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Gene transcription and chromatin regulation in hypoxia

Oxygen sensing is an essential feature of metazoan biology and reductions in oxygen availability (hypoxia) have both physiological and pathophysiological implications. Co-ordinated mechanisms have evolved for sensing and responding to hypoxia, which involve diverse biological outputs, with the main...

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Detalles Bibliográficos
Autores principales: Batie, Michael, Rocha, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329336/
https://www.ncbi.nlm.nih.gov/pubmed/32369557
http://dx.doi.org/10.1042/BST20191106
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author Batie, Michael
Rocha, Sonia
author_facet Batie, Michael
Rocha, Sonia
author_sort Batie, Michael
collection PubMed
description Oxygen sensing is an essential feature of metazoan biology and reductions in oxygen availability (hypoxia) have both physiological and pathophysiological implications. Co-ordinated mechanisms have evolved for sensing and responding to hypoxia, which involve diverse biological outputs, with the main aim of restoring oxygen homeostasis. This includes a dynamic gene transcriptional response, the central drivers of which are the hypoxia-inducible factor (HIF) family of transcription factors. HIFs are regulated in an oxygen-dependent manner and while their role in hypoxia is well established, it is apparent that other key players are required for gene expression control in hypoxia. In this review, we highlight the current understanding of the known and potential molecular mechanisms underpinning gene transcriptional responses to hypoxia in mammals, with a focus on oxygen-dependent effects on chromatin structure.
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spelling pubmed-73293362020-07-13 Gene transcription and chromatin regulation in hypoxia Batie, Michael Rocha, Sonia Biochem Soc Trans Review Articles Oxygen sensing is an essential feature of metazoan biology and reductions in oxygen availability (hypoxia) have both physiological and pathophysiological implications. Co-ordinated mechanisms have evolved for sensing and responding to hypoxia, which involve diverse biological outputs, with the main aim of restoring oxygen homeostasis. This includes a dynamic gene transcriptional response, the central drivers of which are the hypoxia-inducible factor (HIF) family of transcription factors. HIFs are regulated in an oxygen-dependent manner and while their role in hypoxia is well established, it is apparent that other key players are required for gene expression control in hypoxia. In this review, we highlight the current understanding of the known and potential molecular mechanisms underpinning gene transcriptional responses to hypoxia in mammals, with a focus on oxygen-dependent effects on chromatin structure. Portland Press Ltd. 2020-06-30 2020-05-05 /pmc/articles/PMC7329336/ /pubmed/32369557 http://dx.doi.org/10.1042/BST20191106 Text en © 2020 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of the University of Liverpool in an all-inclusive Read and Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC.
spellingShingle Review Articles
Batie, Michael
Rocha, Sonia
Gene transcription and chromatin regulation in hypoxia
title Gene transcription and chromatin regulation in hypoxia
title_full Gene transcription and chromatin regulation in hypoxia
title_fullStr Gene transcription and chromatin regulation in hypoxia
title_full_unstemmed Gene transcription and chromatin regulation in hypoxia
title_short Gene transcription and chromatin regulation in hypoxia
title_sort gene transcription and chromatin regulation in hypoxia
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329336/
https://www.ncbi.nlm.nih.gov/pubmed/32369557
http://dx.doi.org/10.1042/BST20191106
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