五年期
MyoD公司
肌生成素
肌发生
生物
C2C12型
肌源性调节因子
心肌细胞
细胞融合
细胞生物学
肌动蛋白
骨骼肌
融合蛋白
分子生物学
遗传学
细胞
内分泌学
基因
重组DNA
作者
Stéphane Dedieu,Germain Mazères,Patrick Cottin,Jean‐Jacques Brustis
出处
期刊:PubMed
日期:2002-03-01
卷期号:46 (2): 235-41
被引量:129
摘要
The myogenic factors, MyoD, myogenin, Myf5 and MRF4, can activate skeletal muscle differentiation when overexpressed in non-muscular cells. Gene targeting experiments have provided much insight into the in vivo functions of MRF and have defined two functional groups of MRFs. MyoD and Myf5 may be necessary for myoblast determination while myogenin and MRF4 may be required later during differentiation. However, the specific role of these myogenic factors has not been clearly defined during one important stage of myogenesis: the fusion of myoblasts. Using cultured C2C12 mouse muscular cells, the time-course of these proteins was analyzed and a distinct expression pattern in fusing cells was revealed. In an attempt to clarify the role of each of these regulators during myoblast fusion, an antisense strategy using oligonucleotides with phosphorothioate backbone modification was adoped. The results showed that the inhibition of myogenin and Myf5 activity is capable of significantly preventing fusion. Furthermore, the inhibition of MyoD can wholly arrest the engaged fusion process in spite of high endogenous expression of both myogenin and Myf5. Consequently, each MRF seems to have, at this defined step of myogenesis, a specific set of functions that can not be substituted for by the others and therefore may regulate a distinct subset of muscle-specific genes at the onset of fusion.
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