Cargando…

Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA

G-quadruplexes (G4s) are non-canonical DNA structures with critical roles in DNA metabolisms. To resolve those structures that can cause replication fork stalling and genomic instability, single-stranded DNA-binding proteins and helicases are required. Here, we characterized the interplay between RP...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yi-Ran, Guo, Ting-Ting, Zheng, Ya-Ting, Lai, Chang-Wei, Sun, Bo, Xi, Xu-Guang, Hou, Xi-Miao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169993/
https://www.ncbi.nlm.nih.gov/pubmed/34113828
http://dx.doi.org/10.1016/j.isci.2021.102493
_version_ 1783702140594683904
author Wang, Yi-Ran
Guo, Ting-Ting
Zheng, Ya-Ting
Lai, Chang-Wei
Sun, Bo
Xi, Xu-Guang
Hou, Xi-Miao
author_facet Wang, Yi-Ran
Guo, Ting-Ting
Zheng, Ya-Ting
Lai, Chang-Wei
Sun, Bo
Xi, Xu-Guang
Hou, Xi-Miao
author_sort Wang, Yi-Ran
collection PubMed
description G-quadruplexes (G4s) are non-canonical DNA structures with critical roles in DNA metabolisms. To resolve those structures that can cause replication fork stalling and genomic instability, single-stranded DNA-binding proteins and helicases are required. Here, we characterized the interplay between RPA and helicases on G4s using single-molecule FRET. We first discovered that human RPA efficiently prevents G4 formation by preempting ssDNA before its folding. RPA also differentially interacts with the folded G4s. However, helicases such as human BLM and yeast Pif1 have different G4 preferences from RPA mainly based on loop lengths. More importantly, both RPA and these helicases are required for the stable G4 unfolding, as RPA promotes helicase-mediated repetitive unfolding into durative linear state. Furthermore, BLM can traverse G4 obstacles temporarily disrupted by RPA and continue to unwind downstream duplex. We finally proposed the mechanisms underlying above functions of RPA in preventing, resolving, and assisting helicases to eliminate G4s.
format Online
Article
Text
id pubmed-8169993
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-81699932021-06-09 Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA Wang, Yi-Ran Guo, Ting-Ting Zheng, Ya-Ting Lai, Chang-Wei Sun, Bo Xi, Xu-Guang Hou, Xi-Miao iScience Article G-quadruplexes (G4s) are non-canonical DNA structures with critical roles in DNA metabolisms. To resolve those structures that can cause replication fork stalling and genomic instability, single-stranded DNA-binding proteins and helicases are required. Here, we characterized the interplay between RPA and helicases on G4s using single-molecule FRET. We first discovered that human RPA efficiently prevents G4 formation by preempting ssDNA before its folding. RPA also differentially interacts with the folded G4s. However, helicases such as human BLM and yeast Pif1 have different G4 preferences from RPA mainly based on loop lengths. More importantly, both RPA and these helicases are required for the stable G4 unfolding, as RPA promotes helicase-mediated repetitive unfolding into durative linear state. Furthermore, BLM can traverse G4 obstacles temporarily disrupted by RPA and continue to unwind downstream duplex. We finally proposed the mechanisms underlying above functions of RPA in preventing, resolving, and assisting helicases to eliminate G4s. Elsevier 2021-05-01 /pmc/articles/PMC8169993/ /pubmed/34113828 http://dx.doi.org/10.1016/j.isci.2021.102493 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Wang, Yi-Ran
Guo, Ting-Ting
Zheng, Ya-Ting
Lai, Chang-Wei
Sun, Bo
Xi, Xu-Guang
Hou, Xi-Miao
Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA
title Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA
title_full Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA
title_fullStr Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA
title_full_unstemmed Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA
title_short Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA
title_sort replication protein a plays multifaceted roles complementary to specialized helicases in processing g-quadruplex dna
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169993/
https://www.ncbi.nlm.nih.gov/pubmed/34113828
http://dx.doi.org/10.1016/j.isci.2021.102493
work_keys_str_mv AT wangyiran replicationproteinaplaysmultifacetedrolescomplementarytospecializedhelicasesinprocessinggquadruplexdna
AT guotingting replicationproteinaplaysmultifacetedrolescomplementarytospecializedhelicasesinprocessinggquadruplexdna
AT zhengyating replicationproteinaplaysmultifacetedrolescomplementarytospecializedhelicasesinprocessinggquadruplexdna
AT laichangwei replicationproteinaplaysmultifacetedrolescomplementarytospecializedhelicasesinprocessinggquadruplexdna
AT sunbo replicationproteinaplaysmultifacetedrolescomplementarytospecializedhelicasesinprocessinggquadruplexdna
AT xixuguang replicationproteinaplaysmultifacetedrolescomplementarytospecializedhelicasesinprocessinggquadruplexdna
AT houximiao replicationproteinaplaysmultifacetedrolescomplementarytospecializedhelicasesinprocessinggquadruplexdna