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Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila
Topoisomerases solve topological problems during DNA metabolism, but whether they participate in RNA metabolism remains unclear. Top3β represents a family of topoisomerases carrying activities for both DNA and RNA. Here we show that in Drosophila, Top3β interacts biochemically and genetically with t...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251927/ https://www.ncbi.nlm.nih.gov/pubmed/30470739 http://dx.doi.org/10.1038/s41467-018-07101-4 |
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author | Lee, Seung Kyu Xue, Yutong Shen, Weiping Zhang, Yongqing Joo, Yuyoung Ahmad, Muzammil Chinen, Madoka Ding, Yi Ku, Wai Lim De, Supriyo Lehrmann, Elin Becker, Kevin G. Lei, Elissa P. Zhao, Keji Zou, Sige Sharov, Alexei Wang, Weidong |
author_facet | Lee, Seung Kyu Xue, Yutong Shen, Weiping Zhang, Yongqing Joo, Yuyoung Ahmad, Muzammil Chinen, Madoka Ding, Yi Ku, Wai Lim De, Supriyo Lehrmann, Elin Becker, Kevin G. Lei, Elissa P. Zhao, Keji Zou, Sige Sharov, Alexei Wang, Weidong |
author_sort | Lee, Seung Kyu |
collection | PubMed |
description | Topoisomerases solve topological problems during DNA metabolism, but whether they participate in RNA metabolism remains unclear. Top3β represents a family of topoisomerases carrying activities for both DNA and RNA. Here we show that in Drosophila, Top3β interacts biochemically and genetically with the RNAi-induced silencing complex (RISC) containing AGO2, p68 RNA helicase, and FMRP. Top3β and RISC mutants are similarly defective in heterochromatin formation and transcriptional silencing by position-effect variegation assay. Moreover, both Top3β and AGO2 mutants exhibit reduced levels of heterochromatin protein HP1 in heterochromatin. Furthermore, expression of several genes and transposable elements in heterochromatin is increased in the Top3β mutant. Notably, Top3β mutants defective in either RNA binding or catalytic activity are deficient in promoting HP1 recruitment and silencing of transposable elements. Our data suggest that Top3β may act as an RNA topoisomerase in siRNA-guided heterochromatin formation and transcriptional silencing. |
format | Online Article Text |
id | pubmed-6251927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62519272018-11-26 Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila Lee, Seung Kyu Xue, Yutong Shen, Weiping Zhang, Yongqing Joo, Yuyoung Ahmad, Muzammil Chinen, Madoka Ding, Yi Ku, Wai Lim De, Supriyo Lehrmann, Elin Becker, Kevin G. Lei, Elissa P. Zhao, Keji Zou, Sige Sharov, Alexei Wang, Weidong Nat Commun Article Topoisomerases solve topological problems during DNA metabolism, but whether they participate in RNA metabolism remains unclear. Top3β represents a family of topoisomerases carrying activities for both DNA and RNA. Here we show that in Drosophila, Top3β interacts biochemically and genetically with the RNAi-induced silencing complex (RISC) containing AGO2, p68 RNA helicase, and FMRP. Top3β and RISC mutants are similarly defective in heterochromatin formation and transcriptional silencing by position-effect variegation assay. Moreover, both Top3β and AGO2 mutants exhibit reduced levels of heterochromatin protein HP1 in heterochromatin. Furthermore, expression of several genes and transposable elements in heterochromatin is increased in the Top3β mutant. Notably, Top3β mutants defective in either RNA binding or catalytic activity are deficient in promoting HP1 recruitment and silencing of transposable elements. Our data suggest that Top3β may act as an RNA topoisomerase in siRNA-guided heterochromatin formation and transcriptional silencing. Nature Publishing Group UK 2018-11-23 /pmc/articles/PMC6251927/ /pubmed/30470739 http://dx.doi.org/10.1038/s41467-018-07101-4 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Lee, Seung Kyu Xue, Yutong Shen, Weiping Zhang, Yongqing Joo, Yuyoung Ahmad, Muzammil Chinen, Madoka Ding, Yi Ku, Wai Lim De, Supriyo Lehrmann, Elin Becker, Kevin G. Lei, Elissa P. Zhao, Keji Zou, Sige Sharov, Alexei Wang, Weidong Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila |
title | Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila |
title_full | Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila |
title_fullStr | Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila |
title_full_unstemmed | Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila |
title_short | Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila |
title_sort | topoisomerase 3β interacts with rnai machinery to promote heterochromatin formation and transcriptional silencing in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251927/ https://www.ncbi.nlm.nih.gov/pubmed/30470739 http://dx.doi.org/10.1038/s41467-018-07101-4 |
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