Evidence map›Paper›PMID 25340700›Full record

ArticlePLoS genetics2014

It's all in your mind: determining germ cell fate by neuronal IRE-1 in C. elegans.

Mor Levi-Ferber, Yehuda Salzberg, Modi Safra, Anat Haviv-Chesner, Hannes E Bülow, Sivan Henis-Korenblit

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 22% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  4. Neuronal IL-17 controlsProceedings of the National Academy of Sciences of the United States of America · 2024
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  8. TFG regulates secretory and endosomal sorting pathways in neurons to promote their activity and maintenance.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Neuronal regulatedeLife · 2021
    Article
  11. Inactivation of theAutophagy · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Protein Quality Control in Health and Disease.Cold Spring Harbor perspectives in biology · 2017
    Review
  18. Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Mor Levi-FerberThe Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
Yehuda SalzbergDepartment of Genetics, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, New York, United States of America.
Modi SafraThe Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
Anat Haviv-ChesnerThe Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
Hannes E BülowDepartment of Genetics, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, New York, United States of America.
Sivan Henis-KorenblitThe Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
Bar-Ilan University · ILAlbert Einstein College of Medicine · US

Funding

Establishing the Role of a Novel Conserved Gene in Dendrite MorphogenesisR21NS081505 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BUELOW, HANNES ERICH · 2013 to 2014
$457k
NINDS NIH HHS R21 NS081505
6 · The paper itself

Abstract

The C. elegans germline is pluripotent and mitotic, similar to self-renewing mammalian tissues. Apoptosis is triggered as part of the normal oogenesis program, and is increased in response to various stresses. Here, we examined the effect of endoplasmic reticulum (ER) stress on apoptosis in the C. elegans germline. We demonstrate that pharmacological or genetic induction of ER stress enhances germline apoptosis. This process is mediated by the ER stress response sensor IRE-1, but is independent of its canonical downstream target XBP-1. We further demonstrate that ire-1-dependent apoptosis in the germline requires both CEP-1/p53 and the same canonical apoptotic genes as DNA damage-induced germline apoptosis. Strikingly, we find that activation of ire-1, specifically in the ASI neurons, but not in germ cells, is sufficient to induce apoptosis in the germline. This implies that ER stress related germline apoptosis can be determined at the organism level, and is a result of active IRE-1 signaling in neurons. Altogether, our findings uncover ire-1 as a novel cell non-autonomous regulator of germ cell apoptosis, linking ER homeostasis in sensory neurons and germ cell fate.

Indexed as

Signal TransductionAnimalsApoptosisCaenorhabditis elegansCaenorhabditis elegans ProteinsCarrier ProteinsCell DifferentiationDNA DamageEndoplasmic Reticulum StressGerm CellsGonadsNeuronsProtein Serine-Threonine KinasesCaenorhabditis elegans ProteinsCarrier ProteinsIRE-1 protein, C elegansProtein Serine-Threonine KinasesXBP-1 protein, C elegans

Identifiers

PMID25340700
PMCPMC4207656
OpenAlexW1964730983

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.