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The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation
Folate metabolism is central to cell proliferation and a target of commonly used cancer chemotherapeutics. In particular, the mitochondrial folate-coupled metabolism is thought to be important for proliferating cancer cells. The enzyme MTHFD2 in this pathway is highly expressed in human tumors and b...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602236/ https://www.ncbi.nlm.nih.gov/pubmed/26461067 http://dx.doi.org/10.1038/srep15029 |
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author | Gustafsson Sheppard, Nina Jarl, Lisa Mahadessian, Diana Strittmatter, Laura Schmidt, Angelika Madhusudan, Nikhil Tegnér, Jesper Lundberg, Emma K. Asplund, Anna Jain, Mohit Nilsson, Roland |
author_facet | Gustafsson Sheppard, Nina Jarl, Lisa Mahadessian, Diana Strittmatter, Laura Schmidt, Angelika Madhusudan, Nikhil Tegnér, Jesper Lundberg, Emma K. Asplund, Anna Jain, Mohit Nilsson, Roland |
author_sort | Gustafsson Sheppard, Nina |
collection | PubMed |
description | Folate metabolism is central to cell proliferation and a target of commonly used cancer chemotherapeutics. In particular, the mitochondrial folate-coupled metabolism is thought to be important for proliferating cancer cells. The enzyme MTHFD2 in this pathway is highly expressed in human tumors and broadly required for survival of cancer cells. Although the enzymatic activity of the MTHFD2 protein is well understood, little is known about its larger role in cancer cell biology. We here report that MTHFD2 is co-expressed with two distinct gene sets, representing amino acid metabolism and cell proliferation, respectively. Consistent with a role for MTHFD2 in cell proliferation, MTHFD2 expression was repressed in cells rendered quiescent by deprivation of growth signals (serum) and rapidly re-induced by serum stimulation. Overexpression of MTHFD2 alone was sufficient to promote cell proliferation independent of its dehydrogenase activity, even during growth restriction. In addition to its known mitochondrial localization, we found MTHFD2 to have a nuclear localization and co-localize with DNA replication sites. These findings suggest a previously unknown role for MTHFD2 in cancer cell proliferation, adding to its known function in mitochondrial folate metabolism. |
format | Online Article Text |
id | pubmed-4602236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46022362015-10-23 The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation Gustafsson Sheppard, Nina Jarl, Lisa Mahadessian, Diana Strittmatter, Laura Schmidt, Angelika Madhusudan, Nikhil Tegnér, Jesper Lundberg, Emma K. Asplund, Anna Jain, Mohit Nilsson, Roland Sci Rep Article Folate metabolism is central to cell proliferation and a target of commonly used cancer chemotherapeutics. In particular, the mitochondrial folate-coupled metabolism is thought to be important for proliferating cancer cells. The enzyme MTHFD2 in this pathway is highly expressed in human tumors and broadly required for survival of cancer cells. Although the enzymatic activity of the MTHFD2 protein is well understood, little is known about its larger role in cancer cell biology. We here report that MTHFD2 is co-expressed with two distinct gene sets, representing amino acid metabolism and cell proliferation, respectively. Consistent with a role for MTHFD2 in cell proliferation, MTHFD2 expression was repressed in cells rendered quiescent by deprivation of growth signals (serum) and rapidly re-induced by serum stimulation. Overexpression of MTHFD2 alone was sufficient to promote cell proliferation independent of its dehydrogenase activity, even during growth restriction. In addition to its known mitochondrial localization, we found MTHFD2 to have a nuclear localization and co-localize with DNA replication sites. These findings suggest a previously unknown role for MTHFD2 in cancer cell proliferation, adding to its known function in mitochondrial folate metabolism. Nature Publishing Group 2015-10-13 /pmc/articles/PMC4602236/ /pubmed/26461067 http://dx.doi.org/10.1038/srep15029 Text en Copyright © 2015, 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 Gustafsson Sheppard, Nina Jarl, Lisa Mahadessian, Diana Strittmatter, Laura Schmidt, Angelika Madhusudan, Nikhil Tegnér, Jesper Lundberg, Emma K. Asplund, Anna Jain, Mohit Nilsson, Roland The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation |
title | The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation |
title_full | The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation |
title_fullStr | The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation |
title_full_unstemmed | The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation |
title_short | The folate-coupled enzyme MTHFD2 is a nuclear protein and promotes cell proliferation |
title_sort | folate-coupled enzyme mthfd2 is a nuclear protein and promotes cell proliferation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602236/ https://www.ncbi.nlm.nih.gov/pubmed/26461067 http://dx.doi.org/10.1038/srep15029 |
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