Evidence map›Paper›PMID 24316205›Full record

ArticleCurrent biology : CB2013

The unfolded protein response in a pair of sensory neurons promotes entry of C. elegans into dauer diapause.

Warakorn Kulalert, Dennis H Kim

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

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  10. ENPL-1, theDevelopment (Cambridge, England) · 2020
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  12. Ascaroside Pheromones: Chemical Biology and Pleiotropic Neuronal Functions.International journal of molecular sciences · 2019
    Review
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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

2 authors at 1 institution in 1 country.

Warakorn KulalertDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Dennis H KimDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA. Electronic address: dhkim@mit.edu.
Massachusetts Institute of Technology · US

Funding

Molecular Genetics of Innate Immunity in C. elegansR01GM084477 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KIM, DENNIS H · 2007 to 2020
$4.6M
NIGMS NIH HHS GM084477NIGMS NIH HHS R01 GM084477
6 · The paper itself

Abstract

In response to unfavorable environmental conditions such as starvation, crowding, and elevated temperature, Caenorhabditis elegans larvae enter an alternative developmental stage known as dauer, which is characterized by adaptive changes in stress resistance and metabolism. The genetic dissection of the molecular mechanisms of the C. elegans dauer developmental decision has defined evolutionarily conserved signaling pathways of organismal neuroendocrine physiology. Here, we have identified a mechanism by which a dominant mutation in a neuronal insulin gene, daf-28(sa191), causes constitutive entry into dauer diapause. We demonstrate that expression of the mutant DAF-28 insulin peptide results in endoplasmic reticulum (ER) stress in the ASI pair of chemosensory neurons. The neuronal ER stress does not compromise cellular survival but activates PEK-1, the C. elegans ortholog of the mammalian eIF2α kinase PERK, which in turn phosphorylates Ser49 of eIF2α, specifically in the ASI neuron pair, to promote entry into dauer diapause. Our data establish a novel role for ER stress and the unfolded protein response (UPR) in promoting entry into dauer diapause and suggest that, in addition to cell-autonomous activities in the maintenance of ER homeostasis, the UPR may act in a non-cell-autonomous manner to promote organismal adaptation to stress during larval development.

Indexed as

Endoplasmic Reticulum StressUnfolded Protein ResponseAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Cycle ProteinsEukaryotic Initiation Factor-2Gene Expression Regulation, DevelopmentalHomeostasisInsulinsMAP Kinase Kinase 1MutationPhosphorylationReceptor, InsulinSensory Receptor CellsCaenorhabditis elegans ProteinsCell Cycle Proteinsdaf-28 protein, C elegansEukaryotic Initiation Factor-2InsulinsMAP Kinase Kinase 1pek-1 protein, C elegansReceptor, Insulin

Identifiers

PMID24316205
PMCPMC3870035
OpenAlexW2058925751

What OpenQuestion holds

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LicenceTDM
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.