Evidence map›Paper›PMID 9199334›Full record

ArticleMolecular and cellular biology1997

Nuclear receptor steroidogenic factor 1 directs embryonic stem cells toward the steroidogenic lineage.

P A Crawford, Y Sadovsky, J Milbrandt

Open access · hybridAbstract read
In one paragraph

Article in Molecular and cellular biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

47 citing papers in PubMed, 134 citations in OpenAlex.

  1. Adrenocortical stem cells in health and disease.Nature reviews. Endocrinology · 2025
    Review
  2. Article
  3. Article
  4. Fetal Leydig cells: What we know and what we don't.Molecular reproduction and development · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Embryonic Development and Adult Regeneration of the Adrenal Gland.Endocrinology and metabolism (Seoul, Korea) · 2020
    Review
  14. Coordination of Multiple Cellular Processes by NR5A1/Nr5a1.Endocrinology and metabolism (Seoul, Korea) · 2020
    Review
  15. Article
  16. 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

3 authors at 1 institution in 1 country.

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

Funding

NCPDCID CDC HHS NCI 49712-07
6 · The paper itself

Abstract

The orphan nuclear receptor steroidogenic factor 1 (SF-1) is expressed in the adrenal gland and gonads and is an important regulator of the expression of cytochrome P-450 steroidogenic enzymes in cultured cells. Targeted disruption of the SF-1 gene in mice shows that it is a critical participant in the genetic program that promotes the development of urogenital mesoderm into the adrenal gland and gonads. To assess the ability of SF-1 to regulate this differentiation pathway, we ectopically expressed SF-1 in murine embryonic stem (ES) cells. We found that stable expression of SF-1 is sufficient to alter ES cell morphology, permit cyclic AMP (cAMP) and retinoic acid-induced expression of the endogenous side chain cleavage enzyme gene, and consequently, promote steroidogenesis. While steroid production is dependent upon SF-1, cAMP induction of steroidogenesis does not enhance the responsiveness of an SF-1-specific reporter. Furthermore, the activity of a P450SCC promoter/luciferase reporter construct, which is induced by cAMP in steroidogenic cells and ES cells converted by stable expression of SF-1, is not induced by cAMP in wild-type ES cells transiently transfected with SF-1, suggesting that the induction of downstream gene products is required before steroidogenesis can occur. We demonstrate that mutants which disrupt the DNA binding domain or the AF2 transcriptional activation domain of SF-1 do not confer the steroidogenic phenotype to ES cells. Interestingly, however, AF2 mutants fused to the VP16 activation domain do confer the steroidogenic phenotype to ES cells, but only in the presence of a portion of the ligand binding domain. These studies extend the role of SF-1 in steroidogenic tissues to that of a dominant regulator of the steroidogenic cell phenotype.

Indexed as

Gene Expression Regulation, DevelopmentalAdrenal GlandsAnimalsBinding SitesCell DifferentiationCholesterol Side-Chain Cleavage EnzymeCyclic AMPDNA-Binding ProteinsEmbryo, MammalianFushi Tarazu Transcription FactorsGonadsHomeodomain ProteinsMiceProgesteroneReceptors, Cytoplasmic and NuclearStem CellsCholesterol Side-Chain Cleavage EnzymeCyclic AMPDNA-Binding ProteinsFushi Tarazu Transcription FactorsHomeodomain ProteinsProgesteroneReceptors, Cytoplasmic and NuclearSteroidogenic Factor 1steroidogenic factor 1, mouseTranscription FactorsTretinoin

Identifiers

PMID9199334
PMCPMC232252
OpenAlexW2111924561

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.