Dairy Cattle Research Center, Shandong Academy of Agricultural Sciences, Jinan, Shandong, 250131, People's Republic of China.
Engineering Center of Animal Breeding and Reproduction, Jinan, Shandong, 250100, People's Republic of China.
BMC Genomics. 2020 Jan 30;21(1):102. doi: 10.1186/s12864-020-6526-z.
Neutrophils are the first effectors of inflammatory response triggered by mastitis infection, and are important defense cells against pathogenic Escherichia coli (E. coli). DNA methylation, as a critical epigenetic mechanism for regulating gene function, is involved in bovine mastitis.
In this study, we sequenced the blood neutrophils of healthy and E. coli-infected mastitic half-sib cows for the overall DNA methylation levels using transcriptome sequencing and reduced representation bisulfite sequencing. The methylation levels in the mastitis cows (MCs) were decreased compared with healthy cows (HCs). A total of 494 differentially methylated regions were identified, among which 61 were up-methylated and 433 were down-methylated (MCs vs. HCs). The expression levels of 1094 differentially expressed genes were up-regulated, and 245 genes were down-regulated. Twenty-nine genes were found in methylation and transcription data, among which seven genes' promoter methylation levels were negatively correlated with expression levels, and 11 genes were differentially methylated in the exon regions. The bisulfite sequencing PCR and quantitative real-time PCR validation results demonstrated that the promoter methylation of CITED2 and SLC40A1 genes affected differential expression. The methylation of LGR4 exon 5 regulated its own alternative splicing. The promoter methylation of bta-miR-15a has an indirect effect on the expression of its target gene CD163. The CITED2, SLC40A1, and LGR4 genes can be used as candidates for E. coli-induced mastitis resistance.
This study explored the roles of DNA methylation in affecting transcription of protein-coding genes and miRNAs in E. coli-induced mastitis, thereby helping explain the function of DNA methylation in the pathogenesis of mastitis and provided new target genes and epigenetic markers for mastitis resistance breeding in dairy cattle.
中性粒细胞是由乳腺炎感染引发的炎症反应的第一效应细胞,也是对抗致病性大肠杆菌(E. coli)的重要防御细胞。DNA 甲基化作为调控基因功能的关键表观遗传机制,参与了奶牛乳腺炎。
本研究采用转录组测序和简化重亚硫酸盐测序对健康和大肠杆菌感染乳腺炎半同胞奶牛的血液中性粒细胞进行了全基因组 DNA 甲基化水平测序。乳腺炎奶牛(MCs)的甲基化水平较健康奶牛(HCs)降低。共鉴定出 494 个差异甲基化区域,其中 61 个呈高甲基化,433 个呈低甲基化(MCs 与 HCs 相比)。1094 个差异表达基因的表达水平上调,245 个基因下调。在甲基化和转录数据中发现了 29 个基因,其中 7 个基因启动子的甲基化水平与表达水平呈负相关,11 个基因在外显子区域存在差异甲基化。亚硫酸氢盐测序 PCR 和定量实时 PCR 验证结果表明,CITED2 和 SLC40A1 基因启动子的甲基化影响了差异表达。LGR4 外显子 5 的甲基化调控了自身的选择性剪接。bta-miR-15a 的启动子甲基化对其靶基因 CD163 的表达有间接影响。CITED2、SLC40A1 和 LGR4 基因可作为大肠杆菌诱导乳腺炎抗性的候选基因。
本研究探讨了 DNA 甲基化在影响大肠杆菌诱导乳腺炎中蛋白编码基因和 miRNA 转录的作用,从而有助于解释 DNA 甲基化在乳腺炎发病机制中的功能,并为奶牛乳腺炎抗性育种提供了新的靶基因和表观遗传标记。