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PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function
PP2A(Cdc55) is a highly conserved serine-threonine protein phosphatase that is involved in diverse cellular processes. In budding yeast, meiotic cells lacking PP2A(Cdc55) activity undergo a premature exit from meiosis I which results in a failure to form bipolar spindles and divide nuclei. This defe...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960654/ https://www.ncbi.nlm.nih.gov/pubmed/27455870 http://dx.doi.org/10.1038/srep30397 |
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author | Kerr, Gary W. Wong, Jin Huei Arumugam, Prakash |
author_facet | Kerr, Gary W. Wong, Jin Huei Arumugam, Prakash |
author_sort | Kerr, Gary W. |
collection | PubMed |
description | PP2A(Cdc55) is a highly conserved serine-threonine protein phosphatase that is involved in diverse cellular processes. In budding yeast, meiotic cells lacking PP2A(Cdc55) activity undergo a premature exit from meiosis I which results in a failure to form bipolar spindles and divide nuclei. This defect is largely due to its role in negatively regulating the Cdc Fourteen Early Anaphase Release (FEAR) pathway. PP2A(Cdc55) prevents nucleolar release of the Cdk (Cyclin-dependent kinase)-antagonising phosphatase Cdc14 by counteracting phosphorylation of the nucleolar protein Net1 by Cdk. CDC55 was identified in a genetic screen for monopolins performed by isolating suppressors of spo11Δ spo12Δ lethality suggesting that Cdc55 might have a role in meiotic chromosome segregation. We investigated this possibility by isolating cdc55 alleles that suppress spo11Δ spo12Δ lethality and show that this suppression is independent of PP2A(Cdc55)’s FEAR function. Although the suppressor mutations in cdc55 affect reductional chromosome segregation in the absence of recombination, they have no effect on chromosome segregation during wild type meiosis. We suggest that Cdc55 is required for reductional chromosome segregation during achiasmate meiosis and this is independent of its FEAR function. |
format | Online Article Text |
id | pubmed-4960654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49606542016-08-05 PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function Kerr, Gary W. Wong, Jin Huei Arumugam, Prakash Sci Rep Article PP2A(Cdc55) is a highly conserved serine-threonine protein phosphatase that is involved in diverse cellular processes. In budding yeast, meiotic cells lacking PP2A(Cdc55) activity undergo a premature exit from meiosis I which results in a failure to form bipolar spindles and divide nuclei. This defect is largely due to its role in negatively regulating the Cdc Fourteen Early Anaphase Release (FEAR) pathway. PP2A(Cdc55) prevents nucleolar release of the Cdk (Cyclin-dependent kinase)-antagonising phosphatase Cdc14 by counteracting phosphorylation of the nucleolar protein Net1 by Cdk. CDC55 was identified in a genetic screen for monopolins performed by isolating suppressors of spo11Δ spo12Δ lethality suggesting that Cdc55 might have a role in meiotic chromosome segregation. We investigated this possibility by isolating cdc55 alleles that suppress spo11Δ spo12Δ lethality and show that this suppression is independent of PP2A(Cdc55)’s FEAR function. Although the suppressor mutations in cdc55 affect reductional chromosome segregation in the absence of recombination, they have no effect on chromosome segregation during wild type meiosis. We suggest that Cdc55 is required for reductional chromosome segregation during achiasmate meiosis and this is independent of its FEAR function. Nature Publishing Group 2016-07-26 /pmc/articles/PMC4960654/ /pubmed/27455870 http://dx.doi.org/10.1038/srep30397 Text en Copyright © 2016, The Author(s) 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 Kerr, Gary W. Wong, Jin Huei Arumugam, Prakash PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function |
title | PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function |
title_full | PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function |
title_fullStr | PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function |
title_full_unstemmed | PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function |
title_short | PP2A(Cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its FEAR function |
title_sort | pp2a(cdc55)’s role in reductional chromosome segregation during achiasmate meiosis in budding yeast is independent of its fear function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960654/ https://www.ncbi.nlm.nih.gov/pubmed/27455870 http://dx.doi.org/10.1038/srep30397 |
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