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TD-60 links RalA GTPase function to the CPC in mitosis
TD-60 (also known as RCC2) is a highly conserved protein that structurally resembles the Ran guanine exchange factor (GEF) RCC1, but has not previously been shown to have GEF activity. TD-60 has a typical chromosomal passenger complex (CPC) distribution in mitotic cells, but associates with integrin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510650/ https://www.ncbi.nlm.nih.gov/pubmed/26158537 http://dx.doi.org/10.1038/ncomms8678 |
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author | Papini, Diana Langemeyer, Lars Abad, Maria A. Kerr, Alastair Samejima, Itaru Eyers, Patrick A. Jeyaprakash, A. Arockia Higgins, Jonathan M. G. Barr, Francis A. Earnshaw, William C. |
author_facet | Papini, Diana Langemeyer, Lars Abad, Maria A. Kerr, Alastair Samejima, Itaru Eyers, Patrick A. Jeyaprakash, A. Arockia Higgins, Jonathan M. G. Barr, Francis A. Earnshaw, William C. |
author_sort | Papini, Diana |
collection | PubMed |
description | TD-60 (also known as RCC2) is a highly conserved protein that structurally resembles the Ran guanine exchange factor (GEF) RCC1, but has not previously been shown to have GEF activity. TD-60 has a typical chromosomal passenger complex (CPC) distribution in mitotic cells, but associates with integrin complexes and is involved in cell motility during interphase. Here we show that TD-60 exhibits GEF activity, in vitro and in cells, for the small GTPase RalA. TD-60 or RalA depletion causes spindle abnormalities in prometaphase associated with abnormal centromeric accumulation of CPC components. TD-60 and RalA apparently work together to contribute to the regulation of kinetochore–microtubule interactions in early mitosis. Importantly, several mitotic phenotypes caused by TD-60 depletion are reverted by the expression of a GTP-locked mutant, RalA (Q72L). The demonstration that a small GTPase participates in the regulation of the CPC reveals a level of mitotic regulation not suspected in previous studies. |
format | Online Article Text |
id | pubmed-4510650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45106502015-07-28 TD-60 links RalA GTPase function to the CPC in mitosis Papini, Diana Langemeyer, Lars Abad, Maria A. Kerr, Alastair Samejima, Itaru Eyers, Patrick A. Jeyaprakash, A. Arockia Higgins, Jonathan M. G. Barr, Francis A. Earnshaw, William C. Nat Commun Article TD-60 (also known as RCC2) is a highly conserved protein that structurally resembles the Ran guanine exchange factor (GEF) RCC1, but has not previously been shown to have GEF activity. TD-60 has a typical chromosomal passenger complex (CPC) distribution in mitotic cells, but associates with integrin complexes and is involved in cell motility during interphase. Here we show that TD-60 exhibits GEF activity, in vitro and in cells, for the small GTPase RalA. TD-60 or RalA depletion causes spindle abnormalities in prometaphase associated with abnormal centromeric accumulation of CPC components. TD-60 and RalA apparently work together to contribute to the regulation of kinetochore–microtubule interactions in early mitosis. Importantly, several mitotic phenotypes caused by TD-60 depletion are reverted by the expression of a GTP-locked mutant, RalA (Q72L). The demonstration that a small GTPase participates in the regulation of the CPC reveals a level of mitotic regulation not suspected in previous studies. Nature Pub. Group 2015-07-09 /pmc/articles/PMC4510650/ /pubmed/26158537 http://dx.doi.org/10.1038/ncomms8678 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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 Papini, Diana Langemeyer, Lars Abad, Maria A. Kerr, Alastair Samejima, Itaru Eyers, Patrick A. Jeyaprakash, A. Arockia Higgins, Jonathan M. G. Barr, Francis A. Earnshaw, William C. TD-60 links RalA GTPase function to the CPC in mitosis |
title | TD-60 links RalA GTPase function to the CPC in mitosis |
title_full | TD-60 links RalA GTPase function to the CPC in mitosis |
title_fullStr | TD-60 links RalA GTPase function to the CPC in mitosis |
title_full_unstemmed | TD-60 links RalA GTPase function to the CPC in mitosis |
title_short | TD-60 links RalA GTPase function to the CPC in mitosis |
title_sort | td-60 links rala gtpase function to the cpc in mitosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510650/ https://www.ncbi.nlm.nih.gov/pubmed/26158537 http://dx.doi.org/10.1038/ncomms8678 |
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