Evidence map›Paper›PMID 23408915›Full record

ArticlePLoS genetics2013

Essential developmental, genomic stability, and tumour suppressor functions of the mouse orthologue of hSSB1/NABP2.

Wei Shi, Amanda L Bain, Bjoern Schwer, Fares Al-Ejeh, Corey Smith, Lee Wong, Hua Chai, Mariska S Miranda, Uda Ho, Makoto Kawaguchi and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2013. 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
2.4field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

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  12. Molecular basis of cleft palates in mice.World journal of biological chemistry · 2015
    Review
  13. Review
  14. Article
  15. Replication stress and cancer.Nature reviews. Cancer · 2015
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

18 authors at 9 institutions in 3 countries.

Wei ShiQueensland Institute of Medical Research, Herston, Australia.
Amanda L Bain
Bjoern Schwer
Fares Al-Ejeh
Corey Smith
Lee Wong
Hua Chai
Mariska S Miranda
Uda Ho
Makoto Kawaguchi
Yutaka Miura
John W Finnie
Meaghan Wall
Jörg Heierhorst
Carol Wicking
Kevin J Spring
Frederick W Alt
Kum Kum Khanna
QIMR Berghofer Medical Research Institute · AUNagoya City University · JPPediatrics and Genetics · USSt Vincent's Hospital · AUUniversity of Queensland · AUGriffith University · AUHarvard University · USMonash University · AUSouth Australia Pathology · AU

Funding

Molecular Mechanisms of Class Switch RecombinationR01AI077595 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI ALT, FREDERICK W. · 2009 to 2018
$4.3M
Pathobiology of Cancer at the Host and Population LevelT32CA009382 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI YUAN, ZHI-MIN · 1985 to 2012
$2.9M
Howard Hughes Medical InstituteNCI NIH HHS 5T32CA009382NCI NIH HHS T32 CA009382NIAID NIH HHS 5R01AI077595NIAID NIH HHS R01 AI077595
6 · The paper itself

Abstract

Single-stranded DNA binding proteins (SSBs) regulate multiple DNA transactions, including replication, transcription, and repair. We recently identified SSB1 as a novel protein critical for the initiation of ATM signaling and DNA double-strand break repair by homologous recombination. Here we report that germline Ssb1(-/-) embryos die at birth from respiratory failure due to severe rib cage malformation and impaired alveolar development, coupled with additional skeletal defects. Unexpectedly, Ssb1(-/-) fibroblasts did not exhibit defects in Atm signaling or γ-H2ax focus kinetics in response to ionizing radiation (IR), and B-cell specific deletion of Ssb1 did not affect class-switch recombination in vitro. However, conditional deletion of Ssb1 in adult mice led to increased cancer susceptibility with broad tumour spectrum, impaired male fertility with testicular degeneration, and increased radiosensitivity and IR-induced chromosome breaks in vivo. Collectively, these results demonstrate essential roles of Ssb1 in embryogenesis, spermatogenesis, and genome stability in vivo.

Indexed as

Carrier ProteinsDNA RepairNuclear ProteinsSuppressor of Cytokine Signaling ProteinsAnimalsB-LymphocytesChromosome BreakageDNA Breaks, Double-StrandedFibroblastsGene Expression Regulation, DevelopmentalGenomic InstabilityHistonesHomologous RecombinationHumansInfertility, MaleMaleATMIN protein, mouseCarrier Proteinsgamma-H2AX protein, mouseHistonesNuclear ProteinsSSB-1 protein, mouseSuppressor of Cytokine Signaling ProteinsTranscription Factors

Identifiers

PMID23408915
PMCPMC3567186
OpenAlexW2008848853

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.