SOD2
超氧化物歧化酶
缺氧诱导因子
转录因子
超氧化物
癌症研究
缺氧诱导因子1
染色质免疫沉淀
TFAM公司
缺氧(环境)
生物
细胞生物学
分子生物学
化学
基因表达
酶
生物化学
发起人
氧气
基因
有机化学
作者
Yaohui Gao,Caixia Li,Shao-Ming Shen,Hui Li,Guo‐Qiang Chen,Qing Wei,Li‐Shun Wang
标识
DOI:10.1016/j.bbrc.2013.04.034
摘要
Hypoxia-inducible factor 1α (HIF-1α) is an oxygen-sensitive subunit of HIF-1, the master transcription factor for cellular response to hypoxia. Down-regulation of the mitochondrial enzyme superoxide dismutase 2 (SOD2) contributes to the stabilization of HIF-1α under hypoxia due to the decreased dismutation of superoxide radical. Here we report that HIF-1α could also regulate the expression of SOD2. We found that both stabilization of HIF-1α expression under nomoxia caused by pVHL deficiency and hypoxia treatment significantly reduced SOD2 expression, and shRNAs specifically against HIF-1α restored SOD2 expression in both circumstances. Further analyses with luciferase reporter assay and chromatin immunoprecipitation assay revealed that HIF-1α inhibited and directly bound to the hypoxia-responsive element in SOD2 promoter. These findings indicated the existence of a positive feedback between HIF-1α and SOD2 and provided new clues for understanding the molecular mechanisms of hypoxia adaptation.
科研通智能强力驱动
Strongly Powered by AbleSci AI