| Literature DB >> 29754779 |
Xudong Guo1, Yanxin Xu2, Zikang Wang2, Yukang Wu2, Jiayu Chen3, Guiying Wang2, Chenqi Lu4, Wenwen Jia2, Jiajie Xi2, Songcheng Zhu2, Zeyidan Jiapaer2, Xiaoping Wan5, Zhongmin Liu6, Shaorong Gao3, Jiuhong Kang7.
Abstract
Large intergenic non-coding RNAs (lincRNAs) play widespread roles in epigenetic regulation during multiple differentiation processes, but little is known about their mode of action in cardiac differentiation. Here, we identified the key roles of a lincRNA, termed linc1405, in modulating the core network of cardiac differentiation by functionally interacting with Eomes. Chromatin- and RNA-immunoprecipitation assays showed that exon 2 of linc1405 physically mediates a complex consisting of Eomes, trithorax group (TrxG) subunit WDR5, and histone acetyltransferase GCN5 binding at the enhancer region of Mesp1 gene and activates its expression during cardiac mesoderm specification of embryonic stem cells. Importantly, linc1405 co-localizes with Eomes, WDR5, and GCN5 at the primitive streak, and linc1405 depletion impairs heart development and function in vivo. In summary, linc1405 mediates a Eomes/WDR5/GCN5 complex that contributes to cardiogenesis, highlighting the critical roles of lincRNA-based complexes in the epigenetic regulation of cardiogenesis in vitro and in vivo.Entities:
Keywords: Eomes; cardiac differentiation; enhancer; epigenetic regulation; lincRNA
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Year: 2018 PMID: 29754779 DOI: 10.1016/j.stem.2018.04.013
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633