Department of Biology, Wakayama Medical University, Japan.
Department of Ophthalmology, Yamaguchi University Graduate School of Medicine, Japan.
FEBS Open Bio. 2023 Feb;13(2):363-379. doi: 10.1002/2211-5463.13549. Epub 2023 Jan 12.
MYOCD is a transcription factor important for cardiac and smooth muscle development. We previously identified that actin-related protein 5 (ARP5) binds to the N-terminus of MYOCD. Here, we demonstrate that ARP5 inhibits the cooperative action of the cardiac-specific isoform of MYOCD with MEF2. ARP5 overexpression in murine hearts induced cardiac hypertrophy and fibrosis, whereas ARP5 knockdown in P19CL6 cells significantly increased cardiac gene expression. ARP5 was found to bind to a MEF2-binding motif of cardiac MYOCD and inhibit MEF2-mediated transactivation by MYOCD. RNA-seq analysis revealed 849 genes that are upregulated by MYOCD-MEF2 and 650 genes that are repressed by ARP5. ARP5 expression increased with cardiomyopathy and was negatively correlated with the expression of Tnnt2 and Ttn, which were regulated by cardiac MYOCD-MEF2. Overall, our data suggest that ARP5 is a potential suppressor of cardiac MYOCD during physiological and pathological processes.
肌球蛋白结合蛋白 C 相关蛋白激酶(MYOCD)是一种在心脏和平滑肌发育中起重要作用的转录因子。我们之前发现肌动蛋白相关蛋白 5(ARP5)与 MYOCD 的 N 端结合。在这里,我们证明 ARP5 抑制了心脏特异性同工型 MYOCD 与 MEF2 的协同作用。ARP5 在鼠心中的过表达诱导了心脏肥大和纤维化,而 P19CL6 细胞中的 ARP5 敲低则显著增加了心脏基因的表达。发现 ARP5 与心脏 MYOCD 的 MEF2 结合基序结合,并抑制 MYOCD 介导的 MEF2 转录激活。RNA-seq 分析显示,有 849 个基因被 MYOCD-MEF2 上调,650 个基因被 ARP5 下调。ARP5 的表达随着心肌病而增加,与 Tnnt2 和 Ttn 的表达呈负相关,而 Tnnt2 和 Ttn 是由心脏 MYOCD-MEF2 调节的。总的来说,我们的数据表明,ARP5 是生理和病理过程中心脏 MYOCD 的潜在抑制因子。