Weigel N L, Moore N L
Department of Molecular and Cellular Biology, 1 Baylor Plaza, Baylor College of Medicine, Houston, TX 77030, United States.
Mol Cell Endocrinol. 2007 Feb;265-266:157-61. doi: 10.1016/j.mce.2006.12.013. Epub 2007 Jan 5.
Steroid receptors (SR), which are ligand activated transcription factors, and their coactivators are phosphoproteins whose activities are regulated by cell signaling pathways. Many of the identified phosphorylation sites in these proteins contain Ser/Thr-Pro motifs suggesting that they are substrates for cyclin dependent kinases and/or for mitogen activated protein kinases. An analysis of the roles of cyclins and their kinases in regulating receptor action has revealed that there are both stimulatory and inhibitory actions of cyclins, that some of the actions are independent of the partner kinases and that these activities are receptor specific. Consistent with this finding, the limited analyses of receptor activity as a function of cell cycle reveal distinct patterns of activation. SR often regulate cell proliferation. Thus, the cross-talk between cyclins and their kinases and the SR provides a means for integrating the actions of the SR with the cell cycle status of cells.
类固醇受体(SR)是配体激活的转录因子,其共激活因子是磷蛋白,其活性受细胞信号通路调节。这些蛋白质中许多已确定的磷酸化位点含有丝氨酸/苏氨酸-脯氨酸基序,表明它们是细胞周期蛋白依赖性激酶和/或丝裂原活化蛋白激酶的底物。对细胞周期蛋白及其激酶在调节受体作用中的作用分析表明,细胞周期蛋白既有刺激作用也有抑制作用,其中一些作用独立于伴侣激酶,且这些活性具有受体特异性。与这一发现一致,作为细胞周期函数的受体活性的有限分析揭示了不同的激活模式。SR通常调节细胞增殖。因此,细胞周期蛋白及其激酶与SR之间的相互作用为将SR的作用与细胞的细胞周期状态整合提供了一种手段。