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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...

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Autores principales: Seitz, Brian C., Mucelli, Xheni, Majano, Maira, Wallis, Zoey, Dodge, Ashley C., Carmona, Catherine, Durant, Matthew, Maynard, Sharra, Huang, Linda S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2023
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.
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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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