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Meiosis II spindle disassembly requires two distinct pathways
During exit from meiosis II, cells undergo several structural rearrangements, including disassembly of the meiosis II spindles and cytokinesis. Each of these changes is regulated to ensure that they occur at the proper time. Previous studies have demonstrated that both SPS1, which encodes a STE20-fa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551701/ https://www.ncbi.nlm.nih.gov/pubmed/37436806 http://dx.doi.org/10.1091/mbc.E23-03-0096 |
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author | Seitz, Brian C. Mucelli, Xheni Majano, Maira Wallis, Zoey Dodge, Ashley C. Carmona, Catherine Durant, Matthew Maynard, Sharra Huang, Linda S. |
author_facet | Seitz, Brian C. Mucelli, Xheni Majano, Maira Wallis, Zoey Dodge, Ashley C. Carmona, Catherine Durant, Matthew Maynard, Sharra Huang, Linda S. |
author_sort | Seitz, Brian C. |
collection | PubMed |
description | During exit from meiosis II, cells undergo several structural rearrangements, including disassembly of the meiosis II spindles and cytokinesis. Each of these changes is regulated to ensure that they occur at the proper time. Previous studies have demonstrated that both SPS1, which encodes a STE20-family GCKIII kinase, and AMA1, which encodes a meiosis-specific activator of the Anaphase Promoting Complex, are required for both meiosis II spindle disassembly and cytokinesis in the budding yeast Saccharomyces cerevisiae. We examine the relationship between meiosis II spindle disassembly and cytokinesis and find that the meiosis II spindle disassembly failure in sps1Δ and ama1∆ cells is not the cause of the cytokinesis defect. We also see that the spindle disassembly defects in sps1Δ and ama1∆ cells are phenotypically distinct. We examined known microtubule-associated proteins Ase1, Cin8, and Bim1, and found that AMA1 is required for the proper loss of Ase1 and Cin8 on meiosis II spindles while SPS1 is required for Bim1 loss in meiosis II. Taken together, these data indicate that SPS1 and AMA1 promote distinct aspects of meiosis II spindle disassembly, and that both pathways are required for the successful completion of meiosis. |
format | Online Article Text |
id | pubmed-10551701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-105517012023-11-01 Meiosis II spindle disassembly requires two distinct pathways Seitz, Brian C. Mucelli, Xheni Majano, Maira Wallis, Zoey Dodge, Ashley C. Carmona, Catherine Durant, Matthew Maynard, Sharra Huang, Linda S. Mol Biol Cell Articles During exit from meiosis II, cells undergo several structural rearrangements, including disassembly of the meiosis II spindles and cytokinesis. Each of these changes is regulated to ensure that they occur at the proper time. Previous studies have demonstrated that both SPS1, which encodes a STE20-family GCKIII kinase, and AMA1, which encodes a meiosis-specific activator of the Anaphase Promoting Complex, are required for both meiosis II spindle disassembly and cytokinesis in the budding yeast Saccharomyces cerevisiae. We examine the relationship between meiosis II spindle disassembly and cytokinesis and find that the meiosis II spindle disassembly failure in sps1Δ and ama1∆ cells is not the cause of the cytokinesis defect. We also see that the spindle disassembly defects in sps1Δ and ama1∆ cells are phenotypically distinct. We examined known microtubule-associated proteins Ase1, Cin8, and Bim1, and found that AMA1 is required for the proper loss of Ase1 and Cin8 on meiosis II spindles while SPS1 is required for Bim1 loss in meiosis II. Taken together, these data indicate that SPS1 and AMA1 promote distinct aspects of meiosis II spindle disassembly, and that both pathways are required for the successful completion of meiosis. The American Society for Cell Biology 2023-08-17 /pmc/articles/PMC10551701/ /pubmed/37436806 http://dx.doi.org/10.1091/mbc.E23-03-0096 Text en © 2023 Seitz, Mucelli, et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License. |
spellingShingle | Articles Seitz, Brian C. Mucelli, Xheni Majano, Maira Wallis, Zoey Dodge, Ashley C. Carmona, Catherine Durant, Matthew Maynard, Sharra Huang, Linda S. Meiosis II spindle disassembly requires two distinct pathways |
title | Meiosis II spindle disassembly requires two distinct pathways |
title_full | Meiosis II spindle disassembly requires two distinct pathways |
title_fullStr | Meiosis II spindle disassembly requires two distinct pathways |
title_full_unstemmed | Meiosis II spindle disassembly requires two distinct pathways |
title_short | Meiosis II spindle disassembly requires two distinct pathways |
title_sort | meiosis ii spindle disassembly requires two distinct pathways |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551701/ https://www.ncbi.nlm.nih.gov/pubmed/37436806 http://dx.doi.org/10.1091/mbc.E23-03-0096 |
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