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The formation and repair of DNA double-strand breaks in mammalian meiosis

Programmed DNA double-strand breaks (DSBs) are necessary for meiosis in mammals. A sufficient number of DSBs ensure the normal pairing/synapsis of homologous chromosomes. Abnormal DSB repair undermines meiosis, leading to sterility in mammals. The DSBs that initiate recombination are repaired as cro...

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Autores principales: Qu, Wei, Liu, Cong, Xu, Ya-Ting, Xu, Yu-Min, Luo, Meng-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577251/
https://www.ncbi.nlm.nih.gov/pubmed/34708719
http://dx.doi.org/10.4103/aja202191
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author Qu, Wei
Liu, Cong
Xu, Ya-Ting
Xu, Yu-Min
Luo, Meng-Cheng
author_facet Qu, Wei
Liu, Cong
Xu, Ya-Ting
Xu, Yu-Min
Luo, Meng-Cheng
author_sort Qu, Wei
collection PubMed
description Programmed DNA double-strand breaks (DSBs) are necessary for meiosis in mammals. A sufficient number of DSBs ensure the normal pairing/synapsis of homologous chromosomes. Abnormal DSB repair undermines meiosis, leading to sterility in mammals. The DSBs that initiate recombination are repaired as crossovers and noncrossovers, and crossovers are required for correct chromosome separation. Thus, the placement, timing, and frequency of crossover formation must be tightly controlled. Importantly, mutations in many genes related to the formation and repair of DSB result in infertility in humans. These mutations cause nonobstructive azoospermia in men, premature ovarian insufficiency and ovarian dysgenesis in women. Here, we have illustrated the formation and repair of DSB in mammals, summarized major factors influencing the formation of DSB and the theories of crossover regulation.
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spelling pubmed-85772512021-11-10 The formation and repair of DNA double-strand breaks in mammalian meiosis Qu, Wei Liu, Cong Xu, Ya-Ting Xu, Yu-Min Luo, Meng-Cheng Asian J Androl Invited Review Programmed DNA double-strand breaks (DSBs) are necessary for meiosis in mammals. A sufficient number of DSBs ensure the normal pairing/synapsis of homologous chromosomes. Abnormal DSB repair undermines meiosis, leading to sterility in mammals. The DSBs that initiate recombination are repaired as crossovers and noncrossovers, and crossovers are required for correct chromosome separation. Thus, the placement, timing, and frequency of crossover formation must be tightly controlled. Importantly, mutations in many genes related to the formation and repair of DSB result in infertility in humans. These mutations cause nonobstructive azoospermia in men, premature ovarian insufficiency and ovarian dysgenesis in women. Here, we have illustrated the formation and repair of DSB in mammals, summarized major factors influencing the formation of DSB and the theories of crossover regulation. Wolters Kluwer - Medknow 2021-10-22 /pmc/articles/PMC8577251/ /pubmed/34708719 http://dx.doi.org/10.4103/aja202191 Text en Copyright: © The Author(s)(2021) https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Invited Review
Qu, Wei
Liu, Cong
Xu, Ya-Ting
Xu, Yu-Min
Luo, Meng-Cheng
The formation and repair of DNA double-strand breaks in mammalian meiosis
title The formation and repair of DNA double-strand breaks in mammalian meiosis
title_full The formation and repair of DNA double-strand breaks in mammalian meiosis
title_fullStr The formation and repair of DNA double-strand breaks in mammalian meiosis
title_full_unstemmed The formation and repair of DNA double-strand breaks in mammalian meiosis
title_short The formation and repair of DNA double-strand breaks in mammalian meiosis
title_sort formation and repair of dna double-strand breaks in mammalian meiosis
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577251/
https://www.ncbi.nlm.nih.gov/pubmed/34708719
http://dx.doi.org/10.4103/aja202191
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