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Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures

Smc5/6 is an evolutionarily conserved SMC complex with roles in DNA replication and repair, as well as in viral DNA restriction. Understanding its multiple functions has been hampered by a lack of mechanistic studies on how the Smc5/6 complex associates with different types of DNA. Here we address t...

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Autores principales: Chang, Jeremy T-H., Li, Shibai, Beckwitt, Emily C., Than, Thane, Haluska, Cory, Chandanani, Joshua, O’Donnell, Michael E., Zhao, Xiaolan, Liu, Shixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684126/
https://www.ncbi.nlm.nih.gov/pubmed/36418314
http://dx.doi.org/10.1038/s41467-022-34928-9
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author Chang, Jeremy T-H.
Li, Shibai
Beckwitt, Emily C.
Than, Thane
Haluska, Cory
Chandanani, Joshua
O’Donnell, Michael E.
Zhao, Xiaolan
Liu, Shixin
author_facet Chang, Jeremy T-H.
Li, Shibai
Beckwitt, Emily C.
Than, Thane
Haluska, Cory
Chandanani, Joshua
O’Donnell, Michael E.
Zhao, Xiaolan
Liu, Shixin
author_sort Chang, Jeremy T-H.
collection PubMed
description Smc5/6 is an evolutionarily conserved SMC complex with roles in DNA replication and repair, as well as in viral DNA restriction. Understanding its multiple functions has been hampered by a lack of mechanistic studies on how the Smc5/6 complex associates with different types of DNA. Here we address this question by simultaneously visualizing the behavior of Smc5/6 on three types of DNA, namely double-stranded (ds) DNA, single-stranded (ss) DNA, and junction DNA formed by juxtaposed ss- and dsDNA, using correlative single-molecule fluorescence and force microscopy. We find that Smc5/6 displays distinct behaviors toward different types of DNA, dynamically associating with dsDNA while stably binding to junction DNA. Mechanistically, both the Nse1-3-4 subcomplex and ATP binding enhance the complex’s dsDNA association. In contrast, Smc5/6’s assembly onto ssDNA emanating from junction DNA, which occurs even in the presence high-affinity ssDNA binders, is aided by Nse1-3-4, but not by ATP. Moreover, we show that Smc5/6 protects junction DNA stability by preventing ssDNA annealing. The multifaceted DNA association behaviors of Smc5/6 provide a framework for understanding its diverse functions in genome maintenance and viral DNA restriction.
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spelling pubmed-96841262022-11-25 Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures Chang, Jeremy T-H. Li, Shibai Beckwitt, Emily C. Than, Thane Haluska, Cory Chandanani, Joshua O’Donnell, Michael E. Zhao, Xiaolan Liu, Shixin Nat Commun Article Smc5/6 is an evolutionarily conserved SMC complex with roles in DNA replication and repair, as well as in viral DNA restriction. Understanding its multiple functions has been hampered by a lack of mechanistic studies on how the Smc5/6 complex associates with different types of DNA. Here we address this question by simultaneously visualizing the behavior of Smc5/6 on three types of DNA, namely double-stranded (ds) DNA, single-stranded (ss) DNA, and junction DNA formed by juxtaposed ss- and dsDNA, using correlative single-molecule fluorescence and force microscopy. We find that Smc5/6 displays distinct behaviors toward different types of DNA, dynamically associating with dsDNA while stably binding to junction DNA. Mechanistically, both the Nse1-3-4 subcomplex and ATP binding enhance the complex’s dsDNA association. In contrast, Smc5/6’s assembly onto ssDNA emanating from junction DNA, which occurs even in the presence high-affinity ssDNA binders, is aided by Nse1-3-4, but not by ATP. Moreover, we show that Smc5/6 protects junction DNA stability by preventing ssDNA annealing. The multifaceted DNA association behaviors of Smc5/6 provide a framework for understanding its diverse functions in genome maintenance and viral DNA restriction. Nature Publishing Group UK 2022-11-23 /pmc/articles/PMC9684126/ /pubmed/36418314 http://dx.doi.org/10.1038/s41467-022-34928-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chang, Jeremy T-H.
Li, Shibai
Beckwitt, Emily C.
Than, Thane
Haluska, Cory
Chandanani, Joshua
O’Donnell, Michael E.
Zhao, Xiaolan
Liu, Shixin
Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures
title Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures
title_full Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures
title_fullStr Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures
title_full_unstemmed Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures
title_short Smc5/6’s multifaceted DNA binding capacities stabilize branched DNA structures
title_sort smc5/6’s multifaceted dna binding capacities stabilize branched dna structures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684126/
https://www.ncbi.nlm.nih.gov/pubmed/36418314
http://dx.doi.org/10.1038/s41467-022-34928-9
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