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Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)

Human 2-oxoglutarate oxygenases catalyse a range of biological oxidations including the demethylation of histone and nucleic acid substrates and the hydroxylation of proteins and small molecules. Some of these processes are centrally involved in regulation of cellular responses to hypoxia. The ALKBH...

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Autores principales: Thalhammer, Armin, Bencokova, Zuzana, Poole, Rachel, Loenarz, Christoph, Adam, Julie, O'Flaherty, Linda, Schödel, Johannes, Mole, David, Giaslakiotis, Konstantinos, Schofield, Christopher J., Hammond, Ester M., Ratcliffe, Peter J., Pollard, Patrick J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021549/
https://www.ncbi.nlm.nih.gov/pubmed/21264265
http://dx.doi.org/10.1371/journal.pone.0016210
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author Thalhammer, Armin
Bencokova, Zuzana
Poole, Rachel
Loenarz, Christoph
Adam, Julie
O'Flaherty, Linda
Schödel, Johannes
Mole, David
Giaslakiotis, Konstantinos
Schofield, Christopher J.
Hammond, Ester M.
Ratcliffe, Peter J.
Pollard, Patrick J.
author_facet Thalhammer, Armin
Bencokova, Zuzana
Poole, Rachel
Loenarz, Christoph
Adam, Julie
O'Flaherty, Linda
Schödel, Johannes
Mole, David
Giaslakiotis, Konstantinos
Schofield, Christopher J.
Hammond, Ester M.
Ratcliffe, Peter J.
Pollard, Patrick J.
author_sort Thalhammer, Armin
collection PubMed
description Human 2-oxoglutarate oxygenases catalyse a range of biological oxidations including the demethylation of histone and nucleic acid substrates and the hydroxylation of proteins and small molecules. Some of these processes are centrally involved in regulation of cellular responses to hypoxia. The ALKBH proteins are a sub-family of 2OG oxygenases that are defined by homology to the Escherichia coli DNA-methylation repair enzyme AlkB. Here we report evidence that ALKBH5 is probably unique amongst the ALKBH genes in being a direct transcriptional target of hypoxia inducible factor-1 (HIF-1) and is induced by hypoxia in a range of cell types. We show that purified recombinant ALKBH5 is a bona fide 2OG oxygenase that catalyses the decarboxylation of 2OG but appears to have different prime substrate requirements from those so far defined for other ALKBH family members. Our findings define a new class of HIF-transcriptional target gene and suggest that ALKBH5 may have a role in the regulation of cellular responses to hypoxia.
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spelling pubmed-30215492011-01-24 Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α) Thalhammer, Armin Bencokova, Zuzana Poole, Rachel Loenarz, Christoph Adam, Julie O'Flaherty, Linda Schödel, Johannes Mole, David Giaslakiotis, Konstantinos Schofield, Christopher J. Hammond, Ester M. Ratcliffe, Peter J. Pollard, Patrick J. PLoS One Research Article Human 2-oxoglutarate oxygenases catalyse a range of biological oxidations including the demethylation of histone and nucleic acid substrates and the hydroxylation of proteins and small molecules. Some of these processes are centrally involved in regulation of cellular responses to hypoxia. The ALKBH proteins are a sub-family of 2OG oxygenases that are defined by homology to the Escherichia coli DNA-methylation repair enzyme AlkB. Here we report evidence that ALKBH5 is probably unique amongst the ALKBH genes in being a direct transcriptional target of hypoxia inducible factor-1 (HIF-1) and is induced by hypoxia in a range of cell types. We show that purified recombinant ALKBH5 is a bona fide 2OG oxygenase that catalyses the decarboxylation of 2OG but appears to have different prime substrate requirements from those so far defined for other ALKBH family members. Our findings define a new class of HIF-transcriptional target gene and suggest that ALKBH5 may have a role in the regulation of cellular responses to hypoxia. Public Library of Science 2011-01-14 /pmc/articles/PMC3021549/ /pubmed/21264265 http://dx.doi.org/10.1371/journal.pone.0016210 Text en Thallhammer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Thalhammer, Armin
Bencokova, Zuzana
Poole, Rachel
Loenarz, Christoph
Adam, Julie
O'Flaherty, Linda
Schödel, Johannes
Mole, David
Giaslakiotis, Konstantinos
Schofield, Christopher J.
Hammond, Ester M.
Ratcliffe, Peter J.
Pollard, Patrick J.
Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)
title Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)
title_full Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)
title_fullStr Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)
title_full_unstemmed Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)
title_short Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)
title_sort human alkb homologue 5 is a nuclear 2-oxoglutarate dependent oxygenase and a direct target of hypoxia-inducible factor 1α (hif-1α)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021549/
https://www.ncbi.nlm.nih.gov/pubmed/21264265
http://dx.doi.org/10.1371/journal.pone.0016210
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