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线虫秀丽隐杆线虫中染色质重塑因子调控的小分子热休克蛋白 hsp-16.1 基因的缺氧诱导因子-1(HIF-1)非依赖性缺氧反应。

Hypoxia-inducible Factor-1 (HIF-1)-independent hypoxia response of the small heat shock protein hsp-16.1 gene regulated by chromatin-remodeling factors in the nematode Caenorhabditis elegans.

机构信息

Institute of Molecular Biology and Genetics, Research Center for Cellulomics, Department of Biological Sciences, World Class University Department of Biophysics and Chemical Biology, Seoul National University, Seoul 151-742, South Korea.

出版信息

J Biol Chem. 2013 Jan 18;288(3):1582-9. doi: 10.1074/jbc.M112.401554. Epub 2012 Dec 10.

Abstract

Oxygen deprivation is accompanied by the coordinated expression of numerous hypoxia-responsive genes, many of which are controlled by hypoxia-inducible factor-1 (HIF-1). However, the cellular response to hypoxia is not likely to be mediated by HIF-1 alone, and little is known about HIF-1-independent hypoxia responses. To better establish the molecular mechanisms of HIF-1-independent hypoxia responses, we sought to characterize the molecular basis of the hypoxia response of the hsp-16.1 gene in the nematode Caenorhabditis elegans; this gene has been shown to be induced by hypoxia independently of hif-1. Using affinity purification followed by LC-MS/MS, we identified HMG-1.2 as a protein that binds to a specific promoter region under hypoxic conditions. By systematic prediction followed by validation of these interactions through RNAi, we identified the chromatin modifiers isw-1 and hda-1, histone H4, and NURF-1 chromatin-remodeling factors as new components of the hif-1-independent hypoxia response. These data suggest that the modulation of nucleosome positioning at the hsp-16.1 promoter may be important for the hypoxia response. In addition, we found that calcineurin acts independently of hif-1 to modulate the cellular response to hypoxia and that calcium ions are necessary for the induction of hsp-16.1 under hypoxic conditions.

摘要

缺氧伴随着众多缺氧反应基因的协调表达,其中许多基因受缺氧诱导因子-1(HIF-1)控制。然而,细胞对缺氧的反应不太可能仅由 HIF-1 介导,并且对 HIF-1 不依赖的缺氧反应知之甚少。为了更好地建立 HIF-1 不依赖的缺氧反应的分子机制,我们试图描述线虫秀丽隐杆线虫中 hsp-16.1 基因的缺氧反应的分子基础;该基因已被证明可独立于 hif-1 被缺氧诱导。通过亲和纯化后进行 LC-MS/MS 分析,我们鉴定出 HMG-1.2 是一种在缺氧条件下与特定启动子区域结合的蛋白质。通过系统预测并通过 RNAi 验证这些相互作用,我们鉴定出染色质修饰剂 isw-1 和 hda-1、组蛋白 H4 和 NURF-1 染色质重塑因子是 HIF-1 不依赖的缺氧反应的新组成部分。这些数据表明,核小体在 hsp-16.1 启动子上的定位的调节可能对缺氧反应很重要。此外,我们发现钙调神经磷酸酶独立于 HIF-1 调节细胞对缺氧的反应,并且钙离子是在缺氧条件下诱导 hsp-16.1 的必要条件。

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