Evidence map›Paper›PMID 35298257›Full record

ArticleScience (New York, N.Y.)2022

The histone H3.1 variant regulates TONSOKU-mediated DNA repair during replication.

Hossein Davarinejad, Yi-Chun Huang, Benoit Mermaz, Chantal LeBlanc, Axel Poulet, Geoffrey Thomson, Valentin Joly, Marcelo Muñoz, Alexis Arvanitis-Vigneault, Devisree Valsakumar and 9 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. DDM1 Maintains Heterochromatin by Regulating Histone Variants.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Article
  11. TONSL promotes lung adenocarcinoma progression, immune escape and drug sensitivity.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Hossein Davarinejad *Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada.ORCID 0000-0002-6049-1492
Yi-Chun Huang *Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0002-7487-4443
Benoit MermazDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0002-2573-4401
Chantal LeBlancDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0003-1173-3579
Axel PouletDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0002-3415-8960
Geoffrey ThomsonDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0003-0848-1550
Valentin JolyDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0001-9357-764X
Marcelo MuñozWellcome Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, UK.ORCID 0000-0001-7748-4996
Alexis Arvanitis-VigneaultOttawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada.ORCID 0000-0002-3652-7467
Devisree ValsakumarBEaTS Research Laboratory, Division of Cardiac Surgery, University of Ottawa Heart Institute, Ottawa, Ontario K1Y 4W7, Canada.ORCID 0000-0002-8279-6369
Gonzalo VillarinoDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0003-2832-6785
Alex RossWellcome Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, UK.ORCID 0000-0001-8013-4858
Benjamin H RotsteinEpigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK.ORCID 0000-0001-9707-9357
Emilio I AlarconWellcome Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, UK.
Joseph S BrunzelleDepartment of Molecular Pharmacology and Biological Chemistry, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0001-9197-0018
Philipp VoigtBEaTS Research Laboratory, Division of Cardiac Surgery, University of Ottawa Heart Institute, Ottawa, Ontario K1Y 4W7, Canada.ORCID 0000-0003-4366-0490
Jie DongDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0003-0493-1665
Jean-François CoutureOttawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada.ORCID 0000-0003-0385-4450
Yannick JacobDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.ORCID 0000-0003-4741-0755

Funding

Understanding the roles of histone H3 variants in promoting genomic and epigenomic stability during DNA replication and agingR35GM128661 · NIGMS · YALE UNIVERSITY · PI YANNICK JACOB · 2018 to 2026
$4.0M
NIGMS NIH HHS R35 GM128661
6 · The paper itself

Abstract

The tail of replication-dependent histone H3.1 varies from that of replication-independent H3.3 at the amino acid located at position 31 in plants and animals, but no function has been assigned to this residue to demonstrate a unique and conserved role for H3.1 during replication. We found that TONSOKU (TSK/TONSL), which rescues broken replication forks, specifically interacts with H3.1 via recognition of alanine 31 by its tetratricopeptide repeat domain. Our results indicate that genomic instability in the absence of ATXR5/ATXR6-catalyzed histone H3 lysine 27 monomethylation in plants depends on H3.1, TSK, and DNA polymerase theta (Pol θ). This work reveals an H3.1-specific function during replication and a common strategy used in multicellular eukaryotes for regulating post-replicative chromatin maturation and TSK, which relies on histone monomethyltransferases and reading of the H3.1 variant.

Indexed as

DNA RepairDNA ReplicationArabidopsisArabidopsis ProteinsDNA Breaks, Double-StrandedDNA-Directed DNA PolymeraseDNA, PlantDNA Polymerase thetaGenome, PlantGenomic InstabilityHistonesLysineMethylationMethyltransferasesMutationProtein Interaction Domains and MotifsArabidopsis ProteinsATXR5 protein, ArabidopsisATXR6 protein, ArabidopsisDNA-Directed DNA PolymeraseDNA, PlantDNA Polymerase thetaHistonesLysineMethyltransferases

Identifiers

PMID35298257
PMCPMC9153895

What OpenQuestion holds

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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.