Evidence map›Paper›PMID 42323311›Full record

ArticleNature communications2026

Break-induced replication forms long mutable single-strand DNA during meiosis.

Jerzy M Twarowski, Juraj Kramara, Gabriel J Seuferer, Kelley A Renninger, Josep M Comeron, Anna Malkova

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Jerzy M TwarowskiDepartment of Biology, University of Iowa, Iowa City, IA, USA.ORCID http://orcid.org/0000-0002-7180-1177
Juraj KramaraDepartment of Biology, University of Iowa, Iowa City, IA, USA.
Gabriel J SeufererDepartment of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Kelley A RenningerDepartment of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Josep M ComeronDepartment of Biology, University of Iowa, Iowa City, IA, USA.ORCID http://orcid.org/0000-0002-1256-6437
Anna MalkovaDepartment of Biology, University of Iowa, Iowa City, IA, USA. malkova@uthscsa.edu.ORCID http://orcid.org/0000-0002-3880-1781

Funding

Double strand break repair maelstrom: causes, mechanisms and genome destabilizing consequencesR35GM127006 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Anna L Malkova · 2018 to 2026
$3.8M
Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RR240030NIGMS NIH HHS R35 GM127006U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM127006
6 · The paper itself

Abstract

In meiosis, homologous recombination (HR) facilitates the halving of genomic content in diploid parents to produce haploid gametes, while also reshuffling genetic material. However, studies in yeast and mammals have suggested that HR during meiosis also makes the process mutagenic, and it has been proposed that the single-strand (ss) DNA formed by HR of programmed double-strand breaks (DSBs) contributes to the observed mutagenesis. To determine the full mutagenic potential of ssDNA formed during meiosis, we expressed human APOBEC3A (A3A), a deaminase that specifically attacks and therefore allows detection of ssDNA, in meiotic yeast cells. We demonstrate that meiotic cells accumulate long tracts of ssDNA manifested by A3A-mutation clusters, of up to 134 mutations spanning more than 25 kb. We show that the formation of mutation clusters during meiosis require Spo11-induced DSBs, and that break-induced replication and hyper-resection of DSBs are the primary mechanisms underlying the formation of long ssDNA. We also report meiotic ssDNA accumulation in promoters and tRNA genes, revealing them as additional sources of mutagenesis during meiosis. Together, our results demonstrate the high mutagenic potential of meiosis and provide insight into mechanisms that can fuel evolution and promote congenital diseases in humans.

Indexed as

DNA ReplicationDNA, Single-StrandedMeiosisCytidine DeaminaseDNA Breaks, Double-StrandedEndodeoxyribonucleasesHomologous RecombinationHumansMeiotic Recombination Protein SPO11MutagenesisMutationSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCytidine DeaminaseDNA, Single-StrandedEndodeoxyribonucleasesMeiotic Recombination Protein SPO11Saccharomyces cerevisiae ProteinsSpo11 protein, S cerevisiae

Identifiers

PMID42323311
PMCPMC13438675

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LicenceCC BY-NC-ND
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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.