The RNA helicases p68/p72 and the noncoding RNA SRA are coregulators of MyoD and skeletal muscle differentiation

被引:254
作者
Caretti, Giuseppina
Schiltz, R. Louis
Dilworth, F. Jeffrey
Di Padova, Monica
Zhao, Po
Ogryzko, Vasily
Fuller-Pace, Frances V.
Hoffman, Eric P.
Tapscott, Stephen J.
Sartorelli, Vittorio [1 ]
机构
[1] NIAMSD, Muscle Gene Express Grp, Lab Muscle Biol, NIH, Bethesda, MD 20829 USA
[2] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[3] Ottawa Hlth Res Inst, Mol Med Program, Ottawa, ON K1H 8L6, Canada
[4] Res Ctr Genet Med, Washington, DC 20010 USA
[5] Childrens Natl Med Ctr, Washington, DC 20010 USA
[6] Inst Gustave Roussy, CNRS, UMR 8126, F-94100 Villejuif, France
[7] Univ Dundee, Ninewells Hosp & Med Sch, Canc Biol Grp, Div Pathol & Neurosci, Dundee DD1 9SY, Scotland
关键词
D O I
10.1016/j.devcel.2006.08.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MyoD regulates skeletal myogenesis. Since proteins associated with MyoD exert regulatory functions, their identification is expected to contribute important insights into the mechanisms governing gene expression in skeletal muscle. We have found that the RNA helicases p68/p72 are MyoD-associated proteins and that the noncoding RNA SRA also immunoprecipitates with MyoD. In vitro and in vivo experiments indicated that both p68/p72 and SRA are coactivators of MyoD. RNA interference toward either p68/p72 or SRA prevented proper activation of muscle gene expression and cell differentiation. Unexpectedly, reducing the levels of p68/p72 proteins impaired recruitment of the TATA binding protein TBP; RNA polymerase II; and the catalytic subunit of the ATPase SWI/SNF complex, Brg-1, and hindered chromatin remodeling. These findings reveal that p68/p72 play a critical role in promoting the assembly of proteins required for the formation of the transcription initiation complex and chromatin remodeling.
引用
收藏
页码:547 / 560
页数:14
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