Evidence map›Paper›PMID 35027540›Full record

ArticleNature communications2022

Linking DNA repair and cell cycle progression through serine ADP-ribosylation of histones.

Julien Brustel, Tetsuya Muramoto, Kazuki Fumimoto, Jessica Ellins, Catherine J Pears, Nicholas D Lakin

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.2field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Oxphos targeting ofFrontiers in oncology · 2025
    Article
  7. Article
  8. Review
  9. Review
  10. Mitotic chromatin marking governs asymmetric segregation of DNA damage.bioRxiv : the preprint server for biology · 2024
    Article
  11. Review
  12. Article
  13. Histone ADP-ribosylation promotes resistance to PARP inhibitors by facilitating PARP1 release from DNA lesions.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Solid-Phase Synthesis and Biological Evaluation of Peptides ADP-Ribosylated at Histidine.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2024
    Article
  15. Article
  16. Article
  17. EdeepSADPr: an extensive deep-learning architecture for prediction of theFrontiers in cell and developmental biology · 2023
    Article
  18. Review
  19. Review
  20. 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

6 authors at 2 institutions in 2 countries.

Julien BrustelDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford, UK.
Tetsuya MuramotoDepartment of Biology, Faculty of Science, Toho University, Funabashi, Chiba, Japan.ORCID http://orcid.org/0000-0001-9624-8577
Kazuki FumimotoDepartment of Biology, Faculty of Science, Toho University, Funabashi, Chiba, Japan.
Jessica EllinsDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford, UK.
Catherine J PearsDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford, UK.ORCID http://orcid.org/0000-0003-1290-8326
Nicholas D LakinDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford, UK. nicholas.lakin@bioch.ox.ac.uk.ORCID http://orcid.org/0000-0003-4999-5814
University of Oxford · GBToho University · JP

Funding

Medical Research Council MR/P028284/1Medical Research Council MR/V00896X/1Medical Research Council MR/W017350/1
6 · The paper itself

Abstract

Although serine ADP-ribosylation (Ser-ADPr) by Poly(ADP-ribose)-polymerases is a cornerstone of the DNA damage response, how this regulates DNA repair and genome stability is unknown. Here, we exploit the ability to manipulate histone genes in Dictyostelium to identify that ADPr of the histone variant H3b at S10 and S28 maintains genome stability by integrating double strand break (DSB) repair with mitotic entry. Given the critical requirement for mitotic H3S10/28 phosphorylation, we develop separation of function mutations that maintain S10 phosphorylation whilst disrupting ADPr. Mechanistically, this reveals a requirement for H3bS10/28 ADPr in non-homologous end-joining by recruiting Ku to DSBs. Moreover, this also identifies H3bS10/S28 ADPr is critical to prevent premature mitotic entry with unresolved DNA damage, thus maintaining genome stability. Together, these data demonstrate how serine ADPr of histones coordinates DNA repair with cell cycle progression to maintain genome stability.

Indexed as

Protein Processing, Post-TranslationalADP-RibosylationCell CycleDictyosteliumDNA Breaks, Double-StrandedDNA DamageDNA End-Joining RepairDNA, ProtozoanGenomic InstabilityHistonesKu AutoantigenPhosphorylationPoly(ADP-ribose) PolymerasesSerineDNA, ProtozoanHistonesKu AutoantigenPoly(ADP-ribose) PolymerasesSerine

Identifiers

PMID35027540
PMCPMC8758696
OpenAlexW4206680490

What OpenQuestion holds

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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.