Frost Julianty, Frost Mark, Batie Michael, Jiang Hao, Rocha Sonia
Department of Molecular Physiology and Cell Signalling, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 7ZB, UK.
Centre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.
Cancers (Basel). 2021 Jan 19;13(2):350. doi: 10.3390/cancers13020350.
Hypoxia-reduction in oxygen availability-plays key roles in both physiological and pathological processes. Given the importance of oxygen for cell and organism viability, mechanisms to sense and respond to hypoxia are in place. A variety of enzymes utilise molecular oxygen, but of particular importance to oxygen sensing are the 2-oxoglutarate (2-OG) dependent dioxygenases (2-OGDs). Of these, Prolyl-hydroxylases have long been recognised to control the levels and function of Hypoxia Inducible Factor (HIF), a master transcriptional regulator in hypoxia, via their hydroxylase activity. However, recent studies are revealing that dioxygenases are involved in almost all aspects of gene regulation, including chromatin organisation, transcription and translation. We highlight the relevance of HIF and 2-OGDs in the control of gene expression in response to hypoxia and their relevance to human biology and health.
缺氧——即氧气可利用性降低——在生理和病理过程中都起着关键作用。鉴于氧气对细胞和生物体生存能力的重要性,感知和应对缺氧的机制已然存在。多种酶利用分子氧,但对氧感知特别重要的是2-氧代戊二酸(2-OG)依赖性双加氧酶(2-OGD)。其中,脯氨酰羟化酶长期以来被认为通过其羟化酶活性来控制缺氧诱导因子(HIF)的水平和功能,HIF是缺氧状态下的主要转录调节因子。然而,最近的研究表明,双加氧酶几乎参与基因调控的各个方面,包括染色质组织、转录和翻译。我们强调了HIF和2-OGD在响应缺氧时对基因表达的控制中的相关性,以及它们与人类生物学和健康的相关性。