Evidence map›Paper›PMID 29608173›Full record

ArticleJournal of visualized experiments : JoVE2018

Manipulation of Ploidy in Caenorhabditis elegans.

Erlyana K Clarke, Katherine A Rivera Gomez, Zaki Mustachi, Mikaela C Murph, Mara Schvarzstein

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 59% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Identification of a new allele ofmicroPublication biology · 2025
    Article
  3. First comparative proteomic andFrontiers in veterinary science · 2025
    Article
  4. Invertebrate genetic models of amyotrophic lateral sclerosis.Frontiers in molecular neuroscience · 2024
    Review
  5. Article
  6. Review
  7. 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

5 authors at 3 institutions in 1 country.

Erlyana K ClarkeBrooklyn College, Biology Department, City University of New York.
Katherine A Rivera GomezBrooklyn College, Biology Department, City University of New York; The Graduate Center, Biology Department, City University of New York.
Zaki MustachiBrooklyn College, Biology Department, City University of New York.
Mikaela C MurphBrooklyn College, Biology Department, City University of New York; Advanced Science Research Center, City University of New York.
Mara SchvarzsteinBrooklyn College, Biology Department, City University of New York; The Graduate Center, Biology Department, City University of New York; Advanced Science Research Center, City University of New York; maraschvarzstein@gmail.com.
City University of New York · USBrooklyn College · USThe Graduate Center, CUNY · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
RISE Option 2:Increasing URM Student Success in Science and Science CareersR25GM062981 · NIGMS · BROOKLYN COLLEGE · PI HAINLINE, LOUISE · 2003 to 2015
$4.8M
Regulation of Chromosome and Centrosome Inheritance by HORMA Proteins in MeiosisSC2GM118275 · NIGMS · BROOKLYN COLLEGE · PI SCHVARZSTEIN, MARA · 2016 to 2018
$471k
NIGMS NIH HHS R25 GM062981NIGMS NIH HHS SC2 GM118275NIH HHS P40 OD010440
6 · The paper itself

Abstract

Mechanisms that involve whole genome polyploidy play important roles in development and evolution; also, an abnormal generation of tetraploid cells has been associated with both the progression of cancer and the development of drug resistance. Until now, it has not been feasible to easily manipulate the ploidy of a multicellular animal without generating mostly sterile progeny. Presented here is a simple and rapid protocol for generating tetraploid Caenorhabditis elegans animals from any diploid strain. This method allows the user to create a bias in chromosome segregation during meiosis, ultimately increasing ploidy in C. elegans. This strategy relies on the transient reduction of expression of the rec-8 gene to generate diploid gametes. A rec-8 mutant produces diploid gametes that can potentially produce tetraploids upon fertilization. This tractable scheme has been used to generate tetraploid strains carrying mutations and chromosome rearrangements to gain insight into chromosomal dynamics and interactions during pairing and synapsis in meiosis. This method is efficient for generating stable tetraploid strains without genetic markers, can be applied to any diploid strain, and can be used to derive triploid C. elegans. This straightforward method is useful for investigating other fundamental biological questions relevant to genome instability, gene dosage, biological scaling, extracellular signaling, adaptation to stress, development of resistance to drugs, and mechanisms of speciation.

Indexed as

PloidiesAnimalsCaenorhabditis elegansMale

Identifiers

PMID29608173
PMCPMC5931776
OpenAlexW2791421914

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.