Evidence map›Paper›PMID 36508468›Full record

ArticlePLoS genetics2022

Rad51-mediated interhomolog recombination during budding yeast meiosis is promoted by the meiotic recombination checkpoint and the conserved Pif1 helicase.

Andrew Ziesel, Qixuan Weng, Jasvinder S Ahuja, Abhishek Bhattacharya, Raunak Dutta, Evan Cheng, G Valentin Börner, Michael Lichten, Nancy M Hollingsworth

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. bioRxiv : the preprint server for biology · 2026
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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

9 authors at 3 institutions in 1 country.

Andrew ZieselBiochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.
Qixuan WengBiochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.
Jasvinder S AhujaLaboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States of America.
Abhishek BhattacharyaCenter for Gene Regulation in Health and Disease and Department of Biological, Geological and Environmental Sciences, Cleveland State University, Cleveland, Ohio, United States of America.
Raunak DuttaBiochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.
Evan ChengBiochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.
G Valentin BörnerCenter for Gene Regulation in Health and Disease and Department of Biological, Geological and Environmental Sciences, Cleveland State University, Cleveland, Ohio, United States of America.ORCID 0000-0001-6369-5119
Michael LichtenLaboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States of America.
Nancy M HollingsworthBiochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.ORCID 0000-0003-3300-6444
Stony Brook University · USCleveland State University · USNational Cancer Institute · US

Funding

ANALYSIS OF MEIOTIC CHROMOSOME SYNAPSIS IN YEASTR01GM050717 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI HOLLINGSWORTH, NANCY M. · 1995 to 2020
$8.0M
Role of Chromosomally Tethered Proteasome in Chromosome Pairing and Meiotic RecombinationR01GM125800 · NIGMS · CLEVELAND STATE UNIVERSITY · PI BOERNER, VALENTIN · 2018 to 2021
$2.3M
Meiotic recombination in budding yeastR35GM140684 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI HOLLINGSWORTH, NANCY M. · 2021 to 2025
$2.1M
Nikon A1RSI Confocal MicroscopeS10OD010381 · OD · CLEVELAND STATE UNIVERSITY · PI BARIK, SAILEN · 2012 to 2012
$591k
A Digital Laser Scanner Biomolecular Imaging System: Amersham Typhoon 5S10OD025252 · OD · CLEVELAND STATE UNIVERSITY · PI LI, BIBO · 2018 to 2018
$163k
NIGMS NIH HHS R01 GM050717NIGMS NIH HHS R01 GM125800NIGMS NIH HHS R35 GM140684NIH HHS S10 OD010381NIH HHS S10 OD025252
6 · The paper itself

Abstract

During meiosis, recombination between homologous chromosomes (homologs) generates crossovers that promote proper segregation at the first meiotic division. Recombination is initiated by Spo11-catalyzed DNA double strand breaks (DSBs). 5' end resection of the DSBs creates 3' single strand tails that two recombinases, Rad51 and Dmc1, bind to form presynaptic filaments that search for homology, mediate strand invasion and generate displacement loops (D-loops). D-loop processing then forms crossover and non-crossover recombinants. Meiotic recombination occurs in two temporally distinct phases. During Phase 1, Rad51 is inhibited and Dmc1 mediates the interhomolog recombination that promotes homolog synapsis. In Phase 2, Rad51 becomes active and functions with Rad54 to repair residual DSBs, making increasing use of sister chromatids. The transition from Phase 1 to Phase 2 is controlled by the meiotic recombination checkpoint through the meiosis-specific effector kinase Mek1. This work shows that constitutive activation of Rad51 in Phase 1 results in a subset of DSBs being repaired by a Rad51-mediated interhomolog recombination pathway that is distinct from that of Dmc1. Strand invasion intermediates generated by Rad51 require more time to be processed into recombinants, resulting in a meiotic recombination checkpoint delay in prophase I. Without the checkpoint, Rad51-generated intermediates are more likely to involve a sister chromatid, thereby increasing Meiosis I chromosome nondisjunction. This Rad51 interhomolog recombination pathway is specifically promoted by the conserved 5'-3' helicase PIF1 and its paralog, RRM3 and requires Pif1 helicase activity and its interaction with PCNA. This work demonstrates that (1) inhibition of Rad51 during Phase 1 is important to prevent competition with Dmc1 for DSB repair, (2) Rad51-mediated meiotic recombination intermediates are initially processed differently than those made by Dmc1, and (3) the meiotic recombination checkpoint provides time during prophase 1 for processing of Rad51-generated recombination intermediates.

Indexed as

DNA HelicasesMeiosisRad51 RecombinaseRecombination, GeneticSaccharomyces cerevisiae ProteinsCell Cycle ProteinsDNA-Binding ProteinsDNA RepairSaccharomyces cerevisiaeCell Cycle ProteinsDMC1 protein, S cerevisiaeDNA-Binding ProteinsDNA HelicasesPIF1 protein, S cerevisiaeRAD51 protein, S cerevisiaeRad51 RecombinaseRrm3 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID36508468
PMCPMC9779700
OpenAlexW4311180174

What OpenQuestion holds

Textmetadata
LicenceCC0
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.