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MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis
Repair of DNA double-strand breaks (DSBs) with homologous chromosomes is a hallmark of meiosis that is mediated by recombination ‘bridges’ between homolog axes. This process requires cooperation of DMC1 and RAD51 to promote homology search and strand exchange. The mechanism(s) regulating DMC1/RAD51-...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337969/ https://www.ncbi.nlm.nih.gov/pubmed/32463460 http://dx.doi.org/10.1093/nar/gkaa406 |
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author | Shang, Yongliang Huang, Tao Liu, Hongbin Liu, Yanlei Liang, Heng Yu, Xiaoxia Li, Mengjing Zhai, Binyuan Yang, Xiao Wei, Yudong Wang, Guoqiang Chen, Zijiang Wang, Shunxin Zhang, Liangran |
author_facet | Shang, Yongliang Huang, Tao Liu, Hongbin Liu, Yanlei Liang, Heng Yu, Xiaoxia Li, Mengjing Zhai, Binyuan Yang, Xiao Wei, Yudong Wang, Guoqiang Chen, Zijiang Wang, Shunxin Zhang, Liangran |
author_sort | Shang, Yongliang |
collection | PubMed |
description | Repair of DNA double-strand breaks (DSBs) with homologous chromosomes is a hallmark of meiosis that is mediated by recombination ‘bridges’ between homolog axes. This process requires cooperation of DMC1 and RAD51 to promote homology search and strand exchange. The mechanism(s) regulating DMC1/RAD51-ssDNA nucleoprotein filament and the components of ‘bridges’ remain to be investigated. Here we show that MEIOK21 is a newly identified component of meiotic recombination bridges and is required for efficient formation of DMC1/RAD51 foci. MEIOK21 dynamically localizes on chromosomes from on-axis foci to ‘hanging foci’, then to ‘bridges’, and finally to ‘fused foci’ between homolog axes. Its chromosome localization depends on DSBs. Knockout of Meiok21 decreases the numbers of HSF2BP and DMC1/RAD51 foci, disrupting DSB repair, synapsis and crossover recombination and finally causing male infertility. Therefore, MEIOK21 is a novel recombination factor and probably mediates DMC1/RAD51 recruitment to ssDNA or their stability on chromosomes through physical interaction with HSF2BP. |
format | Online Article Text |
id | pubmed-7337969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73379692020-07-13 MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis Shang, Yongliang Huang, Tao Liu, Hongbin Liu, Yanlei Liang, Heng Yu, Xiaoxia Li, Mengjing Zhai, Binyuan Yang, Xiao Wei, Yudong Wang, Guoqiang Chen, Zijiang Wang, Shunxin Zhang, Liangran Nucleic Acids Res Genome Integrity, Repair and Replication Repair of DNA double-strand breaks (DSBs) with homologous chromosomes is a hallmark of meiosis that is mediated by recombination ‘bridges’ between homolog axes. This process requires cooperation of DMC1 and RAD51 to promote homology search and strand exchange. The mechanism(s) regulating DMC1/RAD51-ssDNA nucleoprotein filament and the components of ‘bridges’ remain to be investigated. Here we show that MEIOK21 is a newly identified component of meiotic recombination bridges and is required for efficient formation of DMC1/RAD51 foci. MEIOK21 dynamically localizes on chromosomes from on-axis foci to ‘hanging foci’, then to ‘bridges’, and finally to ‘fused foci’ between homolog axes. Its chromosome localization depends on DSBs. Knockout of Meiok21 decreases the numbers of HSF2BP and DMC1/RAD51 foci, disrupting DSB repair, synapsis and crossover recombination and finally causing male infertility. Therefore, MEIOK21 is a novel recombination factor and probably mediates DMC1/RAD51 recruitment to ssDNA or their stability on chromosomes through physical interaction with HSF2BP. Oxford University Press 2020-07-09 2020-05-28 /pmc/articles/PMC7337969/ /pubmed/32463460 http://dx.doi.org/10.1093/nar/gkaa406 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genome Integrity, Repair and Replication Shang, Yongliang Huang, Tao Liu, Hongbin Liu, Yanlei Liang, Heng Yu, Xiaoxia Li, Mengjing Zhai, Binyuan Yang, Xiao Wei, Yudong Wang, Guoqiang Chen, Zijiang Wang, Shunxin Zhang, Liangran MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis |
title | MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis |
title_full | MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis |
title_fullStr | MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis |
title_full_unstemmed | MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis |
title_short | MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis |
title_sort | meiok21: a new component of meiotic recombination bridges required for spermatogenesis |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337969/ https://www.ncbi.nlm.nih.gov/pubmed/32463460 http://dx.doi.org/10.1093/nar/gkaa406 |
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