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Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination
The long non-coding telomeric RNA transcript TERRA, in the form of an RNA–DNA duplex, regulates telomere recombination. In a screen for nucleases that affects telomere recombination, mutations in DNA2, EXO1, MRE11 and SAE2 cause severe delay in type II survivor formation, indicating that type II tel...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201435/ https://www.ncbi.nlm.nih.gov/pubmed/36999631 http://dx.doi.org/10.1093/nar/gkad236 |
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author | Liu, Chia-Chun Chan, Hsin-Ru Su, Guan-Chin Hsieh, Yan-Zhu Lei, Kai-Hang Kato, Tomoka Yu, Tai-Yuan Kao, Yu-wen Cheng, Tzu-Hao Chi, Peter Lin, Jing-Jer |
author_facet | Liu, Chia-Chun Chan, Hsin-Ru Su, Guan-Chin Hsieh, Yan-Zhu Lei, Kai-Hang Kato, Tomoka Yu, Tai-Yuan Kao, Yu-wen Cheng, Tzu-Hao Chi, Peter Lin, Jing-Jer |
author_sort | Liu, Chia-Chun |
collection | PubMed |
description | The long non-coding telomeric RNA transcript TERRA, in the form of an RNA–DNA duplex, regulates telomere recombination. In a screen for nucleases that affects telomere recombination, mutations in DNA2, EXO1, MRE11 and SAE2 cause severe delay in type II survivor formation, indicating that type II telomere recombination is mediated through a mechanism similar to repairing double-strand breaks. On the other hand, mutation in RAD27 results in early formation of type II recombination, suggesting that RAD27 acts as a negative regulator in telomere recombination. RAD27 encodes a flap endonuclease that plays a role in DNA metabolism, including replication, repair and recombination. We demonstrate that Rad27 suppresses the accumulation of the TERRA-associated R-loop and selectively cleaves TERRA of R-loop and double-flapped structures in vitro. Moreover, we show that Rad27 negatively regulates single-stranded C-rich telomeric DNA circles (C-circles) in telomerase-deficient cells, revealing a close correlation between R-loop and C-circles during telomere recombination. These results demonstrate that Rad27 participates in telomere recombination by cleaving TERRA in the context of an R-loop or flapped RNA–DNA duplex, providing mechanistic insight into how Rad27 maintains chromosome stability by restricting the accumulation of the R-loop structure within the genome. |
format | Online Article Text |
id | pubmed-10201435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102014352023-05-23 Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination Liu, Chia-Chun Chan, Hsin-Ru Su, Guan-Chin Hsieh, Yan-Zhu Lei, Kai-Hang Kato, Tomoka Yu, Tai-Yuan Kao, Yu-wen Cheng, Tzu-Hao Chi, Peter Lin, Jing-Jer Nucleic Acids Res Molecular Biology The long non-coding telomeric RNA transcript TERRA, in the form of an RNA–DNA duplex, regulates telomere recombination. In a screen for nucleases that affects telomere recombination, mutations in DNA2, EXO1, MRE11 and SAE2 cause severe delay in type II survivor formation, indicating that type II telomere recombination is mediated through a mechanism similar to repairing double-strand breaks. On the other hand, mutation in RAD27 results in early formation of type II recombination, suggesting that RAD27 acts as a negative regulator in telomere recombination. RAD27 encodes a flap endonuclease that plays a role in DNA metabolism, including replication, repair and recombination. We demonstrate that Rad27 suppresses the accumulation of the TERRA-associated R-loop and selectively cleaves TERRA of R-loop and double-flapped structures in vitro. Moreover, we show that Rad27 negatively regulates single-stranded C-rich telomeric DNA circles (C-circles) in telomerase-deficient cells, revealing a close correlation between R-loop and C-circles during telomere recombination. These results demonstrate that Rad27 participates in telomere recombination by cleaving TERRA in the context of an R-loop or flapped RNA–DNA duplex, providing mechanistic insight into how Rad27 maintains chromosome stability by restricting the accumulation of the R-loop structure within the genome. Oxford University Press 2023-03-31 /pmc/articles/PMC10201435/ /pubmed/36999631 http://dx.doi.org/10.1093/nar/gkad236 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), 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 | Molecular Biology Liu, Chia-Chun Chan, Hsin-Ru Su, Guan-Chin Hsieh, Yan-Zhu Lei, Kai-Hang Kato, Tomoka Yu, Tai-Yuan Kao, Yu-wen Cheng, Tzu-Hao Chi, Peter Lin, Jing-Jer Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination |
title | Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination |
title_full | Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination |
title_fullStr | Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination |
title_full_unstemmed | Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination |
title_short | Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination |
title_sort | flap endonuclease rad27 cleaves the rna of r-loop structures to suppress telomere recombination |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201435/ https://www.ncbi.nlm.nih.gov/pubmed/36999631 http://dx.doi.org/10.1093/nar/gkad236 |
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