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Multistep mechanism of G-quadruplex resolution during DNA replication
G-quadruplex (or G4) structures form in guanine-rich DNA sequences and threaten genome stability when not properly resolved. G4 unwinding occurs during S phase via an unknown mechanism. Using Xenopus egg extracts, we define a three-step G4 unwinding mechanism that acts during DNA replication. First,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462899/ https://www.ncbi.nlm.nih.gov/pubmed/34559566 http://dx.doi.org/10.1126/sciadv.abf8653 |
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author | Sato, Koichi Martin-Pintado, Nerea Post, Harm Altelaar, Maarten Knipscheer, Puck |
author_facet | Sato, Koichi Martin-Pintado, Nerea Post, Harm Altelaar, Maarten Knipscheer, Puck |
author_sort | Sato, Koichi |
collection | PubMed |
description | G-quadruplex (or G4) structures form in guanine-rich DNA sequences and threaten genome stability when not properly resolved. G4 unwinding occurs during S phase via an unknown mechanism. Using Xenopus egg extracts, we define a three-step G4 unwinding mechanism that acts during DNA replication. First, the replicative helicase composed of Cdc45, MCM2-7 and GINS (CMG) stalls at a leading strand G4 structure. Second, the DEAH-box helicase 36 (DHX36) mediates bypass of the CMG past the intact G4 structure, allowing approach of the leading strand to the G4. Third, G4 structure unwinding by the Fanconi anemia complementation group J helicase (FANCJ) enables DNA polymerase to synthesize past the G4 motif. A G4 on the lagging strand template does not stall CMG but still requires DNA replication for unwinding. DHX36 and FANCJ have partially redundant roles, conferring pathway robustness. This previously unknown genome maintenance pathway promotes faithful G4 replication, thereby avoiding genome instability. |
format | Online Article Text |
id | pubmed-8462899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84628992021-10-01 Multistep mechanism of G-quadruplex resolution during DNA replication Sato, Koichi Martin-Pintado, Nerea Post, Harm Altelaar, Maarten Knipscheer, Puck Sci Adv Biomedicine and Life Sciences G-quadruplex (or G4) structures form in guanine-rich DNA sequences and threaten genome stability when not properly resolved. G4 unwinding occurs during S phase via an unknown mechanism. Using Xenopus egg extracts, we define a three-step G4 unwinding mechanism that acts during DNA replication. First, the replicative helicase composed of Cdc45, MCM2-7 and GINS (CMG) stalls at a leading strand G4 structure. Second, the DEAH-box helicase 36 (DHX36) mediates bypass of the CMG past the intact G4 structure, allowing approach of the leading strand to the G4. Third, G4 structure unwinding by the Fanconi anemia complementation group J helicase (FANCJ) enables DNA polymerase to synthesize past the G4 motif. A G4 on the lagging strand template does not stall CMG but still requires DNA replication for unwinding. DHX36 and FANCJ have partially redundant roles, conferring pathway robustness. This previously unknown genome maintenance pathway promotes faithful G4 replication, thereby avoiding genome instability. American Association for the Advancement of Science 2021-09-24 /pmc/articles/PMC8462899/ /pubmed/34559566 http://dx.doi.org/10.1126/sciadv.abf8653 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). 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 use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Sato, Koichi Martin-Pintado, Nerea Post, Harm Altelaar, Maarten Knipscheer, Puck Multistep mechanism of G-quadruplex resolution during DNA replication |
title | Multistep mechanism of G-quadruplex resolution during DNA replication |
title_full | Multistep mechanism of G-quadruplex resolution during DNA replication |
title_fullStr | Multistep mechanism of G-quadruplex resolution during DNA replication |
title_full_unstemmed | Multistep mechanism of G-quadruplex resolution during DNA replication |
title_short | Multistep mechanism of G-quadruplex resolution during DNA replication |
title_sort | multistep mechanism of g-quadruplex resolution during dna replication |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462899/ https://www.ncbi.nlm.nih.gov/pubmed/34559566 http://dx.doi.org/10.1126/sciadv.abf8653 |
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