Mariner Peter D, Luckey Stephen W, Long Carlin S, Sucharov Carmen C, Leinwand Leslie A
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Biochem Biophys Res Commun. 2005 Jan 7;326(1):79-86. doi: 10.1016/j.bbrc.2004.11.008.
In the work presented here, we elucidate a mechanism for the repression of alpha-myosin heavy chain (MyHC) during pathological cardiac hypertrophy. We demonstrate that the transcription factor Yin Yang 1 (YY1) significantly decreases endogenous alpha-MyHC mRNA and protein expression in neonatal rat ventricular myocytes. Furthermore, mutation of the YY1 binding sites in the proximal rat alpha-MyHC promoter increases promoter activity and alleviates YY1-mediated repression of the promoter. Despite the presence of 5 sites that bind YY1, only one site, located at -94bp of the rat alpha-MyHC promoter, is both necessary and sufficient for pathological repression of the promoter by phorbol esters, revealing a unique mechanism for the repression of alpha-MyHC expression during cardiac hypertrophy.
在本文展示的研究工作中,我们阐明了病理性心肌肥大过程中α-肌球蛋白重链(MyHC)受到抑制的机制。我们证明转录因子阴阳1(YY1)可显著降低新生大鼠心室肌细胞中内源性α-MyHC mRNA和蛋白质的表达。此外,大鼠α-MyHC近端启动子中YY1结合位点的突变可增强启动子活性,并减轻YY1介导的启动子抑制作用。尽管存在5个可结合YY1的位点,但只有位于大鼠α-MyHC启动子-94bp处的一个位点对于佛波酯对启动子的病理性抑制是必需且充分的,这揭示了心肌肥大过程中α-MyHC表达受到抑制的独特机制。