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Chromosome Missegregation Associated with RUVBL1 Deficiency
RUVBL1 (RuvB-like1) and RUVBL2 (RuvB-like 2) are integral components of multisubunit protein complexes involved in processes ranging from cellular metabolism, transcription and chromatin remodeling to DNA repair. Here, we show that although RUVBL1 and RUVBL2 are known to form heterodimeric complexes...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511761/ https://www.ncbi.nlm.nih.gov/pubmed/26201077 http://dx.doi.org/10.1371/journal.pone.0133576 |
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author | Gentili, Christian Castor, Dennis Kaden, Svenja Lauterbach, David Gysi, Mario Steigemann, Patrick Gerlich, Daniel W. Jiricny, Josef Ferrari, Stefano |
author_facet | Gentili, Christian Castor, Dennis Kaden, Svenja Lauterbach, David Gysi, Mario Steigemann, Patrick Gerlich, Daniel W. Jiricny, Josef Ferrari, Stefano |
author_sort | Gentili, Christian |
collection | PubMed |
description | RUVBL1 (RuvB-like1) and RUVBL2 (RuvB-like 2) are integral components of multisubunit protein complexes involved in processes ranging from cellular metabolism, transcription and chromatin remodeling to DNA repair. Here, we show that although RUVBL1 and RUVBL2 are known to form heterodimeric complexes in which they stabilize each other, the subunits separate during cytokinesis. In anaphase-to-telophase transition, RUVBL1 localizes to structures of the mitotic spindle apparatus, where it partially co-localizes with polo-like kinase 1 (PLK1). The ability of PLK1 to phosphorylate RUVBL1—but not RUVBL2—in vitro and their physical association in vivo suggest that this kinase differentially regulates the function of the RuvB-like proteins during mitosis. We further show that siRNA-mediated knock-down of RuvB-like proteins causes severe defects in chromosome alignment and segregation. In addition, we show that the ATPase activity of RUVBL1 is indispensable for cell proliferation. Our data thus demonstrate that RUVBL1 is essential for efficient mitosis and proliferation. |
format | Online Article Text |
id | pubmed-4511761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45117612015-07-24 Chromosome Missegregation Associated with RUVBL1 Deficiency Gentili, Christian Castor, Dennis Kaden, Svenja Lauterbach, David Gysi, Mario Steigemann, Patrick Gerlich, Daniel W. Jiricny, Josef Ferrari, Stefano PLoS One Research Article RUVBL1 (RuvB-like1) and RUVBL2 (RuvB-like 2) are integral components of multisubunit protein complexes involved in processes ranging from cellular metabolism, transcription and chromatin remodeling to DNA repair. Here, we show that although RUVBL1 and RUVBL2 are known to form heterodimeric complexes in which they stabilize each other, the subunits separate during cytokinesis. In anaphase-to-telophase transition, RUVBL1 localizes to structures of the mitotic spindle apparatus, where it partially co-localizes with polo-like kinase 1 (PLK1). The ability of PLK1 to phosphorylate RUVBL1—but not RUVBL2—in vitro and their physical association in vivo suggest that this kinase differentially regulates the function of the RuvB-like proteins during mitosis. We further show that siRNA-mediated knock-down of RuvB-like proteins causes severe defects in chromosome alignment and segregation. In addition, we show that the ATPase activity of RUVBL1 is indispensable for cell proliferation. Our data thus demonstrate that RUVBL1 is essential for efficient mitosis and proliferation. Public Library of Science 2015-07-22 /pmc/articles/PMC4511761/ /pubmed/26201077 http://dx.doi.org/10.1371/journal.pone.0133576 Text en © 2015 Gentili et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Gentili, Christian Castor, Dennis Kaden, Svenja Lauterbach, David Gysi, Mario Steigemann, Patrick Gerlich, Daniel W. Jiricny, Josef Ferrari, Stefano Chromosome Missegregation Associated with RUVBL1 Deficiency |
title | Chromosome Missegregation Associated with RUVBL1 Deficiency |
title_full | Chromosome Missegregation Associated with RUVBL1 Deficiency |
title_fullStr | Chromosome Missegregation Associated with RUVBL1 Deficiency |
title_full_unstemmed | Chromosome Missegregation Associated with RUVBL1 Deficiency |
title_short | Chromosome Missegregation Associated with RUVBL1 Deficiency |
title_sort | chromosome missegregation associated with ruvbl1 deficiency |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511761/ https://www.ncbi.nlm.nih.gov/pubmed/26201077 http://dx.doi.org/10.1371/journal.pone.0133576 |
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