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Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II
Etoposide is a broadly employed chemotherapeutic and eukaryotic topoisomerase II poison that stabilizes cleaved DNA intermediates to promote DNA breakage and cytotoxicity. How etoposide perturbs topoisomerase dynamics is not known. Here we investigated the action of etoposide on yeast topoisomerase...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154222/ https://www.ncbi.nlm.nih.gov/pubmed/36717711 http://dx.doi.org/10.1038/s41589-022-01235-9 |
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author | Le, Tung T. Wu, Meiling Lee, Joyce H. Bhatt, Neti Inman, James T. Berger, James M. Wang, Michelle D. |
author_facet | Le, Tung T. Wu, Meiling Lee, Joyce H. Bhatt, Neti Inman, James T. Berger, James M. Wang, Michelle D. |
author_sort | Le, Tung T. |
collection | PubMed |
description | Etoposide is a broadly employed chemotherapeutic and eukaryotic topoisomerase II poison that stabilizes cleaved DNA intermediates to promote DNA breakage and cytotoxicity. How etoposide perturbs topoisomerase dynamics is not known. Here we investigated the action of etoposide on yeast topoisomerase II, human topoisomerase IIα and human topoisomerase IIβ using several sensitive single-molecule detection methods. Unexpectedly, we found that etoposide induces topoisomerase to trap DNA loops, compacting DNA and restructuring DNA topology. Loop trapping occurs after ATP hydrolysis but before strand ejection from the enzyme. Although etoposide decreases the innate stability of topoisomerase dimers, it increases the ability of the enzyme to act as a stable roadblock. Interestingly, the three topoisomerases show similar etoposide-mediated resistance to dimer separation and sliding along DNA but different abilities to compact DNA and chirally relax DNA supercoils. These data provide unique mechanistic insights into the functional consequences of etoposide on topoisomerase II dynamics. [Image: see text] |
format | Online Article Text |
id | pubmed-10154222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-101542222023-05-04 Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II Le, Tung T. Wu, Meiling Lee, Joyce H. Bhatt, Neti Inman, James T. Berger, James M. Wang, Michelle D. Nat Chem Biol Article Etoposide is a broadly employed chemotherapeutic and eukaryotic topoisomerase II poison that stabilizes cleaved DNA intermediates to promote DNA breakage and cytotoxicity. How etoposide perturbs topoisomerase dynamics is not known. Here we investigated the action of etoposide on yeast topoisomerase II, human topoisomerase IIα and human topoisomerase IIβ using several sensitive single-molecule detection methods. Unexpectedly, we found that etoposide induces topoisomerase to trap DNA loops, compacting DNA and restructuring DNA topology. Loop trapping occurs after ATP hydrolysis but before strand ejection from the enzyme. Although etoposide decreases the innate stability of topoisomerase dimers, it increases the ability of the enzyme to act as a stable roadblock. Interestingly, the three topoisomerases show similar etoposide-mediated resistance to dimer separation and sliding along DNA but different abilities to compact DNA and chirally relax DNA supercoils. These data provide unique mechanistic insights into the functional consequences of etoposide on topoisomerase II dynamics. [Image: see text] Nature Publishing Group US 2023-01-30 2023 /pmc/articles/PMC10154222/ /pubmed/36717711 http://dx.doi.org/10.1038/s41589-022-01235-9 Text en © The Author(s) 2023 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 Le, Tung T. Wu, Meiling Lee, Joyce H. Bhatt, Neti Inman, James T. Berger, James M. Wang, Michelle D. Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II |
title | Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II |
title_full | Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II |
title_fullStr | Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II |
title_full_unstemmed | Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II |
title_short | Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II |
title_sort | etoposide promotes dna loop trapping and barrier formation by topoisomerase ii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154222/ https://www.ncbi.nlm.nih.gov/pubmed/36717711 http://dx.doi.org/10.1038/s41589-022-01235-9 |
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