Zheng Yingfeng, Murphy Leigh C
Department of Biochemistry and Medical Genetics (YZ, LCM), University of Manitoba; Manitoba Institute of Cell Biology (YZ, LCM), CancerCare Manitoba, Winnipeg, Manitoba, Canada.
Nucl Recept Signal. 2016 Jan 13;14:e001. doi: 10.1621/nrs.14001. eCollection 2016.
Cell cycle progression is tightly controlled by several kinase families including Cyclin-Dependent Kinases, Polo-Like Kinases, and Aurora Kinases. A large amount of data show that steroid hormone receptors and various components of the cell cycle, including cell cycle regulated kinases, interact, and this often results in altered transcriptional activity of the receptor. Furthermore, steroid hormones, through their receptors, can also regulate the transcriptional expression of genes that are required for cell cycle regulation. However, emerging data suggest that steroid hormone receptors may have roles in cell cycle progression independent of their transcriptional activity. The following is a review of how steroid receptors and their coregulators can regulate or be regulated by the cell cycle machinery, with a particular focus on roles independent of transcription in G2/M.
细胞周期进程受到包括细胞周期蛋白依赖性激酶、波罗样激酶和极光激酶在内的多个激酶家族的严格控制。大量数据表明,类固醇激素受体与细胞周期的各种成分相互作用,包括细胞周期调节激酶,这通常会导致受体转录活性的改变。此外,类固醇激素通过其受体,还可以调节细胞周期调节所需基因的转录表达。然而,新出现的数据表明,类固醇激素受体可能在细胞周期进程中发挥作用,而与其转录活性无关。以下是一篇关于类固醇受体及其共调节因子如何被细胞周期机制调节或反之调节的综述,特别关注在G2/M期独立于转录的作用。