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Computational modelling of meiotic entry and commitment
In response to developmental and environmental conditions, cells exit the mitotic cell cycle and enter the meiosis program to generate haploid gametes from diploid germ cells. Once cells decide to enter the meiosis program they become irreversibly committed to the completion of meiosis irrespective...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760542/ https://www.ncbi.nlm.nih.gov/pubmed/29317645 http://dx.doi.org/10.1038/s41598-017-17478-9 |
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author | Bhola, Tanvi Kapuy, Orsolya Vinod, P. K. |
author_facet | Bhola, Tanvi Kapuy, Orsolya Vinod, P. K. |
author_sort | Bhola, Tanvi |
collection | PubMed |
description | In response to developmental and environmental conditions, cells exit the mitotic cell cycle and enter the meiosis program to generate haploid gametes from diploid germ cells. Once cells decide to enter the meiosis program they become irreversibly committed to the completion of meiosis irrespective of the presence of cue signals. How meiotic entry and commitment occur due to the dynamics of the regulatory network is not well understood. Therefore, we constructed a mathematical model of the regulatory network that controls the transition from mitosis to meiosis in Schizosaccharomyces pombe. Upon nitrogen starvation, yeast cells exit mitosis and undergo conjugation and meiotic entry. The model includes the regulation of Mei2, an RNA binding protein required for conjugation and meiotic entry, by multiple feedback loops involving Pat1, a kinase that keeps cells in mitosis, and Ste11, a transcription activator required for the sexual differentiation. The model accounts for various experimental observations and demonstrates that the activation of Mei2 is bistable, which ensures the irreversible commitment to meiosis. Further, we show by integrating the meiosis-specific regulation with a cell cycle model, the dynamics of cell cycle exit, G1 arrest and entry into meiosis under nitrogen starvation. |
format | Online Article Text |
id | pubmed-5760542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57605422018-01-17 Computational modelling of meiotic entry and commitment Bhola, Tanvi Kapuy, Orsolya Vinod, P. K. Sci Rep Article In response to developmental and environmental conditions, cells exit the mitotic cell cycle and enter the meiosis program to generate haploid gametes from diploid germ cells. Once cells decide to enter the meiosis program they become irreversibly committed to the completion of meiosis irrespective of the presence of cue signals. How meiotic entry and commitment occur due to the dynamics of the regulatory network is not well understood. Therefore, we constructed a mathematical model of the regulatory network that controls the transition from mitosis to meiosis in Schizosaccharomyces pombe. Upon nitrogen starvation, yeast cells exit mitosis and undergo conjugation and meiotic entry. The model includes the regulation of Mei2, an RNA binding protein required for conjugation and meiotic entry, by multiple feedback loops involving Pat1, a kinase that keeps cells in mitosis, and Ste11, a transcription activator required for the sexual differentiation. The model accounts for various experimental observations and demonstrates that the activation of Mei2 is bistable, which ensures the irreversible commitment to meiosis. Further, we show by integrating the meiosis-specific regulation with a cell cycle model, the dynamics of cell cycle exit, G1 arrest and entry into meiosis under nitrogen starvation. Nature Publishing Group UK 2018-01-09 /pmc/articles/PMC5760542/ /pubmed/29317645 http://dx.doi.org/10.1038/s41598-017-17478-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bhola, Tanvi Kapuy, Orsolya Vinod, P. K. Computational modelling of meiotic entry and commitment |
title | Computational modelling of meiotic entry and commitment |
title_full | Computational modelling of meiotic entry and commitment |
title_fullStr | Computational modelling of meiotic entry and commitment |
title_full_unstemmed | Computational modelling of meiotic entry and commitment |
title_short | Computational modelling of meiotic entry and commitment |
title_sort | computational modelling of meiotic entry and commitment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760542/ https://www.ncbi.nlm.nih.gov/pubmed/29317645 http://dx.doi.org/10.1038/s41598-017-17478-9 |
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