Suppr超能文献

缺氧诱导因子-3的研究进展:其结构、基因调控及生物学功能(综述)

Progress on hypoxia-inducible factor-3: Its structure, gene regulation and biological function (Review).

作者信息

Yang Sheng-Li, Wu Chao, Xiong Zhi-Fan, Fang Xiefan

机构信息

Department of General Surgery, Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430000, P.R. China.

Department of Medicine and Division of Digestion Disease, Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430077, P.R. China.

出版信息

Mol Med Rep. 2015 Aug;12(2):2411-6. doi: 10.3892/mmr.2015.3689. Epub 2015 Apr 27.

Abstract

Hypoxia inducible factors (HIFs) are transcription factors, which are commonly expressed in mammals, including humans. The HIFs consist of hypoxia-regulated α and oxygen-insensitive β subunits, and are key regulators of gene expression during hypoxia in normal and solid tumor tissues. Three members of the HIF family, HIF-1α, HIF-2α, and HIF-3α, are currently known. HIF-3α differs from HIF-1α and HIF-2α in protein structure and regulation of gene expression. For a long time, HIF-3α was considered as a negative mediator of HIF-regulated genes. HIF-3 has a transcriptional regulatory function, which negatively affects gene expression by competing with HIF-1α and HIF-2α in binding to transcriptional elements in target genes during hypoxia. Previously, certain target genes of HIF-3α have been identified, confirming the role of HIF-3α as a transcription factor. In this review, the protein structure, gene regulation and biological function of HIF-3 are discussed based on the literature.

摘要

缺氧诱导因子(HIFs)是转录因子,在包括人类在内的哺乳动物中普遍表达。HIFs由缺氧调节的α亚基和氧不敏感的β亚基组成,是正常组织和实体瘤组织缺氧时基因表达的关键调节因子。目前已知HIF家族的三个成员,即HIF-1α、HIF-2α和HIF-3α。HIF-3α在蛋白质结构和基因表达调控方面与HIF-1α和HIF-2α不同。长期以来,HIF-3α被认为是HIF调控基因的负性介质。HIF-3具有转录调节功能,在缺氧时通过与HIF-1α和HIF-2α竞争结合靶基因中的转录元件来负面影响基因表达。此前,已鉴定出HIF-3α的某些靶基因,证实了HIF-3α作为转录因子的作用。在本综述中,将基于文献讨论HIF-3的蛋白质结构、基因调控和生物学功能。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验