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缺氧诱导因子-1(HIF-1)的调控:来得不易,去得也难。

HIF-1 regulation: not so easy come, easy go.

作者信息

Yee Koh Mei, Spivak-Kroizman Taly R, Powis Garth

机构信息

Department of Experimental Therapeutics, M.D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Trends Biochem Sci. 2008 Nov;33(11):526-34. doi: 10.1016/j.tibs.2008.08.002. Epub 2008 Sep 21.

Abstract

The hypoxia-inducible factor-1 (HIF-1) is the master regulator of the cellular response to hypoxia and its expression levels are tightly controlled through synthesis and degradation. It is widely accepted that HIF-1alpha protein accumulation during hypoxia results from inhibition of its oxygen-dependent degradation by the von Hippel Lindau protein (pVHL) pathway. However, recent data describe new pVHL- or oxygen-independent mechanisms for HIF-1alpha degradation. Furthermore, the hypoxia-induced increase in HIF-1alpha levels is facilitated by the continued translation of HIF-1alpha during hypoxia despite the global inhibition of protein translation. Recent work has contributed to an increased understanding of the mechanisms that control the translation and degradation of HIF-1alpha under both normoxic and hypoxic conditions.

摘要

缺氧诱导因子-1(HIF-1)是细胞对缺氧反应的主要调节因子,其表达水平通过合成和降解受到严格控制。人们普遍认为,缺氧期间HIF-1α蛋白的积累是由于其通过冯·希佩尔-林道蛋白(pVHL)途径的氧依赖性降解受到抑制所致。然而,最近的数据描述了HIF-1α降解的新的不依赖pVHL或氧的机制。此外,尽管蛋白质翻译受到整体抑制,但缺氧期间HIF-1α的持续翻译促进了缺氧诱导的HIF-1α水平升高。最近的研究有助于加深对常氧和缺氧条件下控制HIF-1α翻译和降解机制的理解。

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