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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9684126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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