Institute of Biology and Medicine, Wuhan University of Science and Technology, Wuhan 430065, China.
Institute of Biology and Medicine, Wuhan University of Science and Technology, Wuhan 430065, China.
Cell Signal. 2018 Mar;43:11-20. doi: 10.1016/j.cellsig.2017.11.007. Epub 2017 Dec 5.
As a strong transactivator of promoters containing CarG boxes, myocardin was critical for the cardiac muscle program and necessary for normal cardiogenesis. So it probably represents a viable therapeutic biomarker in the setting of cardiac hypertrophy and failure. In recent years, the studies of regulation of cardiac hypertrophy via myocardin are so common, and the molecular mechanism is becoming more and more clear. Here, we have revealed a kind of interaction between mhrt and myocardin shown as a feedback regulatory mechanism in the regulation of cardiac hypertrophy. That is, the lncRNA mhrt can affect the acetylation of myocardin by HDAC5 to inhibit cardiac hypertrophy induced by myocardin. Moreover, myocardin also can directly activate the mhrt transcription through binding to the CarG box. Thus, mhrt and myocardin form a regulation loop in the process of cardiac hypertrophy. This finding may play a positive role in revealing the complete mechanisms of cardiac hypertrophy.
作为含有 CarG 盒的启动子的强转录激活子,myocardin 对于心肌程序至关重要,也是正常心肌发生所必需的。因此,它可能代表了心脏肥大和衰竭情况下有前途的治疗生物标志物。近年来,通过 myocardin 调节心脏肥大的研究非常普遍,分子机制也越来越清楚。在这里,我们揭示了一种 mhrt 和 myocardin 之间的相互作用,这种相互作用表现为一种反馈调节机制,调节心脏肥大。也就是说,lncRNA mhrt 可以通过 HDAC5 影响 myocardin 的乙酰化,从而抑制 myocardin 诱导的心脏肥大。此外,myocardin 还可以通过与 CarG 盒结合直接激活 mhrt 的转录。因此,mhrt 和 myocardin 在心脏肥大过程中形成一个调节环路。这一发现可能对揭示心脏肥大的完整机制起到积极作用。