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Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation

Prolyl hydroxylase domain protein 2 (PHD2) belongs to an evolutionarily conserved superfamily of 2-oxoglutarate and Fe(II)-dependent dioxygenases that mediates homeostatic responses to oxygen deprivation by mediating hypoxia-inducible factor-1α (HIF-1α) hydroxylation and degradation. Although oxidat...

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Autores principales: Lee, Gibok, Won, Hyung-Sik, Lee, Yoon-Mi, Choi, Jae-Wan, Oh, Taek-In, Jang, Jeong-Hwa, Choi, Dong-Kug, Lim, Beong-Ou, Kim, Young Jun, Park, Jong-Wan, Puigserver, Pere, Lim, Ji-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4703963/
https://www.ncbi.nlm.nih.gov/pubmed/26740011
http://dx.doi.org/10.1038/srep18928
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author Lee, Gibok
Won, Hyung-Sik
Lee, Yoon-Mi
Choi, Jae-Wan
Oh, Taek-In
Jang, Jeong-Hwa
Choi, Dong-Kug
Lim, Beong-Ou
Kim, Young Jun
Park, Jong-Wan
Puigserver, Pere
Lim, Ji-Hong
author_facet Lee, Gibok
Won, Hyung-Sik
Lee, Yoon-Mi
Choi, Jae-Wan
Oh, Taek-In
Jang, Jeong-Hwa
Choi, Dong-Kug
Lim, Beong-Ou
Kim, Young Jun
Park, Jong-Wan
Puigserver, Pere
Lim, Ji-Hong
author_sort Lee, Gibok
collection PubMed
description Prolyl hydroxylase domain protein 2 (PHD2) belongs to an evolutionarily conserved superfamily of 2-oxoglutarate and Fe(II)-dependent dioxygenases that mediates homeostatic responses to oxygen deprivation by mediating hypoxia-inducible factor-1α (HIF-1α) hydroxylation and degradation. Although oxidative stress contributes to the inactivation of PHD2, the precise molecular mechanism of PHD2 inactivation independent of the levels of co-factors is not understood. Here, we identified disulfide bond-mediated PHD2 homo-dimer formation in response to oxidative stress caused by oxidizing agents and oncogenic H-ras(V12) signalling. Cysteine residues in the double-stranded β-helix fold that constitutes the catalytic site of PHD isoforms appeared responsible for the oxidative dimerization. Furthermore, we demonstrated that disulfide bond-mediated PHD2 dimerization is associated with the stabilization and activation of HIF-1α under oxidative stress. Oncogenic H-ras(V12) signalling facilitates the accumulation of HIF-1α in the nucleus and promotes aerobic glycolysis and lactate production. Moreover, oncogenic H-ras(V12) does not trigger aerobic glycolysis in antioxidant-treated or PHD2 knocked-down cells, suggesting the participation of the ROS-mediated PHD2 inactivation in the oncogenic H-ras(V12)-mediated metabolic reprogramming. We provide here a better understanding of the mechanism by which disulfide bond-mediated PHD2 dimerization and inactivation result in the activation of HIF-1α and aerobic glycolysis in response to oxidative stress.
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spelling pubmed-47039632016-01-19 Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation Lee, Gibok Won, Hyung-Sik Lee, Yoon-Mi Choi, Jae-Wan Oh, Taek-In Jang, Jeong-Hwa Choi, Dong-Kug Lim, Beong-Ou Kim, Young Jun Park, Jong-Wan Puigserver, Pere Lim, Ji-Hong Sci Rep Article Prolyl hydroxylase domain protein 2 (PHD2) belongs to an evolutionarily conserved superfamily of 2-oxoglutarate and Fe(II)-dependent dioxygenases that mediates homeostatic responses to oxygen deprivation by mediating hypoxia-inducible factor-1α (HIF-1α) hydroxylation and degradation. Although oxidative stress contributes to the inactivation of PHD2, the precise molecular mechanism of PHD2 inactivation independent of the levels of co-factors is not understood. Here, we identified disulfide bond-mediated PHD2 homo-dimer formation in response to oxidative stress caused by oxidizing agents and oncogenic H-ras(V12) signalling. Cysteine residues in the double-stranded β-helix fold that constitutes the catalytic site of PHD isoforms appeared responsible for the oxidative dimerization. Furthermore, we demonstrated that disulfide bond-mediated PHD2 dimerization is associated with the stabilization and activation of HIF-1α under oxidative stress. Oncogenic H-ras(V12) signalling facilitates the accumulation of HIF-1α in the nucleus and promotes aerobic glycolysis and lactate production. Moreover, oncogenic H-ras(V12) does not trigger aerobic glycolysis in antioxidant-treated or PHD2 knocked-down cells, suggesting the participation of the ROS-mediated PHD2 inactivation in the oncogenic H-ras(V12)-mediated metabolic reprogramming. We provide here a better understanding of the mechanism by which disulfide bond-mediated PHD2 dimerization and inactivation result in the activation of HIF-1α and aerobic glycolysis in response to oxidative stress. Nature Publishing Group 2016-01-07 /pmc/articles/PMC4703963/ /pubmed/26740011 http://dx.doi.org/10.1038/srep18928 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lee, Gibok
Won, Hyung-Sik
Lee, Yoon-Mi
Choi, Jae-Wan
Oh, Taek-In
Jang, Jeong-Hwa
Choi, Dong-Kug
Lim, Beong-Ou
Kim, Young Jun
Park, Jong-Wan
Puigserver, Pere
Lim, Ji-Hong
Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation
title Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation
title_full Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation
title_fullStr Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation
title_full_unstemmed Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation
title_short Oxidative Dimerization of PHD2 is Responsible for its Inactivation and Contributes to Metabolic Reprogramming via HIF-1α Activation
title_sort oxidative dimerization of phd2 is responsible for its inactivation and contributes to metabolic reprogramming via hif-1α activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4703963/
https://www.ncbi.nlm.nih.gov/pubmed/26740011
http://dx.doi.org/10.1038/srep18928
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