Nettles Kendall W, Greene Geoffrey L
The University of Chicago, The Ben May Institute for Cancer Research, Chicago, Illinois 60637, USA.
Annu Rev Physiol. 2005;67:309-33. doi: 10.1146/annurev.physiol.66.032802.154710.
Nuclear receptors modulate transcription through ligand-mediated recruitment of transcriptional coregulator proteins. The structural connection between ligand and coregulator is mediated by a molecular switch, made up of the most carboxy-terminal helix in the ligand-binding domain, helix 12. The dynamics of this switch are thought to underlie ligand specificity of nuclear receptor signaling, but the details of this control mechanism have remained elusive. This review highlights recent structural work on how the ligand controls this molecular switch and the modulation of this signaling pathway by receptor subtype and dimer partner.
核受体通过配体介导的转录共调节蛋白募集来调节转录。配体与共调节因子之间的结构联系由一个分子开关介导,该开关由配体结合域中最羧基末端的螺旋(螺旋12)组成。这个开关的动力学被认为是核受体信号传导配体特异性的基础,但这种控制机制的细节仍然难以捉摸。这篇综述重点介绍了关于配体如何控制这个分子开关以及受体亚型和二聚体伙伴对该信号通路调节的最新结构研究。