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Chromatin as an oxygen sensor and active player in the hypoxia response

Changes in the availability or demand for oxygen induce dramatic changes at the cellular level. Primarily, activation of a family of oxygen labile transcription factors, Hypoxia Inducible Factor (HIF), initiates a variety of cellular processes required to re-instate oxygen homeostasis. Oxygen is sen...

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Detalles Bibliográficos
Autores principales: Melvin, Andrew, Rocha, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476533/
https://www.ncbi.nlm.nih.gov/pubmed/21924352
http://dx.doi.org/10.1016/j.cellsig.2011.08.019
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author Melvin, Andrew
Rocha, Sonia
author_facet Melvin, Andrew
Rocha, Sonia
author_sort Melvin, Andrew
collection PubMed
description Changes in the availability or demand for oxygen induce dramatic changes at the cellular level. Primarily, activation of a family of oxygen labile transcription factors, Hypoxia Inducible Factor (HIF), initiates a variety of cellular processes required to re-instate oxygen homeostasis. Oxygen is sensed by molecular dioxygenases in cells, such as the prolyl-hydroxylases (PHDs), enzymes which are responsible for the oxygen-dependent regulation of HIF. As HIF is a transcription factor it must bind DNA sequences of its target genes possibly in the context of a complex chromatin structure. How chromatin structure changes in response to hypoxia is currently unknown. However, the identification of a novel class of histone demethylases as true dioxygenases suggests that chromatin can act as an oxygen sensor and plays an active role in the coordination of the cellular response to hypoxia. This review will discuss the current knowledge on how hypoxia engages with different proteins involved in chromatin organisation and dynamics.
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spelling pubmed-34765332012-10-19 Chromatin as an oxygen sensor and active player in the hypoxia response Melvin, Andrew Rocha, Sonia Cell Signal Review Changes in the availability or demand for oxygen induce dramatic changes at the cellular level. Primarily, activation of a family of oxygen labile transcription factors, Hypoxia Inducible Factor (HIF), initiates a variety of cellular processes required to re-instate oxygen homeostasis. Oxygen is sensed by molecular dioxygenases in cells, such as the prolyl-hydroxylases (PHDs), enzymes which are responsible for the oxygen-dependent regulation of HIF. As HIF is a transcription factor it must bind DNA sequences of its target genes possibly in the context of a complex chromatin structure. How chromatin structure changes in response to hypoxia is currently unknown. However, the identification of a novel class of histone demethylases as true dioxygenases suggests that chromatin can act as an oxygen sensor and plays an active role in the coordination of the cellular response to hypoxia. This review will discuss the current knowledge on how hypoxia engages with different proteins involved in chromatin organisation and dynamics. Elsevier Science Ltd 2012-01 /pmc/articles/PMC3476533/ /pubmed/21924352 http://dx.doi.org/10.1016/j.cellsig.2011.08.019 Text en © 2012 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Review
Melvin, Andrew
Rocha, Sonia
Chromatin as an oxygen sensor and active player in the hypoxia response
title Chromatin as an oxygen sensor and active player in the hypoxia response
title_full Chromatin as an oxygen sensor and active player in the hypoxia response
title_fullStr Chromatin as an oxygen sensor and active player in the hypoxia response
title_full_unstemmed Chromatin as an oxygen sensor and active player in the hypoxia response
title_short Chromatin as an oxygen sensor and active player in the hypoxia response
title_sort chromatin as an oxygen sensor and active player in the hypoxia response
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476533/
https://www.ncbi.nlm.nih.gov/pubmed/21924352
http://dx.doi.org/10.1016/j.cellsig.2011.08.019
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