Biotechnology Research Institute, Molecular Neuroscience Center, and Department of Biochemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.
Curr Mol Pharmacol. 2009 Jan;2(1):19-31. doi: 10.2174/1874467210902010019.
Lessons from viral hijacks of cells and cancer biology suggest that the activation of G protein-coupled receptors (GPCRs) often results in the modulation of various transcription factors and cofactors. Since drugs acting on GPCRs represent a significant portion of therapeutic agents currently in use, it is important to understand the actions of GPCRs on gene expression. GPCRs and their associated heterotrimeric G proteins are known to regulate gene transcription through complex signaling networks. The G protein-mediated signaling cascades have been extensively studied and accumulating evidence indicates that the four subfamilies of G proteins may utilize both common and unique pathways for transcriptional regulation. This review aims to provide a contemporary account of our understanding on the regulation of transcription factors by GPCRs, with a special emphasis on specific regulations of transcription factors such as STAT3 and NF-kappaB by individual G protein subfamilies. Functional impacts of the signal integration between different pathways and the contributions by other GPCR-interacting molecules will also be briefly discussed.
病毒劫持细胞和癌症生物学的教训表明,G 蛋白偶联受体 (GPCR) 的激活通常会导致各种转录因子和辅助因子的调节。由于作用于 GPCR 的药物代表了目前使用的治疗药物的重要部分,因此了解 GPCR 对基因表达的作用非常重要。众所周知,GPCR 及其相关的异三聚体 G 蛋白通过复杂的信号网络调节基因转录。G 蛋白介导的信号级联已被广泛研究,越来越多的证据表明,G 蛋白的四个亚家族可能利用转录调控的共同和独特途径。本综述旨在提供对 GPCR 调节转录因子的现代理解,特别强调 G 蛋白亚家族对转录因子(如 STAT3 和 NF-κB)的特定调节。还将简要讨论不同途径之间信号整合的功能影响以及其他与 GPCR 相互作用的分子的贡献。