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Derived variants at six genes explain nearly half of size reduction in dog breeds

Selective breeding of dogs by humans has generated extraordinary diversity in body size. A number of multibreed analyses have been undertaken to identify the genetic basis of this diversity. We analyzed four loci discovered in a previous genome-wide association study that used 60,968 SNPs to identif...

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Autores principales: Rimbault, Maud, Beale, Holly C., Schoenebeck, Jeffrey J., Hoopes, Barbara C., Allen, Jeremy J., Kilroy-Glynn, Paul, Wayne, Robert K., Sutter, Nathan B., Ostrander, Elaine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847769/
https://www.ncbi.nlm.nih.gov/pubmed/24026177
http://dx.doi.org/10.1101/gr.157339.113
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author Rimbault, Maud
Beale, Holly C.
Schoenebeck, Jeffrey J.
Hoopes, Barbara C.
Allen, Jeremy J.
Kilroy-Glynn, Paul
Wayne, Robert K.
Sutter, Nathan B.
Ostrander, Elaine A.
author_facet Rimbault, Maud
Beale, Holly C.
Schoenebeck, Jeffrey J.
Hoopes, Barbara C.
Allen, Jeremy J.
Kilroy-Glynn, Paul
Wayne, Robert K.
Sutter, Nathan B.
Ostrander, Elaine A.
author_sort Rimbault, Maud
collection PubMed
description Selective breeding of dogs by humans has generated extraordinary diversity in body size. A number of multibreed analyses have been undertaken to identify the genetic basis of this diversity. We analyzed four loci discovered in a previous genome-wide association study that used 60,968 SNPs to identify size-associated genomic intervals, which were too large to assign causative roles to genes. First, we performed fine-mapping to define critical intervals that included the candidate genes GHR, HMGA2, SMAD2, and STC2, identifying five highly associated markers at the four loci. We hypothesize that three of the variants are likely to be causative. We then genotyped each marker, together with previously reported size-associated variants in the IGF1 and IGF1R genes, on a panel of 500 domestic dogs from 93 breeds, and identified the ancestral allele by genotyping the same markers on 30 wild canids. We observed that the derived alleles at all markers correlated with reduced body size, and smaller dogs are more likely to carry derived alleles at multiple markers. However, breeds are not generally fixed at all markers; multiple combinations of genotypes are found within most breeds. Finally, we show that 46%–52.5% of the variance in body size of dog breeds can be explained by seven markers in proximity to exceptional candidate genes. Among breeds with standard weights <41 kg (90 lb), the genotypes accounted for 64.3% of variance in weight. This work advances our understanding of mammalian growth by describing genetic contributions to canine size determination in non-giant dog breeds.
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spelling pubmed-38477692013-12-10 Derived variants at six genes explain nearly half of size reduction in dog breeds Rimbault, Maud Beale, Holly C. Schoenebeck, Jeffrey J. Hoopes, Barbara C. Allen, Jeremy J. Kilroy-Glynn, Paul Wayne, Robert K. Sutter, Nathan B. Ostrander, Elaine A. Genome Res Research Selective breeding of dogs by humans has generated extraordinary diversity in body size. A number of multibreed analyses have been undertaken to identify the genetic basis of this diversity. We analyzed four loci discovered in a previous genome-wide association study that used 60,968 SNPs to identify size-associated genomic intervals, which were too large to assign causative roles to genes. First, we performed fine-mapping to define critical intervals that included the candidate genes GHR, HMGA2, SMAD2, and STC2, identifying five highly associated markers at the four loci. We hypothesize that three of the variants are likely to be causative. We then genotyped each marker, together with previously reported size-associated variants in the IGF1 and IGF1R genes, on a panel of 500 domestic dogs from 93 breeds, and identified the ancestral allele by genotyping the same markers on 30 wild canids. We observed that the derived alleles at all markers correlated with reduced body size, and smaller dogs are more likely to carry derived alleles at multiple markers. However, breeds are not generally fixed at all markers; multiple combinations of genotypes are found within most breeds. Finally, we show that 46%–52.5% of the variance in body size of dog breeds can be explained by seven markers in proximity to exceptional candidate genes. Among breeds with standard weights <41 kg (90 lb), the genotypes accounted for 64.3% of variance in weight. This work advances our understanding of mammalian growth by describing genetic contributions to canine size determination in non-giant dog breeds. Cold Spring Harbor Laboratory Press 2013-12 /pmc/articles/PMC3847769/ /pubmed/24026177 http://dx.doi.org/10.1101/gr.157339.113 Text en © 2013 Rimbault et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Research
Rimbault, Maud
Beale, Holly C.
Schoenebeck, Jeffrey J.
Hoopes, Barbara C.
Allen, Jeremy J.
Kilroy-Glynn, Paul
Wayne, Robert K.
Sutter, Nathan B.
Ostrander, Elaine A.
Derived variants at six genes explain nearly half of size reduction in dog breeds
title Derived variants at six genes explain nearly half of size reduction in dog breeds
title_full Derived variants at six genes explain nearly half of size reduction in dog breeds
title_fullStr Derived variants at six genes explain nearly half of size reduction in dog breeds
title_full_unstemmed Derived variants at six genes explain nearly half of size reduction in dog breeds
title_short Derived variants at six genes explain nearly half of size reduction in dog breeds
title_sort derived variants at six genes explain nearly half of size reduction in dog breeds
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847769/
https://www.ncbi.nlm.nih.gov/pubmed/24026177
http://dx.doi.org/10.1101/gr.157339.113
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