Strong signatures of selection in the domestic pig genome

生物 驯化 外套 非同义代换 遗传学 基因座(遗传学) 家猪 选择性扫描 等位基因 进化生物学 数量性状位点 单倍型 基因组 选择(遗传算法) 性状 定向选择 否定选择 表型 基因 遗传变异 人工智能 古生物学 林业 地理 计算机科学
作者
Carl‐Johan Rubin,Hendrik‐Jan Megens,Álvaro Martínez Barrio,Khurram Maqbool,Shumaila Sayyab,Doreen Schwochow,Chao Wang,Örjan Carlborg,Patric Jern,Claus B. Jørgensen,Alan Archibald,Merete Fredholm,Martien A. M. Groenen,Leif Andersson
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:109 (48): 19529-19536 被引量:586
标识
DOI:10.1073/pnas.1217149109
摘要

Domestication of wild boar ( Sus scrofa ) and subsequent selection have resulted in dramatic phenotypic changes in domestic pigs for a number of traits, including behavior, body composition, reproduction, and coat color. Here we have used whole-genome resequencing to reveal some of the loci that underlie phenotypic evolution in European domestic pigs. Selective sweep analyses revealed strong signatures of selection at three loci harboring quantitative trait loci that explain a considerable part of one of the most characteristic morphological changes in the domestic pig—the elongation of the back and an increased number of vertebrae. The three loci were associated with the NR6A1, PLAG1 , and LCORL genes. The latter two have repeatedly been associated with loci controlling stature in other domestic animals and in humans. Most European domestic pigs are homozygous for the same haplotype at these three loci. We found an excess of derived nonsynonymous substitutions in domestic pigs, most likely reflecting both positive selection and relaxed purifying selection after domestication. Our analysis of structural variation revealed four duplications at the KIT locus that were exclusively present in white or white-spotted pigs, carrying the Dominant white , Patch , or Belt alleles. This discovery illustrates how structural changes have contributed to rapid phenotypic evolution in domestic animals and how alleles in domestic animals may evolve by the accumulation of multiple causative mutations as a response to strong directional selection.

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