Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The hypoxia-inducible factors are α,β-heterodimeric transcription factors that mediate the chronic response to hypoxia in humans and other animals. Protein hydroxylases belonging to two different structural subfamilies of the Fe(II) and 2-oxoglutarate (2OG)-dependent oxygenase superfamily modify HIFα. HIFα prolyl-hydroxylation, as catalysed by the PHDs, regulates HIFα levels and, consequently, α,β-HIF levels. HIFα asparaginyl-hydroxylation, as catalysed by factor inhibiting HIF (FIH), regulates the transcriptional activity of α,β-HIF. The activities of the PHDs and FIH are regulated by O2 availability, enabling them to act as hypoxia sensors. We provide an overview of the biochemistry of the HIF hydroxylases, discussing evidence that their kinetic and structural properties may be tuned to their roles in the HIF system. Avenues for future research and therapeutic modulation are discussed.

More information Original publication

DOI

10.1016/j.cbpa.2024.102428

Type

Journal article

Publication Date

2024-04-01T00:00:00+00:00

Volume

79

Keywords

Ankyrin repeat domain, Asparaginyl hydroxylase, Epigenetics, Factor inhibiting HIF (FIH), HIF prolyl-hydroxylases (PHDs/EGLNs), Hypoxia-inducible factor (HIF), JmjC demethylases, JmjC histone demethylases (JmjC KDMs), Oxygen/hypoxia sensing, Animals, Humans, Mixed Function Oxygenases, Transcription Factors, Hypoxia, Hydroxylation