GenSys Associated Consultants, Porto Alegre, Rio Grande do Sul, Brazil.
Department of Animal Sciences, School of Agricultural and Veterinary Sciences, São Paulo State University (UNESP), Jaboticabal, São Paulo, Brazil.
PLoS One. 2019 Jan 24;14(1):e0211159. doi: 10.1371/journal.pone.0211159. eCollection 2019.
Reproductive performance is a key indicator of the long-term sustainability of any livestock production system. Testicular hypoplasia (TH) is a morphological and functional reproductive disorder that affects bulls around the world and consequently causes major economic losses due to reduced fertility rates. Despite the improvements in management practices to enhance performance of affected animals, the use of hypoplastic animals for reproduction might contribute to expand the prevalence of this disorder. The aim of this study was to identify genomic regions that are associated with TH in Nellore cattle by performing a genome-wide association study (GWAS) and functional analyses. Phenotypic and pedigree data from 47,563 animals and genotypes (500,689 Single Nucleotide Polymorphism, SNPs) from 265 sires were used in this study. TH was evaluated as a binary trait measured at 18 months of age. The estimated breeding values (EBVs) were calculated by fitting a single-trait threshold animal model using a Bayesian approach. The SNP effects were estimated using the Bayes C method and de-regressed EBVs for TH as the response variable (pseudo-phenotype). The top-15 ranking windows (5-adjacent SNPs) that explained the highest proportion of variance were identified for further functional and biological network analyses. The posterior mean (95% highest posterior density) of the heritability for TH was 0.16 (0.08; 0.23). The most important genomic windows were located on BTA1, BTA3, BTA4, BTA5, BTA9, BTA22, BTA23, and BTA25. These windows explained together 22.69% of the total additive genetic variance for TH. Strong candidate genes associated with metabolism and synthesis of steroids, cell survival, spermatogenesis process and sperm motility were identified, which might play an important role in the expression of TH. Our findings contribute to a better biological understanding of TH and future characterization of causal variants might enable improved genomic prediction of this trait in beef cattle.
繁殖性能是任何家畜生产系统长期可持续性的关键指标。睾丸发育不全(TH)是一种影响全球公牛的形态和功能生殖障碍,因此由于降低了繁殖率而导致重大经济损失。尽管采取了改进管理实践来提高受影响动物的性能,但使用发育不全的动物进行繁殖可能会导致这种疾病的流行率扩大。本研究的目的是通过全基因组关联研究(GWAS)和功能分析来确定与Nellore 牛的 TH 相关的基因组区域。本研究使用了来自 47563 头动物的表型和系谱数据以及来自 265 头公牛的基因型(500689 个单核苷酸多态性,SNP)。TH 作为 18 个月龄时测量的二元性状进行评估。使用贝叶斯方法拟合单性状阈值动物模型来计算估计育种值(EBV)。使用贝叶斯 C 方法估计 SNP 效应,并将 TH 的去回归 EBV 作为响应变量(拟表型)。确定了前 15 个排名窗口(5 个相邻 SNP),这些窗口解释了最高比例的方差,用于进一步的功能和生物网络分析。TH 的遗传力后验均值(95%最高后验密度)为 0.16(0.08;0.23)。最重要的基因组窗口位于 BTA1、BTA3、BTA4、BTA5、BTA9、BTA22、BTA23 和 BTA25。这些窗口共同解释了 TH 的总加性遗传方差的 22.69%。确定了与代谢和类固醇合成、细胞存活、精子发生过程和精子活力相关的重要候选基因,这些基因可能在 TH 的表达中发挥重要作用。我们的研究结果有助于更好地了解 TH,并对因果变异的未来表征可能会使牛肉牛中这种性状的基因组预测得到改善。