Evidence map›Paper›PMID 29294118›Full record

ArticleNucleic acids research2018

Direct observation of end resection by RecBCD during double-stranded DNA break repair in vivo.

Jakub Wiktor, Marit van der Does, Lisa Büller, David J Sherratt, Cees Dekker

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  3. SMC protein RecN drives RecA filament translocation for in vivo homology search.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  16. Assessing Protein Dynamics on Low-Complexity Single-Stranded DNA Curtains.Langmuir : the ACS journal of surfaces and colloids · 2018
    Article
  17. Phage Mu Gam protein promotes NHEJ in concert withProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Jakub WiktorDepartment of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Marit van der DoesDepartment of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Lisa BüllerDepartment of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, 2629 HZ Delft, The Netherlands.
David J SherrattDepartment of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.
Cees DekkerDepartment of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Delft University of Technology · NLUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I004785/1European Research Council 247072Wellcome Trust 200782/Z/16/Z
6 · The paper itself

Abstract

The formation of 3' single-stranded DNA overhangs is a first and essential step during homology-directed repair of double-stranded breaks (DSB) of DNA, a task that in Escherichia coli is performed by RecBCD. While this protein complex has been well characterized through in vitro single-molecule studies, it has remained elusive how end resection proceeds in the crowded and complex environment in live cells. Here, we develop a two-color fluorescent reporter to directly observe the resection of individual inducible DSB sites within live E. coli cells. Real-time imaging shows that RecBCD during end resection degrades DNA with remarkably high speed (∼1.6 kb/s) and high processivity (>∼100 kb). The results show a pronounced asymmetry in the processing of the two DNA ends of a DSB, where much longer stretches of DNA are degraded in the direction of terminus. The microscopy observations are confirmed using quantitative polymerase chain reaction measurements of the DNA degradation. Deletion of the recD gene drastically decreased the length of resection, allowing for recombination with short ectopic plasmid homologies and significantly increasing the efficiency of horizontal gene transfer between strains. We thus visualized and quantified DNA end resection by the RecBCD complex in live cells, recorded DNA-degradation linked to end resection and uncovered a general relationship between the length of end resection and the choice of the homologous recombination template.

Indexed as

DNA Breaks, Double-StrandedDNA RepairDeoxyribonucleases, Type II Site-SpecificDNA, BacterialEscherichia coliEscherichia coli ProteinsExodeoxyribonuclease VGene DeletionGene Transfer, HorizontalLuminescent ProteinsMicroscopy, FluorescenceReal-Time Polymerase Chain ReactionSaccharomyces cerevisiae ProteinsDeoxyribonucleases, Type II Site-SpecificDNA, BacterialEscherichia coli ProteinsExodeoxyribonuclease Vexodeoxyribonuclease V, E coliLuminescent ProteinsSaccharomyces cerevisiae ProteinsSCEI protein, S cerevisiae

Identifiers

PMID29294118
PMCPMC5829741
OpenAlexW2777650842

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.