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The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast

Quiescence and gametogenesis represent two distinct survival strategies in response to nutrient starvation in budding yeast. Precisely how environmental signals are sensed by yeast cells to trigger quiescence and gametogenesis is not fully understood. A conserved signalling module consisting of Grea...

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Autores principales: Sarkar, Sourav, Dalgaard, Jacob Z., Millar, Jonathan B. A., Arumugam, Prakash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072559/
https://www.ncbi.nlm.nih.gov/pubmed/24968058
http://dx.doi.org/10.1371/journal.pgen.1004456
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author Sarkar, Sourav
Dalgaard, Jacob Z.
Millar, Jonathan B. A.
Arumugam, Prakash
author_facet Sarkar, Sourav
Dalgaard, Jacob Z.
Millar, Jonathan B. A.
Arumugam, Prakash
author_sort Sarkar, Sourav
collection PubMed
description Quiescence and gametogenesis represent two distinct survival strategies in response to nutrient starvation in budding yeast. Precisely how environmental signals are sensed by yeast cells to trigger quiescence and gametogenesis is not fully understood. A conserved signalling module consisting of Greatwall kinase, Endosulfine and Protein Phosphatase PP2A(Cdc55) proteins regulates entry into mitosis in Xenopus egg extracts and meiotic maturation in flies. We report here that an analogous signalling module consisting of the serine-threonine kinase Rim15, the Endosulfines Igo1 and Igo2 and the Protein Phosphatase PP2A(Cdc55), regulates entry into both quiescence and gametogenesis in budding yeast. PP2A(Cdc55) inhibits entry into gametogenesis and quiescence. Rim15 promotes entry into gametogenesis and quiescence by converting Igo1 into an inhibitor of PP2A(Cdc55) by phosphorylating at a conserved serine residue. Moreover, we show that the Rim15-Endosulfine-PP2A(Cdc55) pathway regulates entry into quiescence and gametogenesis by distinct mechanisms. In addition, we show that Igo1 and Igo2 are required for pre-meiotic autophagy but the lack of pre-meiotic autophagy is insufficient to explain the sporulation defect of igo1Δ igo2Δ cells. We propose that the Rim15-Endosulfine-PP2A(Cdc55) signalling module triggers entry into quiescence and gametogenesis by regulating dephosphorylation of distinct substrates.
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spelling pubmed-40725592014-07-02 The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast Sarkar, Sourav Dalgaard, Jacob Z. Millar, Jonathan B. A. Arumugam, Prakash PLoS Genet Research Article Quiescence and gametogenesis represent two distinct survival strategies in response to nutrient starvation in budding yeast. Precisely how environmental signals are sensed by yeast cells to trigger quiescence and gametogenesis is not fully understood. A conserved signalling module consisting of Greatwall kinase, Endosulfine and Protein Phosphatase PP2A(Cdc55) proteins regulates entry into mitosis in Xenopus egg extracts and meiotic maturation in flies. We report here that an analogous signalling module consisting of the serine-threonine kinase Rim15, the Endosulfines Igo1 and Igo2 and the Protein Phosphatase PP2A(Cdc55), regulates entry into both quiescence and gametogenesis in budding yeast. PP2A(Cdc55) inhibits entry into gametogenesis and quiescence. Rim15 promotes entry into gametogenesis and quiescence by converting Igo1 into an inhibitor of PP2A(Cdc55) by phosphorylating at a conserved serine residue. Moreover, we show that the Rim15-Endosulfine-PP2A(Cdc55) pathway regulates entry into quiescence and gametogenesis by distinct mechanisms. In addition, we show that Igo1 and Igo2 are required for pre-meiotic autophagy but the lack of pre-meiotic autophagy is insufficient to explain the sporulation defect of igo1Δ igo2Δ cells. We propose that the Rim15-Endosulfine-PP2A(Cdc55) signalling module triggers entry into quiescence and gametogenesis by regulating dephosphorylation of distinct substrates. Public Library of Science 2014-06-26 /pmc/articles/PMC4072559/ /pubmed/24968058 http://dx.doi.org/10.1371/journal.pgen.1004456 Text en © 2014 Sarkar 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
Sarkar, Sourav
Dalgaard, Jacob Z.
Millar, Jonathan B. A.
Arumugam, Prakash
The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast
title The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast
title_full The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast
title_fullStr The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast
title_full_unstemmed The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast
title_short The Rim15-Endosulfine-PP2A(Cdc55) Signalling Module Regulates Entry into Gametogenesis and Quiescence via Distinct Mechanisms in Budding Yeast
title_sort rim15-endosulfine-pp2a(cdc55) signalling module regulates entry into gametogenesis and quiescence via distinct mechanisms in budding yeast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072559/
https://www.ncbi.nlm.nih.gov/pubmed/24968058
http://dx.doi.org/10.1371/journal.pgen.1004456
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