, Catherine
AU - Lindblad-Toh, Kerstin
AU - Hitte, Christophe
AU - Webster, Matthew T.
PY - 2011/10
Y1 - 2011/10
N2 - The extraordinary phenotypic diversity of dog breeds has been sculpted by a unique population history accompanied by selection for novel and desirable traits. Here we perform a comprehensive analysis using multiple test statistics to identify regions under selection in 509 dogs from 46 diverse breeds using a newly developed high-density genotyping array consisting of >170,000 evenly spaced SNPs. We first identify 44 genomic regions exhibiting extreme differentiation across multiple breeds. Genetic variation in these regions correlates with variation in several phenotypic traits that vary between breeds, and we identify novel associations with both morphological and behavioral traits. We next scan the genome for signatures of selective sweeps in single breeds, characterized by long regions of reduced heterozygosity and fixation of extended haplotypes. These scans identify hundreds of regions, including 22 blocks of homozygosity longer than one megabase in certain breeds. Candidate selection loci are strongly enriched for developmental genes. We chose one highly differentiated region, associated with body size and ear morphology, and characterized it using high-throughput sequencing to provide a list of variants that may directly affect these traits. This study provides a catalogue of genomic regions showing extreme reduction in genetic variation or population differentiation in dogs, including many linked to phenotypic variation. The many blocks of reduced haplotype diversity observed across the genome in dog breeds are the result of both selection and genetic drift, but extended blocks of homozygosity on a megabase scale appear to be best explained by selection. Further elucidation of the variants under selection will help to uncover the genetic basis of complex traits and disease.
AB - The extraordinary phenotypic diversity of dog breeds has been sculpted by a unique population history accompanied by selection for novel and desirable traits. Here we perform a comprehensive analysis using multiple test statistics to identify regions under selection in 509 dogs from 46 diverse breeds using a newly developed high-density genotyping array consisting of >170,000 evenly spaced SNPs. We first identify 44 genomic regions exhibiting extreme differentiation across multiple breeds. Genetic variation in these regions correlates with variation in several phenotypic traits that vary between breeds, and we identify novel associations with both morphological and behavioral traits. We next scan the genome for signatures of selective sweeps in single breeds, characterized by long regions of reduced heterozygosity and fixation of extended haplotypes. These scans identify hundreds of regions, including 22 blocks of homozygosity longer than one megabase in certain breeds. Candidate selection loci are strongly enriched for developmental genes. We chose one highly differentiated region, associated with body size and ear morphology, and characterized it using high-throughput sequencing to provide a list of variants that may directly affect these traits. This study provides a catalogue of genomic regions showing extreme reduction in genetic variation or population differentiation in dogs, including many linked to phenotypic variation. The many blocks of reduced haplotype diversity observed across the genome in dog breeds are the result of both selection and genetic drift, but extended blocks of homozygosity on a megabase scale appear to be best explained by selection. Further elucidation of the variants under selection will help to uncover the genetic basis of complex traits and disease.
UR - http://www.scopus.com/inward/record.url?scp=80055088614&partnerID=8YFLogxK
U2 - 10.1371/journal.pgen.1002316
DO - 10.1371/journal.pgen.1002316
M3 - Article
C2 - 22022279
AN - SCOPUS:80055088614
SN - 1553-7390
VL - 7
JO - PLoS Genetics
JF - PLoS Genetics
IS - 10
M1 - e1002316
ER -