Evidence map›Paper›PMID 24379407›Full record

ArticleThe Journal of biological chemistry2014

Control of Foxo1 gene expression by co-activator P300.

Anne R Wondisford, Lishou Xiong, Evan Chang, Shumei Meng, David J Meyers, Mingsong Li, Philip A Cole, Ling He

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.9field-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

37 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. FOXO inBiology · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Regulation of energy metabolism in human pluripotent stem cells.Cellular and molecular life sciences : CMLS · 2021
    Review
  13. Exploring the Genetic Conception of Obesity via the Dual Role of FoxO.International journal of molecular sciences · 2021
    Review
  14. Review
  15. Identification ofFrontiers in pharmacology · 2021
    Article
  16. Nutrients · 2020
    Article
  17. Article
  18. Article
  19. Review
  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

8 authors at 3 institutions in 2 countries.

Anne R WondisfordFrom the Division of Metabolism, Department of Pediatrics and.
Lishou Xiong
Evan Chang
Shumei Meng
David J Meyers
Mingsong Li
Philip A Cole
Ling He
Johns Hopkins University · USJohns Hopkins Medicine · USSouthern Medical University · CN

Funding

JHU-UMD Diabetes Research CenterP30DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI AHIMA, REXFORD S. · 2013 to 2017
$9.7M
Diabetes Research and Training CenterP60DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI WONDISFORD, FREDRIC E. · 2008 to 2012
$9.1M
Transcriptional coactivators and hepatic glucose productionR01DK063349 · NIDDK · UNIVERSITY OF CHICAGO · PI WONDISFORD, FREDRIC E. · 2002 to 2017
$5.0M
Protein Acylation and Methylation Mechanisms_Administrative SupplementR37GM062437 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COLE, PHILIP A · 2013 to 2022
$4.1M
The Distinct Role of CBP and p300 in Regulating Hepatic Glucose ProductionR00DK085142 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI HE, LING · 2011 to 2013
$726k
NIDDK NIH HHS P30 DK079637NIDDK NIH HHS P60 DK079637NIDDK NIH HHS P60DK079637NIDDK NIH HHS R00 DK085142NIDDK NIH HHS R00DK085142NIDDK NIH HHS R01 DK063349NIGMS NIH HHS R37 GM062437NIGMS NIH HHS R37GM62437
6 · The paper itself

Abstract

FOXO1 is an important downstream mediator of the insulin signaling pathway. In the fed state, elevated insulin phosphorylates FOXO1 via AKT, leading to its nuclear exclusion and degradation. A reduction in nuclear FOXO1 levels then leads to suppression of hepatic glucose production. However, the mechanism leading to expression of Foxo1 gene in the fasted state is less clear. We found that Foxo1 mRNA and FOXO1 protein levels of Foxo1 were increased significantly in the liver of mice after 16 h of fasting. Furthermore, dibutyrl cAMP stimulated the expression of Foxo1 at both mRNA and protein level in hepatocytes. Because cAMP-PKA regulates hepatic glucose production through cAMP-response element-binding protein co-activators, we depleted these co-activators using adenoviral shRNAs. Interestingly, only depletion of co-activator P300 resulted in the decrease of Foxo1 mRNA and FOXO1 protein levels. In addition, inhibition of histone acetyltransferase activity of P300 significantly decreased hepatic Foxo1 mRNA and FOXO1 protein levels in fasted mice, as well as fasting blood glucose levels. By characterization of Foxo1 gene promoter, P300 regulates the Foxo1 gene expression through the binding to tandem cAMP-response element sites in the proximal promoter region of Foxo1 gene.

Indexed as

AnimalsBucladesineCell Line, TumorCyclic AMP Response Element-Binding ProteinFastingForkhead Box Protein O1Forkhead Transcription FactorsGene Expression RegulationLiverMiceBucladesineCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinForkhead Box Protein O1Forkhead Transcription FactorsFoxo1 protein, mouseCREBFoxoGluconeogenesisHistone AcetylaseP300

Identifiers

PMID24379407
PMCPMC3924295
OpenAlexW2048341249

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.