qDSB-Seq is a general method for genome-wide quantification of DNA double-strand breaks using sequencing.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
24 05 2019
Historique:
received: 01 02 2019
accepted: 30 04 2019
entrez: 26 5 2019
pubmed: 28 5 2019
medline: 7 6 2019
Statut: epublish

Résumé

DNA double-strand breaks (DSBs) are among the most lethal types of DNA damage and frequently cause genome instability. Sequencing-based methods for mapping DSBs have been developed but they allow measurement only of relative frequencies of DSBs between loci, which limits our understanding of the physiological relevance of detected DSBs. Here we propose quantitative DSB sequencing (qDSB-Seq), a method providing both DSB frequencies per cell and their precise genomic coordinates. We induce spike-in DSBs by a site-specific endonuclease and use them to quantify detected DSBs (labeled, e.g., using i-BLESS). Utilizing qDSB-Seq, we determine numbers of DSBs induced by a radiomimetic drug and replication stress, and reveal two orders of magnitude differences in DSB frequencies. We also measure absolute frequencies of Top1-dependent DSBs at natural replication fork barriers. qDSB-Seq is compatible with various DSB labeling methods in different organisms and allows accurate comparisons of absolute DSB frequencies across samples.

Identifiants

pubmed: 31127121
doi: 10.1038/s41467-019-10332-8
pii: 10.1038/s41467-019-10332-8
pmc: PMC6534554
doi:

Substances chimiques

DNA Topoisomerases, Type I EC 5.99.1.2
TOP1 protein, human EC 5.99.1.2

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2313

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM112131
Pays : United States
Organisme : U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS)
ID : R01 GM112131
Pays : International
Organisme : Fundacja na rzecz Nauki Polskiej (Foundation for Polish Science)
ID : TEAM/2016-2
Pays : International
Organisme : Ligue Contre le Cancer
ID : Equipe labelisée
Pays : International

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Auteurs

Yingjie Zhu (Y)

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA.

Anna Biernacka (A)

Laboratory of Bioinformatics and Systems Biology, Centre of New Technologies, University of Warsaw, Zwirki i Wigury 93, 02-089, Warsaw, Poland.

Benjamin Pardo (B)

Institut de Génétique Humaine, CNRS, Equipe Labellisée Ligue contre le Cancer, Université de Montpellier, 141 rue de la Cardonille, Montpellier, 34396, France.

Norbert Dojer (N)

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA.
Institute of Informatics, University of Warsaw, Stefana Banacha 2, 02-097, Warsaw, Poland.

Romain Forey (R)

Institut de Génétique Humaine, CNRS, Equipe Labellisée Ligue contre le Cancer, Université de Montpellier, 141 rue de la Cardonille, Montpellier, 34396, France.

Magdalena Skrzypczak (M)

Laboratory of Bioinformatics and Systems Biology, Centre of New Technologies, University of Warsaw, Zwirki i Wigury 93, 02-089, Warsaw, Poland.

Bernard Fongang (B)

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA.

Jules Nde (J)

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA.

Razie Yousefi (R)

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA.

Philippe Pasero (P)

Institut de Génétique Humaine, CNRS, Equipe Labellisée Ligue contre le Cancer, Université de Montpellier, 141 rue de la Cardonille, Montpellier, 34396, France.

Krzysztof Ginalski (K)

Laboratory of Bioinformatics and Systems Biology, Centre of New Technologies, University of Warsaw, Zwirki i Wigury 93, 02-089, Warsaw, Poland.

Maga Rowicka (M)

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA. Maga.Rowicka@utmb.edu.
Institute for Translational Sciences, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA. Maga.Rowicka@utmb.edu.
Sealy Center for Molecular Medicine, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, Texas, 77555, USA. Maga.Rowicka@utmb.edu.
Sealy Center for Structural Biology and Molecular Biophysics, University of Texas Medical Branch at Galveston, 301 University Boulevard, Galveston, TX, 77555, USA. Maga.Rowicka@utmb.edu.

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Classifications MeSH