Evidence map›Paper›PMID 9566914›Full record

ArticleMolecular and cellular biology1998

Nuclear receptor DAX-1 recruits nuclear receptor corepressor N-CoR to steroidogenic factor 1.

P A Crawford, C Dorn, Y Sadovsky, J Milbrandt

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
19.5field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 339 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Case Report: A Novel Truncating Variant ofFrontiers in endocrinology · 2022
    Article
  6. Adrenal cortex renewal in health and disease.Nature reviews. Endocrinology · 2021
    Review
  7. Article
  8. Article
  9. The nuclear receptor superfamily: A structural perspective.Protein science : a publication of the Protein Society · 2018
    Review
  10. Article
  11. Regulation of PXR and CAR by protein-protein interaction and signaling crosstalk.Expert opinion on drug metabolism & toxicology · 2016
    Review
  12. TNF-α-mediated suppression of Leydig cell steroidogenesis involves DAX-1.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2015
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Nuclear receptor corepressor complexes in cancer: mechanism, function and regulation.American journal of clinical and experimental urology · 2014
    Review
  18. Article
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

P A CrawfordDepartment of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
C Dorn
Y Sadovsky
J Milbrandt
Washington University in St. Louis · US

Funding

ACTIVATION FUNCTION OF STEROIDOGENIC FACTOR 1R29HD034110 · NICHD · WASHINGTON UNIVERSITY · PI SADOVSKY, YOEL · 1997 to 2001
$218k
NICHD NIH HHS HD-34110PHS HHS P01-49712-07
6 · The paper itself

Abstract

The orphan nuclear receptor steroidogenic factor 1 (SF-1) is a critical developmental regulator in the urogenital ridge, because mice targeted for disruption of the SF-1 gene lack adrenal glands and gonads. SF-1 was recently shown to interact with DAX-1, another orphan receptor whose tissue distribution overlaps that of SF-1. Naturally occurring loss-of-function mutations of the DAX-1 gene cause the human disorder X-linked adrenal hypoplasia congenita (AHC), which resembles the phenotype of SF-1-deficient mice. Paradoxically, however, DAX-1 represses the transcriptional activity of SF-1, and AHC mutants of DAX-1 lose repression function. To further investigate these findings, we characterized the interaction between SF-1 and DAX-1 and found that their interaction indeed occurs through a repressive domain within the carboxy terminus of SF-1. Furthermore, we demonstrate that DAX-1 recruits the nuclear receptor corepressor N-CoR to SF-1, whereas naturally occurring AHC mutations of DAX-1 permit the SF-1-DAX-1 interaction, but markedly diminish corepressor recruitment. Finally, the interaction between DAX-1 and N-CoR shares similarities with that of the nuclear receptor RevErb and N-CoR, because the related corepressor SMRT was not efficiently recruited by DAX-1. Therefore, DAX-1 can serve as an adapter molecule that recruits nuclear receptor corepressors to DNA-bound nuclear receptors like SF-1, thereby extending the range of corepressor action.

Indexed as

Adrenal Gland DiseasesAmino Acid SequenceAnimalsBinding SitesConserved SequenceDAX-1 Orphan Nuclear ReceptorDNA-Binding ProteinsFushi Tarazu Transcription FactorsGene Expression Regulation, DevelopmentalGenetic LinkageHomeodomain ProteinsHumansMiceModels, GeneticMolecular Sequence DataNuclear ProteinsDAX-1 Orphan Nuclear ReceptorDNA-Binding ProteinsFushi Tarazu Transcription FactorsHomeodomain ProteinsNCOR1 protein, humanNcor1 protein, mouseNR0B1 protein, humanNr0b1 protein, mouseNR5A1 protein, humanNuclear ProteinsNuclear Receptor Co-Repressor 1Receptors, Cytoplasmic and NuclearReceptors, Retinoic AcidRepressor ProteinsSteroidogenic Factor 1steroidogenic factor 1, mouseTranscription Factors

Identifiers

PMID9566914
PMCPMC110674
OpenAlexW1798563091

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.