MRF4 can substitute for myogenin during early stages of myogenesis

被引:0
|
作者
Zhu, ZM
Miller, JB
机构
[1] MASSACHUSETTS GEN HOSP,NEUROMUSCULAR LAB,CHARLESTOWN,MA 02129
[2] HARVARD UNIV,SCH MED,PROGRAM NEUROSCI,BOSTON,MA 02115
关键词
MRF4; myogenin; myogenesis; regulatory loops; transgenic mouse;
D O I
10.1002/(SICI)1097-0177(199706)209:2<233::AID-AJA9>3.0.CO;2-J
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
MRF4, myogenin, MyoD, and Myf-5 are the four members of the basic helix-loop-helix family of muscle-specific regulatory factors (MRFs), We examined whether MRF4 could substitute for myogenin in vivo by determining if the myofiber- and MRF4-deficient phenotype of myogenin (-/-) mice could be rescued by a myogenin promoter-MRF4 transgene. When the transgene was expressed at a physiological level in myogenin-deficient fetuses, we found that expression of the endogenous MRF4 gene was restored to normal levels, whereas MyoD levels were unchanged. Thus, MRF4 can participate in a positive autoregulatory loop and can substitute for myogenin to activate its own promoter. Myogenin-deficient fetuses that expressed the transgene also had more myosin, more and larger myofibers, and a more normal ribcage morphology than myogenin-deficient littermates without the transgene, The transgene failed, however, to restore normal numbers of myofibers or viability to myogenin-deficient mice, because the similar to 1.6 kb myogenin promoter fragment was not expressed in most late-forming myofibers. These results demonstrate that MRF4 is able to substitute for myogenin to activate MRF4 expression and promote myofiber formation during the early stages of myogenesis. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:233 / 241
页数:9
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