Evidence map›Paper›PMID 17000766›Full record

ArticleMolecular and cellular biology2006

The Hsp90 cochaperone p23 is essential for perinatal survival.

Iwona Grad, Thomas A McKee, Sara M Ludwig, Gary W Hoyle, Patricia Ruiz, Wolfgang Wurst, Thomas Floss, Charles A Miller, Didier Picard

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular and cellular biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

46 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. General Structural and Functional Features of Molecular Chaperones.Advances in experimental medicine and biology · 2021
    Article
  8. Review
  9. The HSP90 chaperone machinery.Nature reviews. Molecular cell biology · 2017
    Review
  10. Review
  11. Prostaglandin terminal synthases as novel therapeutic targets.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
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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

9 authors at 4 institutions in 3 countries.

Iwona GradDépartement de Biologie Cellulaire, Université de Genève, Sciences III, 1211 Genève 4, Switzerland. picard@cellbio.unige.ch
Thomas A McKee
Sara M Ludwig
Gary W Hoyle
Patricia Ruiz
Wolfgang Wurst
Thomas Floss
Charles A Miller
Didier Picard
Max Planck Institute for Molecular Genetics · DEInstitute of Groundwater Ecology · DETulane University · USUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The functions of molecular chaperones have been extensively investigated biochemically in vitro and genetically in bacteria and yeast. We have embarked on a functional genomic analysis of the Hsp90 chaperone machine in the mouse by disrupting the p23 gene using a gene trap approach. p23 is an Hsp90 cochaperone that is thought to stabilize Hsp90-substrate complexes and, independently, to act as the cytosolic prostaglandin E2 synthase. Gene deletions in budding and fission yeasts and knock-down experiments with the worm have not revealed any clear in vivo requirements for p23. We find that p23 is not essential for overall prenatal development and morphogenesis of the mouse, which parallels the observation that it is dispensable for proliferation in yeast. In contrast, p23 is absolutely necessary for perinatal survival. Apart from an incompletely formed skin barrier, the lungs of p23 null embryos display underdeveloped airspaces and substantially reduced expression of surfactant genes. Correlating with the known function of glucocorticoids in promoting lung maturation and the role of p23 in the assembly of a hormone-responsive glucocorticoid receptor-Hsp90 complex, p23 null fibroblast cells have a defective glucocorticoid response. Thus, p23 contributes a nonredundant, temporally restricted, and tissue-specific function during mouse development.

Indexed as

Animals, NewbornAnimalsCell Line, TransformedCell Transformation, ViralFibroblastsGene DeletionHSP90 Heat-Shock ProteinsIntramolecular OxidoreductasesLungMiceMice, KnockoutMice, Mutant StrainsMolecular ChaperonesMutagenesis, InsertionalPhosphoproteinsProstaglandin-E SynthasesHSP90 Heat-Shock ProteinsIntramolecular OxidoreductasesMolecular ChaperonesPhosphoproteinsProstaglandin-E SynthasesPtges3 protein, mouseReceptors, Glucocorticoid

Identifiers

PMID17000766
PMCPMC1636834
OpenAlexW2159065117

What OpenQuestion holds

Textmetadata
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.