Department of Pediatrics, Darby Children's Research Institute and Shawn Jenkins Children's Hospital, Medical University of South Carolina, Charleston, SC, United States of America.
Department of Pediatrics, Darby Children's Research Institute and Shawn Jenkins Children's Hospital, Medical University of South Carolina, Charleston, SC, United States of America; Regenerative Medicine and Cell Biology Department, Medical University of South Carolina, Charleston, SC, United States of America.
Mech Dev. 2020 Jun;162:103615. doi: 10.1016/j.mod.2020.103615. Epub 2020 May 22.
The cardiac homeobox transcription factor Nkx2-5 is a major determinant of cardiac identity and cardiac morphogenesis. Nkx2-5 operates as part of a complex and mutually reinforcing network of early transcription factors of the homeobox, GATA zinc finger and MADS domain families to initiate the program of cardiac development and differentiation, particularly in outflow tract precursor cells in the second heart field (SHF). We have now found evidence for another aspect of cardiac transcription factor cooperativity between Nkx2-5 and the cardiac enriched MADS domain transcription factor Srf. Specifically, Srf interaction with an evolutionarily conserved binding site in the Nkx2-5 CpG island-like proximal promoter is required for cardiac specific expression mediated by an SHF enhancer, and for combinatorial activation of these elements by cardiac transcription factors. These results provide further insight into cooperative gene regulation during cardiogenesis at the level of promoter-enhancer interactions.
心脏同源盒转录因子 Nkx2-5 是心脏特征和心脏形态发生的主要决定因素。Nkx2-5 作为同源盒、GATA 锌指和 MADS 结构域家族的早期转录因子的复杂且相互增强的网络的一部分发挥作用,以启动心脏发育和分化的程序,特别是在第二心区(SHF)的流出道前体细胞中。我们现在已经发现了 Nkx2-5 和心脏富集的 MADS 结构域转录因子 Srf 之间心脏转录因子协同作用的另一个方面的证据。具体而言,Srf 与 Nkx2-5 CpG 岛样近端启动子中的进化上保守的结合位点相互作用,对于由 SHF 增强子介导的心脏特异性表达以及心脏转录因子对这些元件的组合激活是必需的。这些结果提供了在心脏发生过程中启动子-增强子相互作用水平上的协同基因调控的进一步见解。