Codependent Activators Direct Myoblast-Specific MyoD Transcription

被引:130
作者
Hu, Ping [1 ]
Geles, Kenneth G. [1 ]
Paik, Ji-Hye [2 ,3 ]
DePinho, Ronald A. [2 ,3 ,4 ,5 ]
Tjian, Robert [1 ]
机构
[1] Univ Calif Berkeley, Howard Hughes Med Inst, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Harvard Univ, Sch Med, Inst Innovat Canc Sci, Dept Med Oncol,Dana Farber Canc Inst,Belfer Fdn, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Inst Innovat Canc Sci, Dept Med,Dana Farber Canc Inst,Belfer Fdn, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Inst Innovat Canc Sci, Dept Genet,Dana Farber Canc Inst,Belfer Fdn, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Ctr Appl Canc Sci,Inst Innovat Canc Sci, Dana Farber Canc Inst,Belfer Fdn, Boston, MA 02115 USA
关键词
D O I
10.1016/j.devcel.2008.08.018
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although FoxO and Pax proteins represent two important families of transcription factors in determining cell fate, they had not been functionally or physically linked together in mediating regulation of a common target gene during normal cellular transcription programs. Here, we identify MyoD, a key regulator of myogenesis, as a direct target of FoxO3 and Pax3/7 in myoblasts. Our cell-based assays and in vitro studies reveal a tight codependent partnership between FoxO3 and Pax3/7 to coordinately recruit RNA polymerase II and form a preinitiation complex (PIC) to activate MyoD transcription in myoblasts. The role of FoxO3 in regulating muscle differentiation is confirmed in vivo by observed defects in muscle regeneration caused by MyoD downregulation in FoxO3 null mice. These data establish a mutual interdependence and functional link between two families of transcription activators serving as potential signaling sensors and regulators of cell fate commitment in directing tissue specific MyoD transcription.
引用
收藏
页码:534 / 546
页数:13
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