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