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Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing
The Hop2–Mnd1 complex functions with the DMC1 recombinase in meiotic recombination. Hop2–Mnd1 stabilizes the DMC1-single-stranded DNA (ssDNA) filament and promotes the capture of the double-stranded DNA partner by the recombinase filament to assemble the synaptic complex. Herein, we define the actio...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902922/ https://www.ncbi.nlm.nih.gov/pubmed/24150939 http://dx.doi.org/10.1093/nar/gkt924 |
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author | Zhao, Weixing Saro, Dorina Hammel, Michal Kwon, YoungHo Xu, Yuanyuan Rambo, Robert P. Williams, Gareth J. Chi, Peter Lu, Lucy Pezza, Roberto J. Camerini-Otero, R. Daniel Tainer, John A. Wang, Hong-Wei Sung, Patrick |
author_facet | Zhao, Weixing Saro, Dorina Hammel, Michal Kwon, YoungHo Xu, Yuanyuan Rambo, Robert P. Williams, Gareth J. Chi, Peter Lu, Lucy Pezza, Roberto J. Camerini-Otero, R. Daniel Tainer, John A. Wang, Hong-Wei Sung, Patrick |
author_sort | Zhao, Weixing |
collection | PubMed |
description | The Hop2–Mnd1 complex functions with the DMC1 recombinase in meiotic recombination. Hop2–Mnd1 stabilizes the DMC1-single-stranded DNA (ssDNA) filament and promotes the capture of the double-stranded DNA partner by the recombinase filament to assemble the synaptic complex. Herein, we define the action mechanism of Hop2–Mnd1 in DMC1-mediated recombination. Small angle X-ray scattering analysis and electron microscopy reveal that the heterodimeric Hop2–Mnd1 is a V-shaped molecule. We show that the protein complex harbors three distinct DNA binding sites, and determine their functional relevance. Specifically, the N-terminal double-stranded DNA binding functions of Hop2 and Mnd1 co-operate to mediate synaptic complex assembly, whereas ssDNA binding by the Hop2 C-terminus helps stabilize the DMC1-ssDNA filament. A model of the Hop2-Mnd1-DMC1-ssDNA ensemble is proposed to explain how it mediates homologous DNA pairing in meiotic recombination. |
format | Online Article Text |
id | pubmed-3902922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39029222014-01-27 Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing Zhao, Weixing Saro, Dorina Hammel, Michal Kwon, YoungHo Xu, Yuanyuan Rambo, Robert P. Williams, Gareth J. Chi, Peter Lu, Lucy Pezza, Roberto J. Camerini-Otero, R. Daniel Tainer, John A. Wang, Hong-Wei Sung, Patrick Nucleic Acids Res Genome Integrity, Repair and Replication The Hop2–Mnd1 complex functions with the DMC1 recombinase in meiotic recombination. Hop2–Mnd1 stabilizes the DMC1-single-stranded DNA (ssDNA) filament and promotes the capture of the double-stranded DNA partner by the recombinase filament to assemble the synaptic complex. Herein, we define the action mechanism of Hop2–Mnd1 in DMC1-mediated recombination. Small angle X-ray scattering analysis and electron microscopy reveal that the heterodimeric Hop2–Mnd1 is a V-shaped molecule. We show that the protein complex harbors three distinct DNA binding sites, and determine their functional relevance. Specifically, the N-terminal double-stranded DNA binding functions of Hop2 and Mnd1 co-operate to mediate synaptic complex assembly, whereas ssDNA binding by the Hop2 C-terminus helps stabilize the DMC1-ssDNA filament. A model of the Hop2-Mnd1-DMC1-ssDNA ensemble is proposed to explain how it mediates homologous DNA pairing in meiotic recombination. Oxford University Press 2014-01 2013-10-21 /pmc/articles/PMC3902922/ /pubmed/24150939 http://dx.doi.org/10.1093/nar/gkt924 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Genome Integrity, Repair and Replication Zhao, Weixing Saro, Dorina Hammel, Michal Kwon, YoungHo Xu, Yuanyuan Rambo, Robert P. Williams, Gareth J. Chi, Peter Lu, Lucy Pezza, Roberto J. Camerini-Otero, R. Daniel Tainer, John A. Wang, Hong-Wei Sung, Patrick Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing |
title | Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing |
title_full | Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing |
title_fullStr | Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing |
title_full_unstemmed | Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing |
title_short | Mechanistic insights into the role of Hop2–Mnd1 in meiotic homologous DNA pairing |
title_sort | mechanistic insights into the role of hop2–mnd1 in meiotic homologous dna pairing |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902922/ https://www.ncbi.nlm.nih.gov/pubmed/24150939 http://dx.doi.org/10.1093/nar/gkt924 |
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