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The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression
Hypoxia-inducible factors (HIFs) are key regulators of hypoxic responses, and their stability and transcriptional activity are controlled by several kinases. However, the regulation of HIF by protein phosphatases has not been thoroughly investigated. Here, we found that overexpression of Mg(2+)/Mn(2...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121667/ https://www.ncbi.nlm.nih.gov/pubmed/30081604 http://dx.doi.org/10.3390/ijms19082297 |
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author | Pyo, Jaehyuk Ryu, Jaewook Kim, Wootae Choi, Jae-Sun Jeong, Joo-Won Kim, Ja-Eun |
author_facet | Pyo, Jaehyuk Ryu, Jaewook Kim, Wootae Choi, Jae-Sun Jeong, Joo-Won Kim, Ja-Eun |
author_sort | Pyo, Jaehyuk |
collection | PubMed |
description | Hypoxia-inducible factors (HIFs) are key regulators of hypoxic responses, and their stability and transcriptional activity are controlled by several kinases. However, the regulation of HIF by protein phosphatases has not been thoroughly investigated. Here, we found that overexpression of Mg(2+)/Mn(2+)-dependent protein phosphatase 1 gamma (PPM1G), one of Ser/Thr protein phosphatases, downregulated protein expression of ectopic HIF-1α under normoxic or acute hypoxic conditions. In addition, the deficiency of PPM1G upregulated protein expression of endogenous HIF-1α under normoxic or acute oxidative stress conditions. PPM1G decreased expression of HIF-1α via the proteasomal pathway. PPM1G-mediated HIF-1α degradation was dependent on prolyl hydroxylase (PHD), but independent of von Hippel-Lindau (VHL). These data suggest that PPM1G is critical for the control of HIF-1α-dependent responses. |
format | Online Article Text |
id | pubmed-6121667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61216672018-09-07 The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression Pyo, Jaehyuk Ryu, Jaewook Kim, Wootae Choi, Jae-Sun Jeong, Joo-Won Kim, Ja-Eun Int J Mol Sci Article Hypoxia-inducible factors (HIFs) are key regulators of hypoxic responses, and their stability and transcriptional activity are controlled by several kinases. However, the regulation of HIF by protein phosphatases has not been thoroughly investigated. Here, we found that overexpression of Mg(2+)/Mn(2+)-dependent protein phosphatase 1 gamma (PPM1G), one of Ser/Thr protein phosphatases, downregulated protein expression of ectopic HIF-1α under normoxic or acute hypoxic conditions. In addition, the deficiency of PPM1G upregulated protein expression of endogenous HIF-1α under normoxic or acute oxidative stress conditions. PPM1G decreased expression of HIF-1α via the proteasomal pathway. PPM1G-mediated HIF-1α degradation was dependent on prolyl hydroxylase (PHD), but independent of von Hippel-Lindau (VHL). These data suggest that PPM1G is critical for the control of HIF-1α-dependent responses. MDPI 2018-08-05 /pmc/articles/PMC6121667/ /pubmed/30081604 http://dx.doi.org/10.3390/ijms19082297 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pyo, Jaehyuk Ryu, Jaewook Kim, Wootae Choi, Jae-Sun Jeong, Joo-Won Kim, Ja-Eun The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression |
title | The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression |
title_full | The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression |
title_fullStr | The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression |
title_full_unstemmed | The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression |
title_short | The Protein Phosphatase PPM1G Destabilizes HIF-1α Expression |
title_sort | protein phosphatase ppm1g destabilizes hif-1α expression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121667/ https://www.ncbi.nlm.nih.gov/pubmed/30081604 http://dx.doi.org/10.3390/ijms19082297 |
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