Taatjes Dylan J, Tjian Robert
Howard Hughes Medical Institute, Department of Molecular and Cell Biology, 401 Barker Hall, University of California-Berkeley, Berkeley, CA 94720, USA.
Mol Cell. 2004 Jun 4;14(5):675-83. doi: 10.1016/j.molcel.2004.05.014.
The multi-subunit, human CRSP coactivator-also known as Mediator (Med)-regulates transcription by mediating signals between enhancer-bound factors (activators) and the core transcriptional machinery. Interestingly, different activators are known to bind distinct subunits within the CRSP/Med complex. We have isolated a stable, endogenous CRSP/Med complex (CRSP/Med2) that specifically lacks both the Med220 and the Med70 subunits. The three-dimensional structure of CRSP/Med2 was determined to 31 A resolution using electron microscopy and single-particle reconstruction techniques. Despite lacking both Med220 and Med70, CRSP/Med2 displays potent, activator-dependent transcriptional coactivator function in response to VP16, Sp1, and Sp1/SREBP-1a in vitro using chromatin templates. However, CRSP/Med2 is unable to potentiate activated transcription from a vitamin D receptor-responsive promoter, which requires interaction with Med220 for coactivator recruitment, whereas VDR-directed activation by CRSP/Med occurs normally. Thus, it appears that CRSP/Med may be regulated by a combinatorial assembly mechanism that allows promoter-selective function upon exchange of specific coactivator targets.
多亚基人CRSP共激活因子——也被称为中介体(Med)——通过介导增强子结合因子(激活因子)与核心转录机制之间的信号来调节转录。有趣的是,已知不同的激活因子会结合CRSP/Med复合物中的不同亚基。我们分离出了一种稳定的内源性CRSP/Med复合物(CRSP/Med2),它特异性地缺乏Med220和Med70亚基。利用电子显微镜和单颗粒重建技术,确定了CRSP/Med2的三维结构,分辨率为31埃。尽管缺乏Med220和Med70,但在体外使用染色质模板时,CRSP/Med2对VP16、Sp1和Sp1/SREBP-1a显示出有效的、依赖激活因子的转录共激活功能。然而,CRSP/Med2无法增强维生素D受体反应性启动子的激活转录,而该启动子需要与Med220相互作用以募集共激活因子,而CRSP/Med介导的VDR定向激活则正常发生。因此,似乎CRSP/Med可能受组合组装机制调控,该机制允许在交换特定共激活因子靶点时实现启动子选择性功能。