Department of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA.
Animal Genomics and Improvement Laboratory, Henry A. Wallace Beltsville Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
BMC Genomics. 2020 Jan 13;21(1):41. doi: 10.1186/s12864-020-6461-z.
Health traits are of significant economic importance to the dairy industry due to their effects on milk production and associated treatment costs. Genome-wide association studies (GWAS) provide a means to identify associated genomic variants and thus reveal insights into the genetic architecture of complex traits and diseases. The objective of this study is to investigate the genetic basis of seven health traits in dairy cattle and to identify potential candidate genes associated with cattle health using GWAS, fine mapping, and analyses of multi-tissue transcriptome data.
We studied cow livability and six direct disease traits, mastitis, ketosis, hypocalcemia, displaced abomasum, metritis, and retained placenta, using de-regressed breeding values and more than three million imputed DNA sequence variants. After data edits and filtering on reliability, the number of bulls included in the analyses ranged from 11,880 (hypocalcemia) to 24,699 (livability). GWAS was performed using a mixed-model association test, and a Bayesian fine-mapping procedure was conducted to calculate a posterior probability of causality to each variant and gene in the candidate regions. The GWAS detected a total of eight genome-wide significant associations for three traits, cow livability, ketosis, and hypocalcemia, including the bovine Major Histocompatibility Complex (MHC) region associated with livability. Our fine-mapping of associated regions reported 20 candidate genes with the highest posterior probabilities of causality for cattle health. Combined with transcriptome data across multiple tissues in cattle, we further exploited these candidate genes to identify specific expression patterns in disease-related tissues and relevant biological explanations such as the expression of Group-specific Component (GC) in the liver and association with mastitis as well as the Coiled-Coil Domain Containing 88C (CCDC88C) expression in CD8 cells and association with cow livability.
Collectively, our analyses report six significant associations and 20 candidate genes of cattle health. With the integration of multi-tissue transcriptome data, our results provide useful information for future functional studies and better understanding of the biological relationship between genetics and disease susceptibility in cattle.
健康特征对乳制品行业具有重要的经济意义,因为它们会影响牛奶产量和相关的治疗成本。全基因组关联研究(GWAS)提供了一种识别相关基因组变异的方法,从而揭示了复杂特征和疾病的遗传结构的见解。本研究的目的是研究奶牛的 7 种健康特征的遗传基础,并使用 GWAS、精细映射和多组织转录组数据分析来鉴定与牛健康相关的潜在候选基因。
我们使用去回归的繁殖值和超过三百万个导入的 DNA 序列变异来研究奶牛的生存能力和六种直接疾病特征,包括乳腺炎、酮病、低血钙症、皱胃移位、子宫炎和胎衣不下。在对可靠性进行数据编辑和过滤后,分析中包括的公牛数量从 11880 头(低血钙症)到 24699 头(生存能力)不等。使用混合模型关联测试进行 GWAS,并进行贝叶斯精细映射程序,以计算候选区域中每个变体和基因的因果关系后验概率。GWAS 总共检测到三个特征(奶牛生存能力、酮病和低血钙症)的 8 个全基因组显著关联,包括与生存能力相关的牛主要组织相容性复合体(MHC)区域。我们对相关区域的精细映射报告了 20 个候选基因,这些基因具有与牛健康的最高因果关系后验概率。结合牛的多个组织的转录组数据,我们进一步利用这些候选基因在疾病相关组织中识别特定的表达模式,并提供相关的生物学解释,例如肝脏中的 Group-specific Component (GC) 表达与乳腺炎的关联,以及 CD8 细胞中的 Coiled-Coil Domain Containing 88C (CCDC88C) 表达与奶牛生存能力的关联。
总的来说,我们的分析报告了 6 个与牛健康相关的显著关联和 20 个候选基因。通过整合多组织转录组数据,我们的结果为未来的功能研究提供了有用的信息,并更好地理解了遗传与牛疾病易感性之间的生物学关系。