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Parkin Regulates the Activity of Pyruvate Kinase M2
Parkin, a ubiquitin E3 ligase, is mutated in most cases of autosomal recessive early onset Parkinson disease. It was discovered that Parkin is also mutated in glioblastoma and other human malignancies and that it inhibits tumor cell growth. Here, we identified pyruvate kinase M2 (PKM2) as a unique s...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858978/ https://www.ncbi.nlm.nih.gov/pubmed/26975375 http://dx.doi.org/10.1074/jbc.M115.703066 |
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author | Liu, Kun Li, Fanzhou Han, Haichao Chen, Yue Mao, Zebin Luo, Jianyuan Zhao, Yingming Zheng, Bin Gu, Wei Zhao, Wenhui |
author_facet | Liu, Kun Li, Fanzhou Han, Haichao Chen, Yue Mao, Zebin Luo, Jianyuan Zhao, Yingming Zheng, Bin Gu, Wei Zhao, Wenhui |
author_sort | Liu, Kun |
collection | PubMed |
description | Parkin, a ubiquitin E3 ligase, is mutated in most cases of autosomal recessive early onset Parkinson disease. It was discovered that Parkin is also mutated in glioblastoma and other human malignancies and that it inhibits tumor cell growth. Here, we identified pyruvate kinase M2 (PKM2) as a unique substrate for parkin through biochemical purification. We found that parkin interacts with PKM2 both in vitro and in vivo, and this interaction dramatically increases during glucose starvation. Ubiquitylation of PKM2 by parkin does not affect its stability but decreases its enzymatic activity. Parkin regulates the glycolysis pathway and affects the cell metabolism. Our studies revealed the novel important roles of parkin in tumor cell metabolism and provided new insight for therapy of Parkinson disease. |
format | Online Article Text |
id | pubmed-4858978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-48589782016-05-12 Parkin Regulates the Activity of Pyruvate Kinase M2 Liu, Kun Li, Fanzhou Han, Haichao Chen, Yue Mao, Zebin Luo, Jianyuan Zhao, Yingming Zheng, Bin Gu, Wei Zhao, Wenhui J Biol Chem Signal Transduction Parkin, a ubiquitin E3 ligase, is mutated in most cases of autosomal recessive early onset Parkinson disease. It was discovered that Parkin is also mutated in glioblastoma and other human malignancies and that it inhibits tumor cell growth. Here, we identified pyruvate kinase M2 (PKM2) as a unique substrate for parkin through biochemical purification. We found that parkin interacts with PKM2 both in vitro and in vivo, and this interaction dramatically increases during glucose starvation. Ubiquitylation of PKM2 by parkin does not affect its stability but decreases its enzymatic activity. Parkin regulates the glycolysis pathway and affects the cell metabolism. Our studies revealed the novel important roles of parkin in tumor cell metabolism and provided new insight for therapy of Parkinson disease. American Society for Biochemistry and Molecular Biology 2016-05-06 2016-03-14 /pmc/articles/PMC4858978/ /pubmed/26975375 http://dx.doi.org/10.1074/jbc.M115.703066 Text en © 2016 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version free via Creative Commons CC-BY license (http://creativecommons.org/licenses/by/4.0) . |
spellingShingle | Signal Transduction Liu, Kun Li, Fanzhou Han, Haichao Chen, Yue Mao, Zebin Luo, Jianyuan Zhao, Yingming Zheng, Bin Gu, Wei Zhao, Wenhui Parkin Regulates the Activity of Pyruvate Kinase M2 |
title | Parkin Regulates the Activity of Pyruvate Kinase M2 |
title_full | Parkin Regulates the Activity of Pyruvate Kinase M2 |
title_fullStr | Parkin Regulates the Activity of Pyruvate Kinase M2 |
title_full_unstemmed | Parkin Regulates the Activity of Pyruvate Kinase M2 |
title_short | Parkin Regulates the Activity of Pyruvate Kinase M2 |
title_sort | parkin regulates the activity of pyruvate kinase m2 |
topic | Signal Transduction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858978/ https://www.ncbi.nlm.nih.gov/pubmed/26975375 http://dx.doi.org/10.1074/jbc.M115.703066 |
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