Evidence map›Paper›PMID 36688410›Full record

ArticleThe EMBO journal2023

C. elegans molting requires rhythmic accumulation of the Grainyhead/LSF transcription factor GRH-1.

Milou W M Meeuse, Yannick P Hauser, Smita Nahar, A Alexander T Smith, Kathrin Braun, Chiara Azzi, Markus Rempfler, Helge Großhans

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2023. 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
2.4field-weighted citation impact, top 7% 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, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. A scheduler for rhythmic gene expression.Molecular systems biology · 2025
    Article
  6. Article
  7. A scheduler for rhythmic gene expression.bioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The NHR-23-regulated putative protease inhibitorbioRxiv : the preprint server for biology · 2024
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

8 authors at 2 institutions in 1 country.

Milou W M MeeuseFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0001-6382-6449
Yannick P HauserFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0003-1357-9712
Smita NaharFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0001-7449-9324
A Alexander T SmithFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0003-4593-3042
Kathrin BraunFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0003-1576-0486
Chiara AzziFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0002-2240-4618
Markus RempflerFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.
Helge GroßhansFriedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0002-8169-6905
Friedrich Miescher Institute · CHUniversity of Basel · CH

Funding

European Research Council 741269Marie Curie 842386Swiss National Science Foundation 310030_207470
6 · The paper itself

Abstract

C. elegans develops through four larval stages that are rhythmically terminated by molts, that is, the synthesis and shedding of a cuticular exoskeleton. Each larval cycle involves rhythmic accumulation of thousands of transcripts, which we show here relies on rhythmic transcription. To uncover the responsible gene regulatory networks (GRNs), we screened for transcription factors that promote progression through the larval stages and identified GRH-1, BLMP-1, NHR-23, NHR-25, MYRF-1, and BED-3. We further characterize GRH-1, a Grainyhead/LSF transcription factor, whose orthologues in other animals are key epithelial cell-fate regulators. We find that GRH-1 depletion extends molt durations, impairs cuticle integrity and shedding, and causes larval death. GRH-1 is required for, and accumulates prior to, each molt, and preferentially binds to the promoters of genes expressed during this time window. Binding to the promoters of additional genes identified in our screen furthermore suggests that we have identified components of a core molting-clock GRN. Since the mammalian orthologues of GRH-1, BLMP-1 and NHR-23, have been implicated in rhythmic homeostatic skin regeneration in mouse, the mechanisms underlying rhythmic C. elegans molting may apply beyond nematodes.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsAnimalsGene Expression Regulation, DevelopmentalMammalsMiceMoltingTranscription FactorsCaenorhabditis elegans ProteinsGRH-1 protein, C elegansTranscription Factorsdevelopmental clockgenetic oscillatorGrainyheadmoltingskin regeneration

Identifiers

PMID36688410
PMCPMC9929640
OpenAlexW4317746819

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.