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Ubiquitination-dependent control of sexual differentiation in fission yeast

In fission yeast, meiosis-specific transcripts are selectively eliminated during vegetative growth by the combined action of the YTH-family RNA-binding protein Mmi1 and the nuclear exosome. Upon nutritional starvation, the master regulator of meiosis Mei2 inactivates Mmi1, thereby allowing expressio...

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Autores principales: Simonetti, Fabrizio, Candelli, Tito, Leon, Sebastien, Libri, Domenico, Rougemaille, Mathieu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614563/
https://www.ncbi.nlm.nih.gov/pubmed/28841135
http://dx.doi.org/10.7554/eLife.28046
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author Simonetti, Fabrizio
Candelli, Tito
Leon, Sebastien
Libri, Domenico
Rougemaille, Mathieu
author_facet Simonetti, Fabrizio
Candelli, Tito
Leon, Sebastien
Libri, Domenico
Rougemaille, Mathieu
author_sort Simonetti, Fabrizio
collection PubMed
description In fission yeast, meiosis-specific transcripts are selectively eliminated during vegetative growth by the combined action of the YTH-family RNA-binding protein Mmi1 and the nuclear exosome. Upon nutritional starvation, the master regulator of meiosis Mei2 inactivates Mmi1, thereby allowing expression of the meiotic program. Here, we show that the E3 ubiquitin ligase subunit Not4/Mot2 of the evolutionarily conserved Ccr4-Not complex, which associates with Mmi1, promotes suppression of meiotic transcripts expression in mitotic cells. Our analyses suggest that Mot2 directs ubiquitination of Mei2 to preserve the activity of Mmi1 during vegetative growth. Importantly, Mot2 is not involved in the constitutive pathway of Mei2 turnover, but rather plays a regulatory role to limit its accumulation or inhibit its function. We propose that Mmi1 recruits the Ccr4-Not complex to counteract its own inhibitor Mei2, thereby locking the system in a stable state that ensures the repression of the meiotic program by Mmi1.
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spelling pubmed-56145632017-09-28 Ubiquitination-dependent control of sexual differentiation in fission yeast Simonetti, Fabrizio Candelli, Tito Leon, Sebastien Libri, Domenico Rougemaille, Mathieu eLife Chromosomes and Gene Expression In fission yeast, meiosis-specific transcripts are selectively eliminated during vegetative growth by the combined action of the YTH-family RNA-binding protein Mmi1 and the nuclear exosome. Upon nutritional starvation, the master regulator of meiosis Mei2 inactivates Mmi1, thereby allowing expression of the meiotic program. Here, we show that the E3 ubiquitin ligase subunit Not4/Mot2 of the evolutionarily conserved Ccr4-Not complex, which associates with Mmi1, promotes suppression of meiotic transcripts expression in mitotic cells. Our analyses suggest that Mot2 directs ubiquitination of Mei2 to preserve the activity of Mmi1 during vegetative growth. Importantly, Mot2 is not involved in the constitutive pathway of Mei2 turnover, but rather plays a regulatory role to limit its accumulation or inhibit its function. We propose that Mmi1 recruits the Ccr4-Not complex to counteract its own inhibitor Mei2, thereby locking the system in a stable state that ensures the repression of the meiotic program by Mmi1. eLife Sciences Publications, Ltd 2017-08-25 /pmc/articles/PMC5614563/ /pubmed/28841135 http://dx.doi.org/10.7554/eLife.28046 Text en © 2017, Simonetti et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Chromosomes and Gene Expression
Simonetti, Fabrizio
Candelli, Tito
Leon, Sebastien
Libri, Domenico
Rougemaille, Mathieu
Ubiquitination-dependent control of sexual differentiation in fission yeast
title Ubiquitination-dependent control of sexual differentiation in fission yeast
title_full Ubiquitination-dependent control of sexual differentiation in fission yeast
title_fullStr Ubiquitination-dependent control of sexual differentiation in fission yeast
title_full_unstemmed Ubiquitination-dependent control of sexual differentiation in fission yeast
title_short Ubiquitination-dependent control of sexual differentiation in fission yeast
title_sort ubiquitination-dependent control of sexual differentiation in fission yeast
topic Chromosomes and Gene Expression
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614563/
https://www.ncbi.nlm.nih.gov/pubmed/28841135
http://dx.doi.org/10.7554/eLife.28046
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