Evidence map›Paper›PMID 25833379›Full record

ReviewOpen biology2015

Ubiquitylation, neddylation and the DNA damage response.

Jessica S Brown, Stephen P Jackson

Open access · goldAbstract readReview
In one paragraph

Review in Open biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

90 citing papers in PubMed, 142 citations in OpenAlex.

  1. Review
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  12. DNA damage-induced proteasome phosphorylation controls substrate recognition and facilitates DNA repair.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Review
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  16. Article
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  18. Review
  19. Article
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30 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 2 countries.

Jessica S BrownThe Wellcome Trust and Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.
Stephen P JacksonThe Wellcome Trust and Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK s.jackson@gurdon.cam.ac.uk.
University of Cambridge · GBWellcome/Cancer Research UK Gurdon Institute · GB

Funding

Cancer Research UK 11224Cancer Research UK 18796Cancer Research UK C6/A11224Wellcome Trust 094794/Z/10/ZWellcome Trust WT092096
6 · The paper itself

Abstract

Failure of accurate DNA damage sensing and repair mechanisms manifests as a variety of human diseases, including neurodegenerative disorders, immunodeficiency, infertility and cancer. The accuracy and efficiency of DNA damage detection and repair, collectively termed the DNA damage response (DDR), requires the recruitment and subsequent post-translational modification (PTM) of a complex network of proteins. Ubiquitin and the ubiquitin-like protein (UBL) SUMO have established roles in regulating the cellular response to DNA double-strand breaks (DSBs). A role for other UBLs, such as NEDD8, is also now emerging. This article provides an overview of the DDR, discusses our current understanding of the process and function of PTM by ubiquitin and NEDD8, and reviews the literature surrounding the role of ubiquitylation and neddylation in DNA repair processes, focusing particularly on DNA DSB repair.

Indexed as

DNA DamageDNA RepairProtein Processing, Post-TranslationalUbiquitinationDNADNA-Binding ProteinsHumansModels, GeneticNEDD8 ProteinUbiquitin-Protein LigasesUbiquitinsDNADNA-Binding ProteinsNEDD8 ProteinNEDD8 protein, humanUbiquitin-Protein LigasesUbiquitinsDNA damage responsedouble-strand break repairMLN4924NEDD8ubiquitin

Identifiers

PMID25833379
PMCPMC4422126
OpenAlexW2149296898

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.