Compromised repair of radiation-induced DNA double-strand breaks in Fanconi anemia fibroblasts in G2.


Journal

DNA repair
ISSN: 1568-7856
Titre abrégé: DNA Repair (Amst)
Pays: Netherlands
ID NLM: 101139138

Informations de publication

Date de publication:
12 2020
Historique:
received: 15 06 2020
revised: 04 09 2020
accepted: 23 09 2020
pubmed: 18 10 2020
medline: 1 4 2021
entrez: 17 10 2020
Statut: ppublish

Résumé

Fanconi anemia (FA) is a rare chromosomal instability syndrome with various clinical features and high cancer incidence. Despite being a DNA repair disorder syndrome and a frequently observed clinical hypersensitivity of FA patients towards ionizing radiation, the experimental evidence regarding the efficiency of radiation-induced DNA double-strand break (DSB) repair in FA is very controversial. Here, we performed a thorough analysis of the repair of radiation-induced DSBs in G1 and G2 in FA fibroblasts of complementation groups A, C, D1 (BRCA2), D2, E, F, G and P (SLX4) in comparison to normal human lung and skin fibroblasts. γH2AX, 53BP1, or RPA foci quantification after X-irradiation was combined with cell cycle markers. Cytogenetic analyses were performed on first metaphases after irradiation in G1 and by premature chromosome condensation after exposure in G2. Furthermore, the role of canonical-NHEJ and alternative-NHEJ for the fidelity of the repair of radiation-induced DSBs was examined. In FA fibroblasts, DSB repair was normal in G1 but compromised and more error-prone in the slow repair component of G2 as suggested by higher yields of radiation-induced γH2AX and 53BP1 foci as well as chromatid exchanges. However, RPA foci quantification in G2 indicated proficiency for homology-directed repair of DSBs in FA except for FA D1 (BRCA2). In lung fibroblasts, DSB repair in G1 was conducted with normal kinetics but elevated chromosome exchanges compared to skin fibroblasts. The overall repair of radiation-induced DSBs and the formation of chromosome exchanges in normal and FA fibroblasts in G1 and G2 were governed by canonical-NHEJ with no contribution of alternative-NHEJ. Together, we show impaired repair of radiation-induced DSBs in various FA complementation groups in the slow repair component of G2 that might promote the formation of potentially oncogenic aberrations and clinical radiation hypersensitivity.

Identifiants

pubmed: 33069004
pii: S1568-7864(20)30251-2
doi: 10.1016/j.dnarep.2020.102992
pii:
doi:

Substances chimiques

BRCA2 Protein 0
BRCA2 protein, human 0
FANCA protein, human 0
FANCC protein, human 0
FANCD2 protein, human 0
FANCE protein, human 0
FANCF protein, human 0
FANCG protein, human 0
Fanconi Anemia Complementation Group A Protein 0
Fanconi Anemia Complementation Group C Protein 0
Fanconi Anemia Complementation Group D2 Protein 0
Fanconi Anemia Complementation Group E Protein 0
Fanconi Anemia Complementation Group F Protein 0
Fanconi Anemia Complementation Group G Protein 0
H2AX protein, human 0
Histones 0
Recombinases 0
TP53BP1 protein, human 0
Tumor Suppressor p53-Binding Protein 1 0
DNA 9007-49-2
SLX4 protein, human EC 3.1.-

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102992

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Sebastian Zahnreich (S)

Department of Radiation Oncology and Radiation Therapy, University Medical Centre of the Johannes Gutenberg, University Mainz, Germany. Electronic address: zahnreic@uni-mainz.de.

Britta Weber (B)

Department of Radiation Oncology and Radiation Therapy, University Medical Centre of the Johannes Gutenberg, University Mainz, Germany.

Gundula Rösch (G)

Department of Radiation Oncology and Radiation Therapy, University Medical Centre of the Johannes Gutenberg, University Mainz, Germany.

Detlev Schindler (D)

Institute of Human Genetics, Julius-Maximilians-University, Würzburg, Germany.

Heinz Schmidberger (H)

Department of Radiation Oncology and Radiation Therapy, University Medical Centre of the Johannes Gutenberg, University Mainz, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH