Liu Hui, Ma Yingying, Yu Jiaxin, Chen Xiang, Wang Shuyuan, Jia Yijie, Ding Na, Jin Xiaoyan, Zhang Yunpeng, Xu Juan, Li Xia
College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang 150081, China.
Mol Ther Nucleic Acids. 2023 Aug 1;33:629-641. doi: 10.1016/j.omtn.2023.07.033. eCollection 2023 Sep 12.
Cardiogenesis is an extremely complicated process involved with DNA regulatory elements, and factors regulate gene expression pattern spatiotemporally. Enhancers, as the well-known DNA elements, activate target gene expression by transcription factors (TFs) occupied to organize dynamic three-dimensional (3D) interactions, which when affected or interrupted might cause heart defects or diseases. In this study, we integrated transcriptome, 3D genome, and regulatome to reorganize the global 3D genome in cardiomyogenesis, showing a gradually decreased trend of both chromatin interactions and topological associating domains (TADs) during cardiomyocyte differentiation. And almost all of the chromatin interactions occurred within the same or between adjacent TADs involved with enhancers, indicating that dynamical rewiring of enhancer-related chromatin interactions in the continuous expansive TADs is closely correlated to cardiogenesis. Moreover, we found stage-specific interactions activate stage-specific expression to be involved within corresponding biological functions, and the stage-specific combined regulations of enhancers and binding TFs form connected networks to control stage-specific expression and biological processes, which promote cardiomyocyte differentiation. Finally, we identified markers based on regulatory networks, which might drive cardiac development. This study demonstrates the power of enhancer interactome combined with active TFs to reveal insights into transcriptional regulatory networks during cardiomyogenesis.
心脏发生是一个极其复杂的过程,涉及DNA调控元件,且多种因子在时空上调节基因表达模式。增强子作为著名的DNA元件,通过转录因子(TFs)占据来激活靶基因表达,从而组织动态三维(3D)相互作用,这种相互作用若受到影响或中断可能会导致心脏缺陷或疾病。在本研究中,我们整合了转录组、3D基因组和调控组,以重组心肌发生过程中的全局3D基因组,结果显示在心肌细胞分化过程中,染色质相互作用和拓扑相关结构域(TADs)均呈逐渐下降趋势。并且几乎所有的染色质相互作用都发生在与增强子相关的同一TAD内或相邻TAD之间,这表明在不断扩展的TAD中,与增强子相关的染色质相互作用的动态重塑与心脏发生密切相关。此外,我们发现阶段特异性相互作用激活阶段特异性表达并参与相应的生物学功能,增强子与结合TFs的阶段特异性联合调控形成连接网络,以控制阶段特异性表达和生物学过程,从而促进心肌细胞分化。最后,我们基于调控网络鉴定出可能驱动心脏发育的标志物。本研究证明了增强子相互作用组与活性TFs相结合在揭示心肌发生过程中转录调控网络方面的强大作用。