Evidence map›Paper›PMID 31501324›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Evolution-based screening enables genome-wide prioritization and discovery of DNA repair genes.

Gregory J Brunette, Mohd A Jamalruddin, Robert A Baldock, Nathan L Clark, Kara A Bernstein

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

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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.

Gregory J BrunetteDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213.ORCID 0000-0002-3829-9031
Mohd A JamalruddinDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213.
Robert A BaldockSchool of Sport, Health and Social Sciences, Solent University, Southampton SO14 0YN, United Kingdom.
Nathan L ClarkDepartment of Computational and Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213.ORCID 0000-0003-0006-8374
Kara A BernsteinDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213; karab@pitt.edu.

Funding

Title: Functional Annotation of Genomes via Phenotypic Convergence within Large Multi-species AlignmentsR01HG009299 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Maria D Chikina, Nathaniel L Clark · 2017 to 2026
$4.1M
Replication fork dynamics and repair by Rad51 paralogues after DNA alkylationR01ES024872 · NIEHS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BERNSTEIN, KARA A · 2015 to 2019
$2.4M
NHGRI NIH HHS R01 HG009299NIEHS NIH HHS R01 ES024872
6 · The paper itself

Abstract

DNA repair is critical for genome stability and is maintained through conserved pathways. Traditional genome-wide mammalian screens are both expensive and laborious. However, computational approaches circumvent these limitations and are a powerful tool to identify new DNA repair factors. By analyzing the evolutionary relationships between genes in the major DNA repair pathways, we uncovered functional relationships between individual genes and identified partners. Here we ranked 17,487 mammalian genes for coevolution with 6 distinct DNA repair pathways. Direct comparison to genetic screens for homologous recombination or Fanconi anemia factors indicates that our evolution-based screen is comparable, if not superior, to traditional screening approaches. Demonstrating the utility of our strategy, we identify a role for the DNA damage-induced apoptosis suppressor (

Indexed as

AnimalsApoptosis Regulatory ProteinsCell Cycle ProteinsDNA Breaks, Double-StrandedDNA RepairEvolution, MolecularGenome-Wide Association StudyGenomic InstabilityHomologous RecombinationHumansRad51 RecombinaseApoptosis Regulatory ProteinsCell Cycle ProteinsDDIAS protein, humanRad51 RecombinaseDDIASDNA repairevolutiongenome integrityhomologous recombination

Identifiers

PMID31501324
PMCPMC6765268

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.