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Modeling dioxygenase enzyme kinetics in familial paraganglioma

Hypoxia inducible factors (HIFs) play vital roles in cellular maintenance of oxygen homeostasis. These transcription factors are responsible for the expression of genes involved in angiogenesis, metabolism, and cell proliferation. Here, we generate a detailed mathematical model for the enzyme kineti...

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Detalles Bibliográficos
Autores principales: Peters, Justin P., Her, Yeng F., Maher, L. James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610226/
https://www.ncbi.nlm.nih.gov/pubmed/26369930
http://dx.doi.org/10.1242/bio.013623
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author Peters, Justin P.
Her, Yeng F.
Maher, L. James
author_facet Peters, Justin P.
Her, Yeng F.
Maher, L. James
author_sort Peters, Justin P.
collection PubMed
description Hypoxia inducible factors (HIFs) play vital roles in cellular maintenance of oxygen homeostasis. These transcription factors are responsible for the expression of genes involved in angiogenesis, metabolism, and cell proliferation. Here, we generate a detailed mathematical model for the enzyme kinetics of α-ketoglutarate-dependent HIF prolyl 4-hydroxylase domain (PHD) dioxygenases to simulate our in vitro data showing synergistic PHD inhibition by succinate and hypoxia in experimental models of succinate dehydrogenase loss, which phenocopy familial paraganglioma. Our mathematical model confirms the inhibitory synergy of succinate and hypoxia under physiologically-relevant conditions. In agreement with our experimental data, the model predicts that HIF1α is not stabilized under atmospheric oxygen concentrations, as observed. Further, the model confirms that addition of α-ketoglutarate can reverse PHD inhibition by succinate and hypoxia in SDH-deficient cells.
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spelling pubmed-46102262015-10-27 Modeling dioxygenase enzyme kinetics in familial paraganglioma Peters, Justin P. Her, Yeng F. Maher, L. James Biol Open Research Article Hypoxia inducible factors (HIFs) play vital roles in cellular maintenance of oxygen homeostasis. These transcription factors are responsible for the expression of genes involved in angiogenesis, metabolism, and cell proliferation. Here, we generate a detailed mathematical model for the enzyme kinetics of α-ketoglutarate-dependent HIF prolyl 4-hydroxylase domain (PHD) dioxygenases to simulate our in vitro data showing synergistic PHD inhibition by succinate and hypoxia in experimental models of succinate dehydrogenase loss, which phenocopy familial paraganglioma. Our mathematical model confirms the inhibitory synergy of succinate and hypoxia under physiologically-relevant conditions. In agreement with our experimental data, the model predicts that HIF1α is not stabilized under atmospheric oxygen concentrations, as observed. Further, the model confirms that addition of α-ketoglutarate can reverse PHD inhibition by succinate and hypoxia in SDH-deficient cells. The Company of Biologists 2015-09-14 /pmc/articles/PMC4610226/ /pubmed/26369930 http://dx.doi.org/10.1242/bio.013623 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Peters, Justin P.
Her, Yeng F.
Maher, L. James
Modeling dioxygenase enzyme kinetics in familial paraganglioma
title Modeling dioxygenase enzyme kinetics in familial paraganglioma
title_full Modeling dioxygenase enzyme kinetics in familial paraganglioma
title_fullStr Modeling dioxygenase enzyme kinetics in familial paraganglioma
title_full_unstemmed Modeling dioxygenase enzyme kinetics in familial paraganglioma
title_short Modeling dioxygenase enzyme kinetics in familial paraganglioma
title_sort modeling dioxygenase enzyme kinetics in familial paraganglioma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610226/
https://www.ncbi.nlm.nih.gov/pubmed/26369930
http://dx.doi.org/10.1242/bio.013623
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