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RNA-binding motif protein 24 regulates myogenin expression and promotes myogenic differentiation
被引:50
作者:
Jin, Donghao
[1
]
Hidaka, Kyoko
[1
]
Shirai, Manabu
[1
]
Morisaki, Takayuki
[1
,2
]
机构:
[1] Natl Cardiovasc Ctr, Res Inst, Dept Biosci, Osaka 5658565, Japan
[2] Osaka Univ, Grad Sch Pharmaceut Sci, Dept Mol Pathophysiol, Osaka 5658565, Japan
关键词:
MYOD MESSENGER-RNA;
MUSCLE DIFFERENTIATION;
HUR;
STABILITY;
DECAY;
STABILIZATION;
TRANSLATION;
INHIBITION;
COMPLEXES;
PATHWAYS;
D O I:
10.1111/j.1365-2443.2010.01446.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The formation of muscle fibers involves sequential expression of many proteins that regulate key steps during myoblast-to-myotube transition. Myogenin is a major player in the initiation and maintenance of myogenic differentiation in a mouse myoblast cell line, C2C12. RNA-binding proteins bind to specific target RNA sequences and regulate gene expression in a post-transcriptional manner. This study demonstrates that RNA-binding motif protein 24 (Rbm24) interacts with the 3'-untranslated region of myogenin mRNA and affects its half-life in C2C12 myogenesis. Knockdown of Rbm24 expression by RNA interference significantly decreased myogenin expression associated with the inhibition of myogenesis. In contrast, the overexpression of Rbm24 by stable transfection of a plasmid increased myogenin expression and had a positive effect on myogenic differentiation. Ectopic expression of myogenin was also able to restore myogenic differentiation in Rbm24-knockdown cells. Together, our results suggest that Rbm24 binds to myogenin mRNA and regulates its stability in C2C12 cells. Rbm24 plays a crucial role in myogenic differentiation at least in part through a myogenin-dependent post-transcriptional regulatory pathway.
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页码:1158 / 1167
页数:10
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