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转录因子的异三聚 G 蛋白调节。

Regulation of transcription factors by heterotrimeric G proteins.

机构信息

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.

出版信息

Curr Mol Pharmacol. 2009 Jan;2(1):19-31. doi: 10.2174/1874467210902010019.

Abstract

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.

摘要

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。

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