Institute of Cell and Molecular Biology, Medical School, Wuhan University of Science and Technology, Wuhan, Hubei Province 430065, China.
FEBS Lett. 2011 Apr 6;585(7):1082-8. doi: 10.1016/j.febslet.2011.03.007. Epub 2011 Mar 6.
Human cytomegalovirus immediate early proteins (CMV IEs) are involved in transcriptional activities of both host and virus gene expression. This study shows that the transcriptional activity of myocardin in regulating cardiomyocyte hypertrophy is enhanced by co-expressing CMV IE2. Forced expression of IE2 increases the augmented cell size of neonatal rat cardiac myocytes induced by myocardin, as well as the mRNA and protein levels of hypertrophic genes, whereas deletion of CArG boxes in the atrial natriuretic factor (ANF) promoter attenuates the effect of CMV IE2 with myocardin. In conclusion, CMV IE2 synergistically stimulates myocardin transactivity in the hypertrophic marker gene ANF in a CArG box-dependent manner. Our study indicates that the association of CMV IEs with myocardin-induced transcription may be involved in myocardin-mediated cardiac hypertrophy.
人巨细胞病毒立即早期蛋白(CMV IEs)参与宿主和病毒基因表达的转录活性。本研究表明,CMV IE2 的共表达增强了 myocardin 调节心肌细胞肥大的转录活性。IE2 的强制表达增加了 myocardin 诱导的新生大鼠心肌细胞增大的细胞大小,以及肥大基因的 mRNA 和蛋白水平,而心房利钠肽(ANF)启动子中 CArG 盒的缺失则减弱了 CMV IE2 与 myocardin 的协同作用。总之,CMV IE2 以 CArG 盒依赖的方式协同刺激心肌细胞肥大标记基因 ANF 中的 myocardin 反式活性。我们的研究表明,CMV IEs 与 myocardin 诱导的转录的关联可能与 myocardin 介导的心脏肥大有关。