Evidence map›Paper›PMID 22185090›Full record

ArticleGenome biology2011

Caenorhabditis elegans Heterochromatin protein 1 (HPL-2) links developmental plasticity, longevity and lipid metabolism.

Peter Meister, Sonia Schott, Cécile Bedet, Yu Xiao, Sabine Rohner, Selena Bodennec, Bruno Hudry, Laurent Molin, Florence Solari, Susan M Gasser and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

24 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. mMolecular biology reports · 2023
    Article
  6. Article
  7. Chromatin: the old and young of it.Frontiers in molecular biosciences · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Repressive Chromatin inGenetics · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 5 institutions in 2 countries.

Peter MeisterLaboratory of Molecular and Cellular Biology, CNRS, Université de Lyon, Ecole Normale Supérieure, Lyon Cedex 07, France.
Sonia Schott
Cécile Bedet
Yu Xiao
Sabine Rohner
Selena Bodennec
Bruno Hudry
Laurent Molin
Florence Solari
Susan M Gasser
Francesca Palladino
École Normale Supérieure de Lyon · FRFriedrich Miescher Institute · CHCentre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FRInstitut de Biologie du Développement Marseille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeterochromatin protein 1 (HP1) family proteins have a well-characterized role in heterochromatin packaging and gene regulation. Their function in organismal development, however, is less well understood. Here we used genome-wide expression profiling to assess novel functions of the Caenorhabditis elegans HP1 homolog HPL-2 at specific developmental stages.

resultsWe show that HPL-2 regulates the expression of germline genes, extracellular matrix components and genes involved in lipid metabolism. Comparison of our expression data with HPL-2 ChIP-on-chip profiles reveals that a significant number of genes up- and down-regulated in the absence of HPL-2 are bound by HPL-2. Germline genes are specifically up-regulated in hpl-2 mutants, consistent with the function of HPL-2 as a repressor of ectopic germ cell fate. In addition, microarray results and phenotypic analysis suggest that HPL-2 regulates the dauer developmental decision, a striking example of phenotypic plasticity in which environmental conditions determine developmental fate. HPL-2 acts in dauer at least partly through modulation of daf-2/IIS and TGF-β signaling pathways, major determinants of the dauer program. hpl-2 mutants also show increased longevity and altered lipid metabolism, hallmarks of the long-lived, stress resistant dauers.

conclusionsOur results suggest that the worm HP1 homologue HPL-2 may coordinately regulate dauer diapause, longevity and lipid metabolism, three processes dependent on developmental input and environmental conditions. Our findings are of general interest as a paradigm of how chromatin factors can both stabilize development by buffering environmental variation, and guide the organism through remodeling events that require plasticity of cell fate regulation.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsChromosomal Proteins, Non-HistoneEnvironmentGene Expression ProfilingGerm CellsHermaphroditic OrganismsHeterochromatinLipid MetabolismLongevityMaleMutationOligonucleotide Array Sequence AnalysisReceptor, InsulinCaenorhabditis elegans ProteinsChromosomal Proteins, Non-HistoneDAF-2 protein, C elegansHeterochromatinHPL-2 protein, C elegansReceptor, InsulinRepressor ProteinsTransforming Growth Factor beta

Identifiers

PMID22185090
PMCPMC3334618
OpenAlexW2069753975

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.