Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Department of Cardiology, Yinzhou Hospital, Medical School of Ningbo University, Ningbo, China.
Biomed Res Int. 2018 May 30;2018:4658024. doi: 10.1155/2018/4658024. eCollection 2018.
In previous studies, we have demonstrated the function of uc.167 in the heart development. DNA methylation plays a crucial role in regulating the expression of developmental genes during embryonic development. In this study, the methylomic landscape was investigated in order to identify the DNA methylation alterations. Methylated DNA immunoprecipitation (MeDIP) was performed to examine the differences in methylation status of overexpressed uc.167 in P19 cells. GO and KEGG pathway analyses of differentially methylated genes were also conducted. We found that the distribution of differentially methylated regions (DMRs) peaks in different components of genome was mainly located in intergenic regions and intron. The biological process associated with uc.167 was focal adhesion and Rap1 signaling pathway. MEF2C was significantly decreased in uc.167 overexpressed group, suggesting that uc.167 may influence the P19 differentiation through MEF2C reduction. Taken together, our findings revealed that the effect of uc.167 on P19 differentiation may be attributed to the altered methylation of specific genes.
在之前的研究中,我们已经证明了 uc.167 在心脏发育中的功能。DNA 甲基化在胚胎发育过程中对调节发育基因的表达起着至关重要的作用。在这项研究中,我们调查了甲基组学图谱,以确定 DNA 甲基化的改变。采用甲基化 DNA 免疫沉淀(MeDIP)来检测过表达 uc.167 在 P19 细胞中的甲基化状态差异。还对差异甲基化基因进行了 GO 和 KEGG 通路分析。我们发现,差异甲基化区域(DMR)的分布在基因组的不同组成部分中呈峰状,主要位于基因间区和内含子。与 uc.167 相关的生物学过程是粘着斑和 Rap1 信号通路。uc.167 过表达组中 MEF2C 显著降低,提示 uc.167 可能通过降低 MEF2C 影响 P19 分化。总之,我们的研究结果表明,uc.167 对 P19 分化的影响可能归因于特定基因的甲基化改变。