Evidence map›Paper›PMID 19237537›Full record

ArticleMolecular and cellular biology2009

E3 ubiquitin ligase RNF31 cooperates with DAX-1 in transcriptional repression of steroidogenesis.

Anna Ehrlund, Elin Holter Anthonisen, Nina Gustafsson, Nicolas Venteclef, Kirsten Robertson Remen, Anastasios E Damdimopoulos, Anastasia Galeeva, Markku Pelto-Huikko, Enzo Lalli, Knut R Steffensen and 2 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. A Z-Linked E3 Ubiquitin LigaseAnimals : an open access journal from MDPI · 2021
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. RBR E3-ligases at work.EMBO reports · 2014
    Review
  16. Article
  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

12 authors at 4 institutions in 5 countries.

Anna EhrlundDepartment of Biosciences and Nutrition, Karolinska Institutet, S-14157 Huddinge/Stockholm, Sweden.
Elin Holter Anthonisen
Nina Gustafsson
Nicolas Venteclef
Kirsten Robertson Remen
Anastasios E Damdimopoulos
Anastasia Galeeva
Markku Pelto-Huikko
Enzo Lalli
Knut R Steffensen
Jan-Ake Gustafsson
Eckardt Treuter
Karolinska Institutet · SECentre National de la Recherche Scientifique · FRTampere University · FITampere University · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic and experimental evidence points to a critical involvement of the atypical mammalian orphan receptor DAX-1 in reproductive development and steroidogenesis. Unlike conventional nuclear receptors, DAX-1 appears not to function as a DNA-bound transcription factor. Instead, it has acquired the capability to act as a transcriptional corepressor of steroidogenic factor 1 (SF-1). The interplay of DAX-1 and SF-1 is considered a central, presumably ligand-independent element of adrenogonadal development and function that requires tight regulation. This raises a substantial interest in identifying its modulators and the regulatory signals involved. Here, we uncover molecular mechanisms that link DAX-1 to the ubiquitin modification system via functional interaction with the E3 ubiquitin ligase RNF31. We demonstrate that RNF31 is coexpressed with DAX-1 in steroidogenic tissues and participates in repressing steroidogenic gene expression. We provide evidence for the in vivo existence of a corepressor complex containing RNF31 and DAX-1 at the promoters of the StAR and CYP19 genes. Our data suggest that RNF31 functions to stabilize DAX-1, which might be linked to DAX-1 monoubiquitination. In conclusion, RNF31 appears to be required for DAX-1 to repress transcription, provides means to regulate DAX-1 in ligand-independent ways, and emerges as a relevant coregulator of steroidogenic pathways governing physiology and disease.

Indexed as

Transcription, GeneticCell Line, TumorDAX-1 Orphan Nuclear ReceptorDNA-Binding ProteinsDown-RegulationHumansProtein StabilityReceptors, Retinoic AcidRepressor ProteinsSteroidogenic Factor 1SteroidsUbiquitin-Protein LigasesDAX-1 Orphan Nuclear ReceptorDNA-Binding ProteinsNR0B1 protein, humanReceptors, Retinoic AcidRepressor ProteinsSteroidogenic Factor 1SteroidsUbiquitin-Protein Ligases

Identifiers

PMID19237537
PMCPMC2663311
OpenAlexW2105094132

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.