Evidence map›Paper›PMID 18184656›Full record

ArticleThe Journal of biological chemistry2008

Phosphorylation of CtBP1 by cAMP-dependent protein kinase modulates induction of CYP17 by stimulating partnering of CtBP1 and 2.

Eric B Dammer, Marion B Sewer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. MicroRNA in Ovarian Biology and Disease.Cold Spring Harbor perspectives in medicine · 2015
    Review
  5. Article
  6. Components of the CtBP1/BARS-dependent fission machinery.Histochemistry and cell biology · 2013
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Role of Dicer in female fertility.Trends in endocrinology and metabolism: TEM · 2009
    Review
  15. Review
  16. Complex assembly on the human CYP17 promoter.Molecular and cellular endocrinology · 2009
    Review
  17. Article
  18. 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

2 authors at 1 institution in 1 country.

Eric B DammerSchool of Biology and Parker H Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia 30332-0230, USA.
Marion B Sewer
Georgia Institute of Technology · US

Funding

Regulation of Steroidogenic Genes by Trophic HormonesR01GM073241 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEWER, MARION B. · 2004 to 2013
$2.2M
Regulation of Steroidogenic Genes by Trophic HormonesR56GM073241 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEWER, MARION B. · 2009 to 2009
$281k
NIGMS NIH HHS GM073241NIGMS NIH HHS R01 GM073241NIGMS NIH HHS R56 GM073241
6 · The paper itself

Abstract

In the human adrenal cortex, the peptide hormone adrenocorticotropin (ACTH) directs cortisol and adrenal androgen biosynthesis by activating a cAMP/cAMP-dependent protein kinase (PKA) pathway. Carboxyl-terminal binding protein 1 (CtBP1) is a corepressor that regulates transcription of the CYP17 gene by periodically interacting with steroidogenic factor-1 in response to ACTH signaling. Given that CtBP1 function is regulated by NADH binding, we hypothesized that ACTH-stimulated changes in cellular pyridine nucleotide concentrations modulate the ability of CtBP1 to repress CYP17 transcription. Further, we postulated that PKA evokes changes in the phosphorylation status of CtBP1 that control the ability of the protein to bind to steroidogenic factor-1 and the coactivator GCN5 (general control nonderepressed 5) and repress CYP17 gene expression. We show that ACTH alters pyridine nucleotide redox state and identify amino acid residues in CtBP1 that are targeted by PKA and PAK6. Both ACTH/cAMP signaling and NADH/NAD+ ratio stimulate nuclear-cytoplasmic oscillation of both CtBP proteins. We provide evidence that PKA 1) induces metabolic changes in the adrenal cortex and 2) phosphorylates CtBP proteins, particularly CtBP1 at T144, resulting in CtBP protein partnering and ACTH-dependent CYP17 transcription.

Indexed as

Gene Expression Regulation, NeoplasticAdrenocorticotropic HormoneAlcohol OxidoreductasesCell Line, TumorCell NucleusCo-Repressor ProteinsCyclic AMPCytoplasmDNA-Binding ProteinsEye ProteinsHumansModels, BiologicalNerve Tissue ProteinsNucleotidesPhosphorylationPyridinesAdrenocorticotropic HormoneAlcohol OxidoreductasesCo-Repressor ProteinsCTBP2 protein, humanC-terminal binding proteinCyclic AMPDNA-Binding ProteinsEye ProteinsNerve Tissue ProteinsNucleotidespyridinePyridinesSteroid 17-alpha-Hydroxylase

Identifiers

PMID18184656
PMCPMC2730192
OpenAlexW1973952654

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.