National Engineering Laboratory for Animal Breeding, Key Laboratory of Animal Genetics, Breeding and Reproduction of Ministry of Agriculture and Rural Affairs, College of Animal Science and Technology, China Agricultural University, Beijing, 100193, China.
College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450002, China.
BMC Genomics. 2020 Jul 17;21(1):489. doi: 10.1186/s12864-020-06909-z.
Ketosis is a common metabolic disease during the transition period in dairy cattle, resulting in long-term economic loss to the dairy industry worldwide. While genetic selection of resistance to ketosis has been adopted by many countries, the genetic and biological basis underlying ketosis is poorly understood.
We collected a total of 24 blood samples from 12 Holstein cows, including 4 healthy and 8 ketosis-diagnosed ones, before (2 weeks) and after (5 days) calving, respectively. We then generated RNA-Sequencing (RNA-Seq) data and seven blood biochemical indicators (bio-indicators) from leukocytes and plasma in each of these samples, respectively. By employing a weighted gene co-expression network analysis (WGCNA), we detected that 4 out of 16 gene-modules, which were significantly engaged in lipid metabolism and immune responses, were transcriptionally (FDR < 0.05) correlated with postpartum ketosis and several bio-indicators (e.g., high-density lipoprotein and low-density lipoprotein). By conducting genome-wide association signal (GWAS) enrichment analysis among six common health traits (ketosis, mastitis, displaced abomasum, metritis, hypocalcemia and livability), we found that 4 out of 16 modules were genetically (FDR < 0.05) associated with ketosis, among which three were correlated with postpartum ketosis based on WGCNA. We further identified five candidate genes for ketosis, including GRINA, MAF1, MAFA, C14H8orf82 and RECQL4. Our phenome-wide association analysis (Phe-WAS) demonstrated that human orthologues of these candidate genes were also significantly associated with many metabolic, endocrine, and immune traits in humans. For instance, MAFA, which is involved in insulin secretion, glucose response, and transcriptional regulation, showed a significantly higher association with metabolic and endocrine traits compared to other types of traits in humans.
In summary, our study provides novel insights into the molecular mechanism underlying ketosis in cattle, and highlights that an integrative analysis of omics data and cross-species mapping are promising for illustrating the genetic architecture underpinning complex traits.
酮病是奶牛过渡期的一种常见代谢疾病,给全球的奶牛业带来了长期的经济损失。虽然许多国家已经采用了对酮病的抗性遗传选择,但酮病的遗传和生物学基础还知之甚少。
我们共采集了 12 头荷斯坦奶牛的 24 份血样,其中 4 份为健康牛,8 份为酮病牛,分别在产后 2 周和产后 5 天采集。我们分别从白细胞和血浆中生成了这些样本的 RNA 测序(RNA-Seq)数据和 7 个血液生化指标(生物指标)。通过使用加权基因共表达网络分析(WGCNA),我们检测到 16 个基因模块中的 4 个,这些模块主要参与脂代谢和免疫反应,与产后酮病和几种生物指标(如高密度脂蛋白和低密度脂蛋白)转录相关(FDR<0.05)。通过对 6 种常见健康性状(酮病、乳腺炎、瘤胃移位、子宫炎、低血钙和成活率)的全基因组关联信号(GWAS)富集分析,我们发现 16 个模块中的 4 个与酮病在遗传上(FDR<0.05)相关,其中 3 个与 WGCNA 基于产后酮病相关。我们进一步确定了 5 个与酮病相关的候选基因,包括 GRINA、MAF1、MAFA、C14H8orf82 和 RECQL4。我们的表型全基因组关联分析(Phe-WAS)表明,这些候选基因的人类同源物也与人类的许多代谢、内分泌和免疫性状显著相关。例如,参与胰岛素分泌、葡萄糖反应和转录调控的 MAFA 与代谢和内分泌性状的关联明显高于其他类型的性状。
总之,我们的研究为牛酮病的分子机制提供了新的见解,并强调了组学数据的综合分析和跨物种映射对于阐明复杂性状的遗传结构是很有前景的。