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Genome-Wide Association Study Identifies Two Major Loci Affecting Calving Ease and Growth-Related Traits in Cattle

机译:全基因组关联研究确定了两个主要基因座影响着牛的产犊缓解和与生长相关的性状

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摘要

Identifying quantitative trait loci (QTL) underlying complex, low-heritability traits is notoriously difficult. Prototypical for such traits, calving ease is an important breeding objective of cattle (Bos taurus)-improving programs. To identify QTL underlying calving ease, we performed a genome-wide association study using estimated breeding values (EBVs) as highly heritable phenotypes for paternal calving ease (pCE) and related traits. The massively structured study population consisted of 1800 bulls of the German Fleckvieh (FV) breed. Two pCE-associated regions on bovine chromosomes (BTA) 14 and 21 (P = 5.72 × 10−15 and P = 2.27 × 10−8, respectively) were identified using principal components analysis to correct for population stratification. The two most significantly associated SNPs explain 10% of the EBV variation. Since marker alleles with negative effect on pCE have positive effects on growth-related traits, the QTL may exert their effects on the birthing process through fetal growth traits. The QTL region on BTA14 corresponds to a human chromosome (HSA) region that is associated with growth characteristics. The HSA region corresponding to the BTA21 pCE QTL is maternally imprinted and involved in the Prader–Willi and Angelman syndromes. Resequencing of positional candidate genes on BTA14 revealed a highly significantly (P = 1.96 × 10−14) associated polymorphism ablating a polyadenylation signal of the gene encoding ribosomal protein S20 (RPS20). Our study demonstrates the leverage potential of EBVs in unraveling the genetic architecture of lowly heritable traits.
机译:众所周知,确定复杂的,低遗传力的特质背后的数量性状基因座(QTL)非常困难。这种特性的典型代表是,产犊容易是牛(Bos taurus)改良计划的重要育种目标。为了确定潜在的产犊难易性的QTL,我们进行了全基因组关联研究,使用估计的育种值(EBV)作为父系产犊难易性(pCE)和相关性状的高度遗传表型。结构庞大的研究种群由1800头德国Fleckvieh(FV)品种的公牛组成。使用以下方法鉴定了牛染色体(BTA)14和21上的两个pCE相关区域(分别为P = 5.72×10 -15 和P = 2.27×10 -8 )。主成分分析以校正人口分层。两个最相关的SNP解释了EBV变异的10%。由于对pCE具有负面影响的标记等位基因对与生长相关的性状具有积极影响,因此QTL可能通过胎儿的生长性状对生育过程产生影响。 BTA14上的QTL区域对应于与生长特性相关的人类染色体(HSA)区域。对应于BTA21 pCE QTL的HSA区域具有母性印记,并参与了Prader-Willi和Angelman综合征。 BTA14上的位置候选基因的重测序显示出高度显着(P = 1.96×10 −14 )相关的多态性,消除了核糖体蛋白S20(RPS20)编码基因的多腺苷酸化信号。我们的研究表明,EBV在揭示低遗传性状的遗传结构方面具有潜在的杠杆作用。

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