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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...

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Autores principales: Gentili, Christian, Castor, Dennis, Kaden, Svenja, Lauterbach, David, Gysi, Mario, Steigemann, Patrick, Gerlich, Daniel W., Jiricny, Josef, Ferrari, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
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.
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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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