MyoD Targets TAF3/TRF3 to Activate Myogenin Transcription

被引:123
作者
Deato, Maria Divina E. [1 ]
Marr, Michael T. [3 ]
Sottero, Theo [1 ]
Inouye, Carla [1 ]
Hu, Ping [1 ]
Tjian, Robert [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Li Ka Shing Ctr Biomed & Hlth Sci, Berkeley, CA 94720 USA
[3] Brandeis Univ, Dept Biol MS 029, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USA
关键词
D O I
10.1016/j.molcel.2008.09.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Skeletal muscle differentiation requires a cascade of transcriptional events to control the spatial and temporal expression of muscle-specific genes. Until recently, muscle-specific transcription was primarily attributed to prototypic enhancer-binding factors, while the role of core promoter recognition complexes in directing myogenesis remained unknown. Here, we report the development of a purified reconstituted system to analyze the properties of a TAF3/TRF3 complex in directing transcription initiation at the Myogenin promoter. Importantly, this new complex is required to replace the canonical TRID to recapitulate MyoD-dependent activation of Myogenin. In vitro and cell-based assays identify a domain of TAF3 that mediates coactivator functions targeted by MyoD. Our findings also suggest changes to CRSP/Mediator in terminally differentiated myotubes. This switching of the core promoter recognition complex during myogenesis allows a more balanced division of labor between activators and TAF coactivators, thus providing another strategy to accommodate cell-specific regulation during metazoan development.
引用
收藏
页码:96 / 105
页数:10
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