<scp>WRN</scp> helicase and mismatch repair complexes independently and synergistically disrupt cruciform <scp>DNA</scp> structures-Reference-Cited by-同舟云学术

WRN helicase and mismatch repair complexes independently and synergistically disrupt cruciform DNA structures

Published:2022-12-21 Issue:3 Volume:42 Page:
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:The EMBO Journal

Author:

Mengoli Valentina¹,Ceppi Ilaria¹^ORCID,Sanchez Aurore¹,Cannavo Elda¹,Halder Swagata¹,Scaglione Sarah²^ORCID,Gaillard Pierre‐Henri²^ORCID,McHugh Peter J³^ORCID,Riesen Nathalie⁴,Pettazzoni Piergiorgio⁴^ORCID,Cejka Petr¹⁵^ORCID

Affiliation:

1. Faculty of Biomedical Sciences, Institute for Research in Biomedicine Università della Svizzera italiana (USI) Bellinzona Switzerland

2. Centre de Recherche en Cancérologie de Marseille, CRCM, Inserm, CNRS, Aix‐Marseille Université, Institut Paoli‐Calmettes Marseille France

3. Department of Oncology, MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital University of Oxford Oxford UK

4. Roche Pharma Research & Early Development pRED Roche Innovation Center Basel Switzerland

5. Department of Biology, Institute of Biochemistry Eidgenössische Technische Hochschule (ETH) Zürich Switzerland

Funder

Institut National Du Cancer

Krebsliga Schweiz

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

EMBO

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embj.2022111998

Reference58 articles.

1. Regulation of WRN Helicase Activity in Human Base Excision Repair

2. RAD51 and mitotic function of mus81 are essential for recovery from low-dose of camptothecin in the absence of the WRN exonuclease

3. ATR and ATM differently regulate WRN to prevent DSBs at stalled replication forks and promote replication fork recovery

4. Phosphorylated CtIP Functions as a Co-factor of the MRE11-RAD50-NBS1 Endonuclease in DNA End Resection

5. Methods to Study DNA End Resection I: Recombinant Protein Purification

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