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缺氧诱导因子1α的羧基末端反式激活活性由一种不依赖于冯·希佩尔-林道蛋白、受羟基化调节的与p300/CBP的结合所调控。

Carboxyl-terminal transactivation activity of hypoxia-inducible factor 1 alpha is governed by a von Hippel-Lindau protein-independent, hydroxylation-regulated association with p300/CBP.

作者信息

Sang Nianli, Fang Jie, Srinivas Vickram, Leshchinsky Irene, Caro Jaime

机构信息

Cardeza Foundation for Hematologic Research, Department of Medicine, Jefferson Medical College of Thomas Jefferson University, Philadelphia, Pennsylvania 19107-5099, USA.

出版信息

Mol Cell Biol. 2002 May;22(9):2984-92. doi: 10.1128/MCB.22.9.2984-2992.2002.

Abstract

Hypoxia-inducible factor 1 complex (HIF-1) plays a pivotal role in oxygen homeostasis and adaptation to hypoxia. Its function is controlled by both the protein stability and the transactivation activity of its alpha subunit, HIF-1 alpha. Hydroxylation of at least two prolyl residues in the oxygen-dependent degradation domain of HIF-1 alpha regulates its interaction with the von Hippel-Lindau protein (VHL) that targets HIF-1 alpha for ubiquitination and proteasomal degradation. Several prolyl hydroxylases have been found to specifically hydroxylate HIF-1 alpha. In this report, we investigated possible roles of VHL and hydroxylases in the regulation of the transactivation activity of the C-terminal activating domain (CAD) of HIF-1 alpha. We demonstrate that regulation of the transactivation activity of HIF-1 alpha CAD also involves hydroxylase activity but does not require functional VHL. In addition, stimulation of the CAD activity by a hydroxylase inhibitor, hypoxia, and desferrioxamine was severely blocked by the adenoviral oncoprotein E1A but not by an E1A mutant defective in targeting p300/CBP. We further demonstrate that a hydroxylase inhibitor, hypoxia, and desferrioxamine promote the functional and physical interaction between HIF-1 alpha CAD and p300/CBP in vivo. Taken together, our data provide evidence that hypoxia-regulated stabilization and transcriptional stimulation of HIF-1 alpha function are regulated through partially overlapping but distinguishable pathways.

摘要

缺氧诱导因子1复合物(HIF-1)在氧稳态及对缺氧的适应过程中发挥着关键作用。其功能受α亚基HIF-1α的蛋白质稳定性和反式激活活性的控制。HIF-1α的氧依赖降解结构域中至少两个脯氨酰残基的羟基化作用调节其与冯·希佩尔-林道蛋白(VHL)的相互作用,VHL将HIF-1α靶向泛素化和蛋白酶体降解。已发现几种脯氨酰羟化酶可特异性地使HIF-1α羟基化。在本报告中,我们研究了VHL和羟化酶在调节HIF-1α C末端激活结构域(CAD)反式激活活性中的可能作用。我们证明,HIF-1α CAD反式激活活性的调节也涉及羟化酶活性,但不需要功能性VHL。此外,羟化酶抑制剂、缺氧和去铁胺对CAD活性的刺激被腺病毒癌蛋白E1A严重阻断,但未被靶向p300/CBP缺陷的E1A突变体阻断。我们进一步证明,羟化酶抑制剂、缺氧和去铁胺在体内促进HIF-1α CAD与p300/CBP之间的功能和物理相互作用。综上所述,我们的数据提供了证据,表明缺氧调节的HIF-1α功能的稳定化和转录刺激是通过部分重叠但可区分的途径进行调节的。

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