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The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells
Changes in the location of γ-tubulin ensure cell survival and preserve genome integrity. We investigated whether the nuclear accumulation of γ-tubulin facilitates the transport of proliferating cell nuclear antigen (PCNA) between the cytosolic and the nuclear compartment in mammalian cells. We found...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219688/ https://www.ncbi.nlm.nih.gov/pubmed/34158617 http://dx.doi.org/10.1038/s42003-021-02280-1 |
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author | Corvaisier, Matthieu Zhou, Jingkai Malycheva, Darina Cornella, Nicola Chioureas, Dimitrios Gustafsson, Nina M. S. Rosselló, Catalina Ana Ayora, Silvia Li, Tongbin Ekström-Holka, Kristina Jirström, Karin Lindström, Lisa Alvarado-Kristensson, Maria |
author_facet | Corvaisier, Matthieu Zhou, Jingkai Malycheva, Darina Cornella, Nicola Chioureas, Dimitrios Gustafsson, Nina M. S. Rosselló, Catalina Ana Ayora, Silvia Li, Tongbin Ekström-Holka, Kristina Jirström, Karin Lindström, Lisa Alvarado-Kristensson, Maria |
author_sort | Corvaisier, Matthieu |
collection | PubMed |
description | Changes in the location of γ-tubulin ensure cell survival and preserve genome integrity. We investigated whether the nuclear accumulation of γ-tubulin facilitates the transport of proliferating cell nuclear antigen (PCNA) between the cytosolic and the nuclear compartment in mammalian cells. We found that the γ-tubulin meshwork assists in the recruitment of PCNA to chromatin. Also, decreased levels of γ-tubulin reduce the nuclear pool of PCNA. In addition, the γ-tubulin C terminus encodes a PCNA-interacting peptide (PIP) motif, and a γ-tubulin–PIP-mutant affects the nuclear accumulation of PCNA. In a cell-free system, PCNA and γ-tubulin formed a complex. In tumors, there is a significant positive correlation between TUBG1 and PCNA expression. Thus, we report a novel mechanism that constitutes the basis for tumor growth by which the γ-tubulin meshwork maintains indefinite proliferation by acting as an opportune scaffold for the transport of PCNA from the cytosol to the chromatin. |
format | Online Article Text |
id | pubmed-8219688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82196882021-07-09 The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells Corvaisier, Matthieu Zhou, Jingkai Malycheva, Darina Cornella, Nicola Chioureas, Dimitrios Gustafsson, Nina M. S. Rosselló, Catalina Ana Ayora, Silvia Li, Tongbin Ekström-Holka, Kristina Jirström, Karin Lindström, Lisa Alvarado-Kristensson, Maria Commun Biol Article Changes in the location of γ-tubulin ensure cell survival and preserve genome integrity. We investigated whether the nuclear accumulation of γ-tubulin facilitates the transport of proliferating cell nuclear antigen (PCNA) between the cytosolic and the nuclear compartment in mammalian cells. We found that the γ-tubulin meshwork assists in the recruitment of PCNA to chromatin. Also, decreased levels of γ-tubulin reduce the nuclear pool of PCNA. In addition, the γ-tubulin C terminus encodes a PCNA-interacting peptide (PIP) motif, and a γ-tubulin–PIP-mutant affects the nuclear accumulation of PCNA. In a cell-free system, PCNA and γ-tubulin formed a complex. In tumors, there is a significant positive correlation between TUBG1 and PCNA expression. Thus, we report a novel mechanism that constitutes the basis for tumor growth by which the γ-tubulin meshwork maintains indefinite proliferation by acting as an opportune scaffold for the transport of PCNA from the cytosol to the chromatin. Nature Publishing Group UK 2021-06-22 /pmc/articles/PMC8219688/ /pubmed/34158617 http://dx.doi.org/10.1038/s42003-021-02280-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Corvaisier, Matthieu Zhou, Jingkai Malycheva, Darina Cornella, Nicola Chioureas, Dimitrios Gustafsson, Nina M. S. Rosselló, Catalina Ana Ayora, Silvia Li, Tongbin Ekström-Holka, Kristina Jirström, Karin Lindström, Lisa Alvarado-Kristensson, Maria The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells |
title | The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells |
title_full | The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells |
title_fullStr | The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells |
title_full_unstemmed | The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells |
title_short | The γ-tubulin meshwork assists in the recruitment of PCNA to chromatin in mammalian cells |
title_sort | γ-tubulin meshwork assists in the recruitment of pcna to chromatin in mammalian cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219688/ https://www.ncbi.nlm.nih.gov/pubmed/34158617 http://dx.doi.org/10.1038/s42003-021-02280-1 |
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