Evidence map›Paper›PMID 35951744›Full record

ArticleGenetics2022

TOP-2 is differentially required for the proper maintenance of the cohesin subunit REC-8 on meiotic chromosomes in Caenorhabditis elegans spermatogenesis and oogenesis.

Christine Rourke, Aimee Jaramillo-Lambert

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. bioRxiv : the preprint server for biology · 2026
    Article
  3. 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

2 authors at 1 institution in 1 country.

Christine RourkeDepartment of Biological Sciences, University of Delaware, Newark, DE 19716, USA.ORCID 0000-0002-4585-657X
Aimee Jaramillo-LambertDepartment of Biological Sciences, University of Delaware, Newark, DE 19716, USA.ORCID 0000-0001-7697-8580
University of Delaware · US

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI MELINDA K DUNCAN · 2012 to 2026
$67.2M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Chemistry-Biology Interface Predoctoral Training Grant 2024-2029T32GM133395 · NIGMS · UNIVERSITY OF DELAWARE · PI Catherine Leimkuhler Grimes · 2019 to 2026
$3.7M
New roles for Topoisomerase II in meiosisR35GM142524 · NIGMS · UNIVERSITY OF DELAWARE · PI JARAMILLO-LAMBERT, AIMEE · 2021 to 2025
$2.0M
Zeiss LSM710 Inverted Confocal MicroscopeS10OD016361 · OD · UNIVERSITY OF DELAWARE · PI CAPLAN, JEFFREY L · 2015 to 2015
$444k
Elucidating a new function for Topoisomerase II in meiotic chromosome segregationR03HD098244 · NICHD · UNIVERSITY OF DELAWARE · PI JARAMILLO-LAMBERT, AIMEE · 2019 to 2020
$152k
NICHD NIH HHS R03 HD098244NIGMS NIH HHS P20 GM103446NIGMS NIH HHS R35 GM142524NIGMS NIH HHS T32 GM133395NIH HHS S10 OD016361
6 · The paper itself

Abstract

During meiotic prophase I, accurate segregation of homologous chromosomes requires the establishment of chromosomes with a meiosis-specific architecture. The sister chromatid cohesin complex and the enzyme Topoisomerase II (TOP-2) are important components of meiotic chromosome architecture, but the relationship of these proteins in the context of meiotic chromosome segregation is poorly defined. Here, we analyzed the role of TOP-2 in the timely release of the sister chromatid cohesin subunit REC-8 during spermatogenesis and oogenesis of Caenorhabditis elegans. We show that there is a different requirement for TOP-2 in meiosis of spermatogenesis and oogenesis. The loss-of-function mutation top-2(it7) results in premature REC-8 removal in spermatogenesis, but not oogenesis. This correlates with a failure to maintain the HORMA-domain proteins HTP-1 and HTP-2 (HTP-1/2) on chromosome axes at diakinesis and mislocalization of the downstream components that control REC-8 release including Aurora B kinase. In oogenesis, top-2(it7) causes a delay in the localization of Aurora B to oocyte chromosomes but can be rescued through premature activation of the maturation promoting factor via knockdown of the inhibitor kinase WEE-1.3. The delay in Aurora B localization is associated with an increase in the length of diakinesis bivalents and wee-1.3 RNAi mediated rescue of Aurora B localization in top-2(it7) is associated with a decrease in diakinesis bivalent length. Our results imply that the sex-specific effects of TOP-2 on REC-8 release are due to differences in the temporal regulation of meiosis and chromosome structure in late prophase I in spermatogenesis and oogenesis.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsAnimalsAurora Kinase BCell Cycle ProteinsChromatidsChromosomal Proteins, Non-HistoneChromosomesChromosome SegregationCohesinsDNA Topoisomerases, Type IIFemaleMaleMaturation-Promoting FactorMeiosisProtein Serine-Threonine KinasesAurora Kinase BCaenorhabditis elegans ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsDNA Topoisomerases, Type IIHtp-1 protein, C elegansMaturation-Promoting FactorProtein Serine-Threonine KinasesProtein-Tyrosine Kinaseswee-1.3 protein, C elegansCaenorhabditis eleganschromosome segregationmeiosisREC-8TOP-2topoisomerase II

Identifiers

PMID35951744
PMCPMC9526062
OpenAlexW4293298769

What OpenQuestion holds

Textmetadata
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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.