Han Bingshe, Li Wenhao, Chen Zuozhou, Xu Qiongqiong, Luo Juntao, Shi Yingdi, Li Xiaoxia, Yan Xiaonan, Zhang Junfang
Key Laboratory of Aquacultural Resources and Utilization, Ministry of Education, College of Fishery and Life Science, Shanghai Ocean University, Shanghai, China.
PLoS One. 2016 Aug 5;11(8):e0160358. doi: 10.1371/journal.pone.0160358. eCollection 2016.
DNA methylation is an essential epigenetic mechanism involved in multiple biological processes. However, the relationship between DNA methylation and cold acclimation remains poorly understood. In this study, Methylated DNA Immunoprecipitation Sequencing (MeDIP-seq) was performed to reveal a genome-wide methylation profile of zebrafish (Danio rerio) embryonic fibroblast cells (ZF4) and its variation under cold pressure. MeDIP-seq assay was conducted with ZF4 cells cultured at appropriate temperature of 28°C and at low temperature of 18°C for 5 (short-term) and 30 (long-term) days, respectively. Our data showed that DNA methylation level of whole genome increased after a short-term cold exposure and decreased after a long-term cold exposure. It is interesting that metabolism of folate pathway is significantly hypomethylated after short-term cold exposure, which is consistent with the increased DNA methylation level. 21% of methylation peaks were significantly altered after cold treatment. About 8% of altered DNA methylation peaks are located in promoter regions, while the majority of them are located in non-coding regions. Methylation of genes involved in multiple cold responsive biological processes were significantly affected, such as anti-oxidant system, apoptosis, development, chromatin modifying and immune system suggesting that those processes are responsive to cold stress through regulation of DNA methylation. Our data indicate the involvement of DNA methylation in cellular response to cold pressure, and put a new insight into the genome-wide epigenetic regulation under cold pressure.
DNA甲基化是一种参与多种生物学过程的重要表观遗传机制。然而,DNA甲基化与冷驯化之间的关系仍知之甚少。在本研究中,进行了甲基化DNA免疫沉淀测序(MeDIP-seq),以揭示斑马鱼(Danio rerio)胚胎成纤维细胞(ZF4)的全基因组甲基化图谱及其在冷胁迫下的变化。MeDIP-seq分析分别在28°C适宜温度和18°C低温下培养5天(短期)和30天(长期)的ZF4细胞中进行。我们的数据表明,短期冷暴露后全基因组的DNA甲基化水平升高,长期冷暴露后降低。有趣的是,短期冷暴露后叶酸途径的代谢显著低甲基化,这与DNA甲基化水平的升高一致。冷处理后21%的甲基化峰发生了显著改变。约8%的改变的DNA甲基化峰位于启动子区域,而其中大多数位于非编码区域。参与多种冷响应生物学过程的基因甲基化受到显著影响,如抗氧化系统、细胞凋亡、发育、染色质修饰和免疫系统,这表明这些过程通过DNA甲基化的调节对冷胁迫作出反应。我们的数据表明DNA甲基化参与细胞对冷胁迫的反应,并为冷胁迫下的全基因组表观遗传调控提供了新的见解。