MyoD公司
肌发生
皮特x2
肌生成素
肌动蛋白
生物
细胞生物学
C2C12型
肌源性调节因子
细胞分化
心肌细胞
细胞生长
转录因子
遗传学
基因
同源盒
作者
Xun Jin,Jong-Gun Kim,Myung‐Joo Oh,Ho-Yeon Oh,Young-Woo Sohn,Xumin Pian,Jinlong Yin,Samuel J. Beck,Nam-Kyung Lee,Jee Soo Son,Hyunggee Kim,Chang−Guo Yan,Ji Hui Wang,Yun-Jaie Choi,Kwang Youn Whang
标识
DOI:10.1016/j.bbrc.2007.10.042
摘要
The basic helix-loop-helix myogenic regulatory factors play critical roles in skeletal myogenesis. Among the myogenic regulatory factors (MRFs), MRF4 shows a biphasic expression pattern during the formation of myotomes, although its function remains unclear. In this study, we used BEF (spontaneously immortalized bovine embryonic fibroblast that shows myogenic differentiation by overexpression of MyoD) and C2C12 cells to investigate the function of MRF4. Ectopic expressions of MRF4 did not stimulate myogenic differentiation in the BEF and C2C12 cells, but did show a marked increase of cell proliferation, upregulation of cyclin E, and downregulation of p21WAF1. Furthermore, MRF4 was found to induce degradation of the MyoD protein, which acts as a transcriptional activator for p21WAF1, and thus indicates that MRF4 accelerates cell proliferation by suppressing MyoD-dependent p21WAF1 expression. However, forced expression of MyoD in the MRF4-overexpressing cells inhibited cell proliferation and partially induced myogenic differentiation, which suggests that MyoD is a potential negative intercessor of MRF4 in the regulation of the cell cycle. Taken together, these results indicate that MRF4 and MyoD play competitive roles in myogenesis by stimulating cell proliferation and differentiation, respectively.
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