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Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors
The Saccharomyces cerevisiae centrosome or spindle pole body (SPB) is a dynamic structure that is remodeled in a cell cycle dependent manner. The SPB increases in size late in the cell cycle and during most cell cycle arrests and exchanges components during G1/S. We identified proteins involved in t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980476/ https://www.ncbi.nlm.nih.gov/pubmed/21103054 http://dx.doi.org/10.1371/journal.pone.0015426 |
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author | Greenland, Kristen B. Ding, Huiming Costanzo, Michael Boone, Charles Davis, Trisha N. |
author_facet | Greenland, Kristen B. Ding, Huiming Costanzo, Michael Boone, Charles Davis, Trisha N. |
author_sort | Greenland, Kristen B. |
collection | PubMed |
description | The Saccharomyces cerevisiae centrosome or spindle pole body (SPB) is a dynamic structure that is remodeled in a cell cycle dependent manner. The SPB increases in size late in the cell cycle and during most cell cycle arrests and exchanges components during G1/S. We identified proteins involved in the remodeling process using a strain in which SPB remodeling is conditionally induced. This strain was engineered to express a modified SPB component, Spc110, which can be cleaved upon the induction of a protease. Using a synthetic genetic array analysis, we screened for genes required only when Spc110 cleavage is induced. Candidate SPB remodeling factors fell into several functional categories: mitotic regulators, microtubule motors, protein modification enzymes, and nuclear pore proteins. The involvement of candidate genes in SPB assembly was assessed in three ways: by identifying the presence of a synthetic growth defect when combined with an Spc110 assembly defective mutant, quantifying growth of SPBs during metaphase arrest, and comparing distribution of SPB size during asynchronous growth. These secondary screens identified four genes required for SPB remodeling: NUP60, POM152, and NCS2 are required for SPB growth during a mitotic cell cycle arrest, and UBC4 is required to maintain SPB size during the cell cycle. These findings implicate the nuclear pore, urmylation, and ubiquitination in SPB remodeling and represent novel functions for these genes. |
format | Text |
id | pubmed-2980476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29804762010-11-22 Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors Greenland, Kristen B. Ding, Huiming Costanzo, Michael Boone, Charles Davis, Trisha N. PLoS One Research Article The Saccharomyces cerevisiae centrosome or spindle pole body (SPB) is a dynamic structure that is remodeled in a cell cycle dependent manner. The SPB increases in size late in the cell cycle and during most cell cycle arrests and exchanges components during G1/S. We identified proteins involved in the remodeling process using a strain in which SPB remodeling is conditionally induced. This strain was engineered to express a modified SPB component, Spc110, which can be cleaved upon the induction of a protease. Using a synthetic genetic array analysis, we screened for genes required only when Spc110 cleavage is induced. Candidate SPB remodeling factors fell into several functional categories: mitotic regulators, microtubule motors, protein modification enzymes, and nuclear pore proteins. The involvement of candidate genes in SPB assembly was assessed in three ways: by identifying the presence of a synthetic growth defect when combined with an Spc110 assembly defective mutant, quantifying growth of SPBs during metaphase arrest, and comparing distribution of SPB size during asynchronous growth. These secondary screens identified four genes required for SPB remodeling: NUP60, POM152, and NCS2 are required for SPB growth during a mitotic cell cycle arrest, and UBC4 is required to maintain SPB size during the cell cycle. These findings implicate the nuclear pore, urmylation, and ubiquitination in SPB remodeling and represent novel functions for these genes. Public Library of Science 2010-11-12 /pmc/articles/PMC2980476/ /pubmed/21103054 http://dx.doi.org/10.1371/journal.pone.0015426 Text en Greenland 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 Greenland, Kristen B. Ding, Huiming Costanzo, Michael Boone, Charles Davis, Trisha N. Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors |
title | Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors |
title_full | Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors |
title_fullStr | Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors |
title_full_unstemmed | Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors |
title_short | Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors |
title_sort | identification of saccharomyces cerevisiae spindle pole body remodeling factors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980476/ https://www.ncbi.nlm.nih.gov/pubmed/21103054 http://dx.doi.org/10.1371/journal.pone.0015426 |
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