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TOR 信号的进化保守调控。

Evolutionarily conserved regulation of TOR signalling.

机构信息

Institute of Molecular and Cellular Biosciences, The University of Tokyo, Japan.

出版信息

J Biochem. 2013 Jul;154(1):1-10. doi: 10.1093/jb/mvt047. Epub 2013 May 21.

Abstract

The target of rapamycin (TOR) is an evolutionarily conserved protein kinase that regulates cell growth in response to various environmental as well as intracellular cues through the formation of 2 distinct TOR complexes (TORC), TORC1 and TORC2. Dysregulation of TORC1 and TORC2 activity is closely associated with various diseases, including diabetes, cancer and neurodegenerative disorders. Over the past few years, new regulatory mechanisms of TORC1 and TORC2 activity have been elucidated. Furthermore, recent advances in the study of TOR inhibitors have revealed previously unrecognized cellular functions of TORC1. In this review, we briefly summarize the current understanding of the evolutionarily conserved TOR signalling from upstream regulators to downstream events.

摘要

雷帕霉素靶蛋白(TOR)是一种进化上保守的蛋白激酶,通过形成 2 种不同的 TOR 复合物(TORC1 和 TORC2),响应各种环境和细胞内信号来调节细胞生长。TORC1 和 TORC2 活性的失调与多种疾病密切相关,包括糖尿病、癌症和神经退行性疾病。在过去的几年中,已经阐明了 TORC1 和 TORC2 活性的新调节机制。此外,对 TOR 抑制剂的研究进展揭示了 TORC1 的以前未被识别的细胞功能。在这篇综述中,我们简要总结了从上游调节剂到下游事件的进化上保守的 TOR 信号转导的最新认识。

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