Evidence map›Paper›PMID 41379861›Full record

ArticlePLoS genetics2025

The conserved SEN1 DNA/RNA helicase has multiple functions during yeast meiosis.

Robert Gaglione, Leonidas Pierrakeas, Lihong Wan, Jonathan Caradonna, Amy J MacQueen, Ed Luk, Nancy M Hollingsworth

Abstract read
In one paragraph

Article in PLoS genetics, 2025. 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. bioRxiv : the preprint server for biology · 2026
    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

7 authors.

Robert GaglioneDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.ORCID https://orcid.org/0000-0002-4126-5887
Leonidas PierrakeasDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.
Lihong WanDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.
Jonathan CaradonnaDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.ORCID https://orcid.org/0009-0003-8438-5402
Amy J MacQueenDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, Connecticut, United States of America.ORCID https://orcid.org/0000-0002-0919-7538
Ed LukDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.ORCID https://orcid.org/0000-0002-6619-2258
Nancy M HollingsworthDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.ORCID https://orcid.org/0000-0003-3300-6444

Funding

Meiotic recombination in budding yeastR35GM140684 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI HOLLINGSWORTH, NANCY M. · 2021 to 2025
$2.1M
How Do Synaptonemal Complex Proteins Promote Crossover Recombination and Synapsis?R15GM116109 · NIGMS · WESLEYAN UNIVERSITY · PI MACQUEEN, AMY JOY · 2016 to 2025
$2.1M
Variant Chromatin Structures-Targeting and FunctionsR35GM156364 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI Edward E Luk · 2025 to 2026
$1.1M
NIGMS NIH HHS R15 GM116109NIGMS NIH HHS R35 GM140684NIGMS NIH HHS R35 GM156364
6 · The paper itself

Abstract

dnaRNA hybrids are unusual structures found throughout the genomes of many species, including yeast and mammals. While DNA:RNA hybrids may promote various cellular functions, persistent hybrids lead to double strand breaks, resulting in genomic instability. DNA:RNA hybrid formation and removal are therefore highly regulated, including by enzymes that either degrade or unwind RNA from the hybrid. Meiosis is the specialized cell division that creates haploid gametes for sexual reproduction. Previous work in yeast and mammals showed that elimination of DNA:RNA hybrids by RNase H facilitates meiotic recombination. This work demonstrates that the conserved Sen1 DNA/RNA helicase functions during three temporally distinct processes during yeast meiosis. First, SEN1 allows meiosis-specific genes to be expressed at the proper time to allow entry into meiosis. Second, SEN1 prevents the accumulation of hybrids during premeiotic DNA replication. Third, SEN1 promotes the repair of programmed meiotic double strand breaks that are necessary to form crossovers between homologous chromosomes to allow their proper segregation at the first meiotic division. Given the evolutionary conservation of Sen1 with its mammalian counterpart, Senataxin, studies of Sen1 function in yeast are likely to be informative about the regulation of DNA:RNA hybrids during human meiosis as well.

Indexed as

DNA HelicasesMeiosisRNA HelicasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsDNA Breaks, Double-StrandedDNA RepairDNA ReplicationGenomic InstabilityDNA HelicasesRNA HelicasesSaccharomyces cerevisiae ProteinsSEN1 protein, S cerevisiae

Identifiers

PMID41379861
PMCPMC12714266

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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.