Evidence map›Paper›PMID 30024879›Full record

ArticlePLoS genetics2018

Binucleate germ cells in Caenorhabditis elegans are removed by physiological apoptosis.

Stephan A Raiders, Michael D Eastwood, Meghan Bacher, James R Priess

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

50 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Expanding thebioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Apoptosis promotes fertility inbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Mitochondrial curation for the next generation.Current opinion in genetics & development · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Stephan A RaidersFred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Michael D EastwoodFred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Meghan BacherFred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
James R PriessFred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.ORCID 0000-0002-4087-7419
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Mechanisms of epithelial remodeling during organ development in C. elegansR01GM098583 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRIESS, JAMES R · 2011 to 2020
$4.0M
The role of the cytoskeleton in germ cell apoptosis in C. elegansR01GM107474 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRIESS, JAMES R · 2013 to 2016
$1.3M
NIGMS NIH HHS R01 GM098583NIGMS NIH HHS R01 GM107474NIH HHS P40 OD010440
6 · The paper itself

Abstract

Cell death plays a major role during C. elegans oogenesis, where over half of the oogenic germ cells die in a process termed physiological apoptosis. How germ cells are selected for physiological apoptosis, or instead become oocytes, is not understood. Most oocytes produce viable embryos when apoptosis is blocked, suggesting that physiological apoptosis does not function to cull defective germ cells. Instead, cells targeted for apoptosis may function as nurse cells; the germline is syncytial, and all germ cells appear to contribute cytoplasm to developing oocytes. C. elegans has been a leading model for the genetics and molecular biology of apoptosis and phagocytosis, but comparatively few studies have examined the cell biology of apoptotic cells. We used live imaging to identify and examine pre-apoptotic germ cells in the adult gonad. After initiating apoptosis, germ cells selectively export their mitochondria into the shared pool of syncytial cytoplasm; this transport appears to use the microtubule motor kinesin. The apoptotic cells then shrink as they expel most of their remaining cytoplasm, and close off from the syncytium. Shortly thereafter the apoptotic cells restructure their microtubule and actin cytoskeletons, possibly to maintain cell integrity; the microtubules form a novel, cortical array of stabilized microtubules, and actin and cofilin organize into giant cofilin-actin rods. We discovered that some apoptotic germ cells are binucleate; the binucleate germ cells can develop into binucleate oocytes in apoptosis-defective strains, and appear capable of producing triploid offspring. Our results suggest that the nuclear layer of the germline syncytium becomes folded during mitosis and growth, and that binucleate cells arise as the layer unfolds or everts; all of the binucleate cells are subsequently removed by apoptosis. These results show that physiological apoptosis targets at least two distinct populations of germ cells, and that the apoptosis machinery efficiently recognizes cells with two nuclei.

Indexed as

AnimalsAnimals, Genetically ModifiedApoptosisCaenorhabditis elegansCaenorhabditis elegans ProteinsCaspasesCell NucleusCytoplasmFemaleGerm CellsMaleMicrotubulesOocytesOogenesisOvaryCaenorhabditis elegans ProteinsCaspasesced-3 protein, C elegans

Identifiers

PMID30024879
PMCPMC6053125
OpenAlexW2883747051

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.