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Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae

Developmentally programmed formation of DNA double-strand breaks (DSBs) by Spo11 initiates a recombination mechanism that promotes synapsis and the subsequent segregation of homologous chromosomes during meiosis. Although DSBs are induced to high levels in meiosis, their formation and repair are tig...

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Detalles Bibliográficos
Autores principales: Yadav, Vikash Kumar, Claeys Bouuaert, Corentin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968521/
https://www.ncbi.nlm.nih.gov/pubmed/33748134
http://dx.doi.org/10.3389/fcell.2021.642737
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author Yadav, Vikash Kumar
Claeys Bouuaert, Corentin
author_facet Yadav, Vikash Kumar
Claeys Bouuaert, Corentin
author_sort Yadav, Vikash Kumar
collection PubMed
description Developmentally programmed formation of DNA double-strand breaks (DSBs) by Spo11 initiates a recombination mechanism that promotes synapsis and the subsequent segregation of homologous chromosomes during meiosis. Although DSBs are induced to high levels in meiosis, their formation and repair are tightly regulated to minimize potentially dangerous consequences for genomic integrity. In S. cerevisiae, nine proteins participate with Spo11 in DSB formation, but their molecular functions have been challenging to define. Here, we describe our current view of the mechanism of meiotic DSB formation based on recent advances in the characterization of the structure and function of DSB proteins and discuss regulatory pathways in the light of recent models.
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spelling pubmed-79685212021-03-18 Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae Yadav, Vikash Kumar Claeys Bouuaert, Corentin Front Cell Dev Biol Cell and Developmental Biology Developmentally programmed formation of DNA double-strand breaks (DSBs) by Spo11 initiates a recombination mechanism that promotes synapsis and the subsequent segregation of homologous chromosomes during meiosis. Although DSBs are induced to high levels in meiosis, their formation and repair are tightly regulated to minimize potentially dangerous consequences for genomic integrity. In S. cerevisiae, nine proteins participate with Spo11 in DSB formation, but their molecular functions have been challenging to define. Here, we describe our current view of the mechanism of meiotic DSB formation based on recent advances in the characterization of the structure and function of DSB proteins and discuss regulatory pathways in the light of recent models. Frontiers Media S.A. 2021-03-02 /pmc/articles/PMC7968521/ /pubmed/33748134 http://dx.doi.org/10.3389/fcell.2021.642737 Text en Copyright © 2021 Yadav and Claeys Bouuaert. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Yadav, Vikash Kumar
Claeys Bouuaert, Corentin
Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae
title Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae
title_full Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae
title_fullStr Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae
title_full_unstemmed Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae
title_short Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae
title_sort mechanism and control of meiotic dna double-strand break formation in s. cerevisiae
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968521/
https://www.ncbi.nlm.nih.gov/pubmed/33748134
http://dx.doi.org/10.3389/fcell.2021.642737
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