Evidence map›Paper›PMID 20080871›Full record

ArticleEndocrinology2010

Involvement of transducer of regulated cAMP response element-binding protein activity on corticotropin releasing hormone transcription.

Ying Liu, Ana G Coello, Valery Grinevich, Greti Aguilera

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Central Administration of Cyclosporine A Decreases Ethanol Drinking.Alcohol and alcoholism (Oxford, Oxfordshire) · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Novel aspects of glucocorticoid actions.Journal of neuroendocrinology · 2014
    Review
  13. Article
  14. Article
  15. Transcriptional regulation of episodic glucocorticoid secretion.Molecular and cellular endocrinology · 2013
    Review
  16. Review
  17. The molecular physiology of CRH neurons.Frontiers in neuroendocrinology · 2012
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Ying LiuSection on Endocrine Physiology, Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, 10 Center Drive, Bethesda, Maryland 20892, USA.
Ana G Coello
Valery Grinevich
Greti Aguilera
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USMax Planck Institute for Medical Research · DENational Institutes of Health · US

Funding

Neuroendocrine Control Of The Stress ResponseZIAHD000631 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI AGUILERA, GRETI · 2009 to 2014
$4.0M
Intramural NIH HHS
6 · The paper itself

Abstract

We have recently shown that phospho-cAMP response element-binding protein (CREB) is essential but not sufficient for activation of CRH transcription, suggesting the requirement of a coactivator. Here, we test the hypothesis that the CREB coactivator, transducer of regulated CREB activity (TORC), is required for activation of CRH transcription, using the cell line 4B and primary cultures of hypothalamic neurons. Immunohistochemistry and Western blot experiments in 4B cells revealed time-dependent nuclear translocation of TORC1,TORC 2, and TORC3 by forskolin [but not by the phorbol ester, phorbol 12-myristate 13-acetate (PMA)] in a concentration-dependent manner. In reporter gene assays, cotransfection of TORC1 or TORC2 potentiated the stimulatory effect of forskolin on CRH promoter activity but had no effect in cells treated with PMA. Knockout of endogenous TORC using silencing RNA markedly inhibited forskolin-activated CRH promoter activity in 4B cells, as well as the induction of endogenous CRH primary transcript by forskolin in primary neuronal cultures. Coimmunoprecipitation and chromatin immunoprecipitation experiments in 4B cells revealed association of CREB and TORC in the nucleus, and recruitment of TORC2 by the CRH promoter, after 20-min incubation with forskolin. These studies demonstrate a correlation between nuclear translocation of TORC with association to the CRH promoter and activation of CRH transcription. The data suggest that TORC is required for transcriptional activation of the CRH promoter by acting as a CREB coactivator. In addition, cytoplasmic retention of TORC during PMA treatment is likely to explain the failure of phorbolesters to activate CRH transcription in spite of efficiently phosphorylating CREB.

Indexed as

AnimalsCell LineCell NucleusColforsinCorticotropin-Releasing HormoneCyclic AMP Response Element-Binding ProteinGenes, ReporterHypothalamusPromoter Regions, GeneticRatsRNA, Small InterferingTetradecanoylphorbol AcetateTrans-ActivatorsTranscriptional ActivationTranscription FactorsColforsinCorticotropin-Releasing HormoneCreb1 protein, ratCrtc1 protein, ratCRTC2 protein, ratCyclic AMP Response Element-Binding ProteinRNA, Small InterferingTetradecanoylphorbol AcetateTrans-ActivatorsTranscription Factors

Identifiers

PMID20080871
PMCPMC2840689
OpenAlexW2082938876

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.