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http://acervodigital.unesp.br/handle/11449/74246
- Title:
- Genome-Wide Analysis Reveals Selection for Important Traits in Domestic Horse Breeds
- Petersen, Jessica L.
- Mickelson, James R.
- Rendahl, Aaron K.
- Valberg, Stephanie J.
- Andersson, Lisa S.
- Axelsson, Jeanette
- Bailey, Ernie
- Bannasch, Danika
- Binns, Matthew M.
- Borges, Alexandre Secorun
- Brama, Pieter
- da Câmara Machado, Artur
- Capomaccio, Stefano
- Cappelli, Katia
- Cothran, E. Gus
- Distl, Ottmar
- Fox-Clipsham, Laura
- Graves, Kathryn T.
- Guérin, Gérard
- Haase, Bianca
- Hasegawa, Telhisa
- Hemmann, Karin
- Hill, Emmeline W.
- Leeb, Tosso
- Lindgren, Gabriella
- Lohi, Hannes
- Lopes, Maria Susana
- McGivney, Beatrice A.
- Mikko, Sofia
- Orr, Nicholas
- Penedo, M. Cecilia T.
- Piercy, Richard J.
- Raekallio, Marja
- Rieder, Stefan
- Røed, Knut H.
- Swinburne, June
- Tozaki, Teruaki
- Vaudin, Mark
- Wade, Claire M.
- McCue, Molly E.
- University of Minnesota
- Swedish University of Agricultural Sciences
- University of Kentucky
- University of California Davis
- Equine Analysis
- Universidade Estadual Paulista (UNESP)
- University College Dublin
- University of the Azores
- University of Perugia
- Texas AandM University
- University of Veterinary Medicine Hannover
- Animal Health Trust
- French National Institute for Agricultural Research
- University of Sydney
- Nihon Bioresource College
- University of Helsinki
- University of Bern
- Institute of Cancer Research
- Royal Veterinary College
- Agroscope Liebefeld-Posieux Research Station
- Norwegian School of Veterinary Science
- Animal DNA Diagnostics
- Laboratory of Racing Chemistry
- 1553-7390
- 1553-7404
- Intense selective pressures applied over short evolutionary time have resulted in homogeneity within, but substantial variation among, horse breeds. Utilizing this population structure, 744 individuals from 33 breeds, and a 54,000 SNP genotyping array, breed-specific targets of selection were identified using an FST-based statistic calculated in 500-kb windows across the genome. A 5.5-Mb region of ECA18, in which the myostatin (MSTN) gene was centered, contained the highest signature of selection in both the Paint and Quarter Horse. Gene sequencing and histological analysis of gluteal muscle biopsies showed a promoter variant and intronic SNP of MSTN were each significantly associated with higher Type 2B and lower Type 1 muscle fiber proportions in the Quarter Horse, demonstrating a functional consequence of selection at this locus. Signatures of selection on ECA23 in all gaited breeds in the sample led to the identification of a shared, 186-kb haplotype including two doublesex related mab transcription factor genes (DMRT2 and 3). The recent identification of a DMRT3 mutation within this haplotype, which appears necessary for the ability to perform alternative gaits, provides further evidence for selection at this locus. Finally, putative loci for the determination of size were identified in the draft breeds and the Miniature horse on ECA11, as well as when signatures of selection surrounding candidate genes at other loci were examined. This work provides further evidence of the importance of MSTN in racing breeds, provides strong evidence for selection upon gait and size, and illustrates the potential for population-based techniques to find genomic regions driving important phenotypes in the modern horse. © 2013 Petersen et al.
- 1-Jan-2013
- PLoS Genetics, v. 9, n. 1, 2013.
- myostatin
- breed
- DMRT2 gene
- DMRT3 gene
- domestic animal
- gait
- gene
- gene locus
- gene sequence
- genetic association
- genetic selection
- genetic trait
- genetic variability
- genome
- gluteus maximus muscle
- haplotype
- heterozygosity
- histology
- homozygosity
- horse
- intron
- MSTN gene
- muscle biopsy
- muscle cell
- nonhuman
- phenotype
- population structure
- promoter region
- sample size
- single nucleotide polymorphism
- Animals
- Biological Evolution
- Breeding
- Genome-Wide Association Study
- Genotype
- Haplotypes
- Horses
- Myostatin
- Phenotype
- Polymorphism, Single Nucleotide
- Selection, Genetic
- http://dx.doi.org/10.1371/journal.pgen.1003211
- Acesso aberto
- outro
- http://repositorio.unesp.br/handle/11449/74246
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