Wang Yanru, Zheng Yuanyuan, Guo Dan, Zhang Xinghui, Guo Suling, Hui Taiyu, Yue Chang, Sun Jiaming, Guo Suping, Bai Zhixian, Cai Weidong, Zhang Xinjiang, Fan Yixing, Wang Zeying, Bai Wenlin
College of Animal Science & Veterinary Medicine, Shenyang Agricultural University, Shenyang, China.
Academy of Animal Husbandry Science of Liaoning Province, Liaoyang, China.
Front Genet. 2020 Jan 22;10:1318. doi: 10.3389/fgene.2019.01318. eCollection 2019.
N6-methyladenosine (m6A) is the most common internal modification in mRNAs of all higher eukaryotes. Here we perform two high-throughput sequencing methods, m6A-modified RNA immunoprecipitation sequence (MeRIP-seq) and RNA sequence (RNA-seq) to identify key genes with m6A modification in cashmere fiber growth. A total of 9,085 m6A sites were differentially RNA m6A methylated as reported from by MeRIP-seq, including 7,170 upregulated and 1,915 downregulated. In addition, by comparing m6A-modified genes between the fine-type Liaoning cashmere goat (FT-LCG) and coarse-type Liaoning Cashmere Goat (CT-LCG) skin samples, we obtain 1,170 differentially expressed genes. In order to identify the differently methylated genes related to cashmere fiber growth, 19 genes were selected to validate by performing qRT-PCR in FT-LCG and CT-LCG. In addition, GO enrichment analysis shows that differently methylated genes are mainly involved in keratin filament and intermediate filament. These findings provide a theoretical basis for future research on the function of m6A modification during the growth of cashmere fiber.
N6-甲基腺苷(m6A)是所有高等真核生物mRNA中最常见的内部修饰。在此,我们采用两种高通量测序方法,即m6A修饰的RNA免疫沉淀测序(MeRIP-seq)和RNA测序(RNA-seq),以鉴定在羊绒纤维生长过程中发生m6A修饰的关键基因。MeRIP-seq报告称,共有9085个m6A位点存在差异RNA m6A甲基化,其中7170个上调,1915个下调。此外,通过比较细型辽宁绒山羊(FT-LCG)和粗型辽宁绒山羊(CT-LCG)皮肤样本之间的m6A修饰基因,我们获得了1170个差异表达基因。为了鉴定与羊绒纤维生长相关的差异甲基化基因,选择了19个基因在FT-LCG和CT-LCG中进行qRT-PCR验证。此外,GO富集分析表明,差异甲基化基因主要参与角蛋白丝和中间丝。这些发现为未来研究m6A修饰在羊绒纤维生长过程中的功能提供了理论基础。