| Literature DB >> 25832587 |
Rebecca L Hancock1,2, Kate Dunne1,2, Louise J Walport1, Emily Flashman1, Akane Kawamura1,2.
Abstract
The response to hypoxia is primarily mediated by the hypoxia-inducible transcription factor (HIF). Levels of HIF are regulated by the oxygen-sensing HIF hydroxylases, members of the 2-oxoglutarate (2OG) dependent oxygenase family. JmjC-domain containing histone lysine demethylases (JmjC-KDMs), also members of the 2OG oxygenase family, are key epigenetic regulators that modulate the methylation levels of histone tails. Kinetic studies of the JmjC-KDMs indicate they could also act in an oxygen-sensitive manner. This may have important implications for epigenetic regulation in hypoxia. In this review we examine evidence that the levels and activity of JmjC-KDMs are sensitive to oxygen availability, and consider how this may influence their roles in early development and hypoxic disease states including cancer and cardiovascular disease.Entities:
Keywords: 2-oxoglutarate dependent oxygenases; H3; HIF; KDMs; cancer; cardiovascular diseases; development; epigenetic regulation; histone 3; histone demethylases; hypoxia; oxygen kinetics; oxygen sensors
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Year: 2015 PMID: 25832587 DOI: 10.2217/epi.15.24
Source DB: PubMed Journal: Epigenomics ISSN: 1750-192X Impact factor: 4.778