Evidence map›Paper›PMID 42830301›Full record

ArticleNature communications2026

Molecular basis of nick ligation in the nucleosome by DNA Ligase IIIα.

Daniel J Boesch, Nadia I Martin, Chantal A Kontor, Ashlee G Nguyen, Alan E Tomkinson, Bennett Van Houten, Natacha Gillet, Emmanuelle Bignon, Amy M Whitaker, Tyler M Weaver

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Daniel J Boesch *Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA.
Nadia I Martin *Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA.
Chantal A KontorCancer Epigenetics Institute, Nuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA, USA.
Ashlee G NguyenDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA.
Alan E TomkinsonDepartments of Internal Medicine, Molecular Genetics & Microbiology, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0000-0002-2671-1711
Bennett Van HoutenUPMC, Hillman Cancer Center, Pittsburgh, PA, USA.ORCID 0000-0002-4009-2478
Natacha GilletCNRS, ENS de Lyon, LCH, UMR 5182, Lyon cedex 07, France.
Emmanuelle BignonUniversité de Lorraine, CNRS, UMR 7019 LPCT, Nancy, France.
Amy M WhitakerCancer Epigenetics Institute, Nuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA, USA.
Tyler M WeaverDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA. fsp8ux@virginia.edu.ORCID 0000-0002-5138-7140

Funding

Transcription-Coupled & Replication-Associated Excision RepairP01CA092584 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI John A. Tainer · 2001 to 2026
$89.6M
Roles of LIG3 and XRCC1 genes in genome stability.R01ES012512 · NIEHS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Alan E Tomkinson · 2004 to 2026
$6.3M
Watching cooperative interactions between base and nucleotide excision repair proteinsR35ES031638 · NIEHS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Bennett Van Houten · 2020 to 2026
$6.2M
Interplay between DNA base excision repair and transcriptional regulationR35GM155098 · NIGMS · RESEARCH INST OF FOX CHASE CAN CTR · PI Amy Michelle Whitaker · 2024 to 2026
$1.4M
NCI NIH HHS P01 CA092584NIEHS NIH HHS R01 ES012512NIEHS NIH HHS R35 ES031638NIGMS NIH HHS R35 GM155098
6 · The paper itself

Abstract

Genomic DNA is packaged into chromatin through a fundamental repeating unit known as the nucleosome core particle. Chromatinized genomic DNA is constantly exposed to endogenous and exogenous stresses that result in DNA damage, which must be repaired to maintain genome stability. Single-strand breaks (SSBs) are a prevalent form of DNA damage that arise via the oxidation-induced disintegration of the sugar-phosphate backbone or as repair intermediates during base excision repair. DNA ligase IIIα (LigIIIα) is one of the primary enzymes responsible for repairing ligatable SSBs during the terminal step of single-strand break repair (SSBR) and base excision repair (BER). To date, a mechanistic description of how LigIIIα processes nicks within chromatin remains elusive. Here, we use a combination of biochemical assays, molecular dynamics simulations, and cryogenic electron microscopy to define the molecular basis of nick ligation in the nucleosome by LigIIIα, providing foundational insight into the terminal step of chromatin-based SSBR/BER.

Indexed as

DNA Breaks, Single-StrandedDNA Ligase ATPNucleosomesXenopus ProteinsAnimalsChromatinCryoelectron MicroscopyDNA DamageDNA RepairExcision RepairMolecular Dynamics SimulationPoly-ADP-Ribose Binding ProteinsXenopus laevisChromatinDNA Ligase ATPDNA ligase III alpha protein, XenopusNucleosomesPoly-ADP-Ribose Binding ProteinsXenopus Proteins

Identifiers

PMID42830301
PMCPMC13635136

What OpenQuestion holds

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Registered trials

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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.