Wallberg Annika E, Yamamura Soichiro, Malik Sohail, Spiegelman Bruce M, Roeder Robert G
Laboratory of Biochemistry and Molecular Biology, The Rockefeller University, New York, NY 10021, USA.
Mol Cell. 2003 Nov;12(5):1137-49. doi: 10.1016/s1097-2765(03)00391-5.
Transcriptional coactivators showing physical and functional interactions with PPARgamma include the protein acetyl transferase p300, the TRAP/Mediator complex that interacts with the general transcription machinery, and the highly regulated PGC-1alpha. We show that PGC-1alpha directly interacts with TRAP/Mediator, through the PPARgamma-interacting subunit TRAP220, and stimulates TRAP/Mediator-dependent function on DNA templates. Further, while ineffective by itself, PGC-1alpha stimulates p300-dependent histone acetylation and transcription on chromatin templates in response to PPARgamma. These functions are mediated by largely independent PPARgamma, p300, and TRAP220 interaction domains in PGC-1alpha, whereas p300 and TRAP220 show ligand-dependent interactions with a common region of PPARgamma. Apart from showing PGC-1alpha functions both in chromatin remodeling and in preinitiation complex formation or function (transcription), these results suggest a key role for PGC-1alpha, through concerted but dynamic interactions, in coordinating these steps.
与PPARγ表现出物理和功能相互作用的转录共激活因子包括蛋白质乙酰转移酶p300、与通用转录机制相互作用的TRAP/中介体复合物,以及受到高度调控的PGC-1α。我们发现,PGC-1α通过与PPARγ相互作用的亚基TRAP220直接与TRAP/中介体相互作用,并刺激TRAP/中介体在DNA模板上发挥依赖其自身的功能。此外,虽然PGC-1α本身没有作用,但它能响应PPARγ刺激p300依赖的组蛋白乙酰化以及染色质模板上的转录。这些功能主要由PGC-1α中独立的PPARγ、p300和TRAP220相互作用结构域介导,而p300和TRAP220与PPARγ的一个共同区域表现出依赖配体的相互作用。除了表明PGC-1α在染色质重塑以及起始前复合物形成或功能(转录)方面均发挥作用外,这些结果还表明,PGC-1α通过协同但动态的相互作用,在协调这些步骤中起着关键作用。