Evidence map›Paper›PMID 19406940›Full record

ArticleEndocrinology2009

Computational and functional analysis of growth hormone (GH)-regulated genes identifies the transcriptional repressor B-cell lymphoma 6 (Bc16) as a participant in GH-regulated transcription.

Yili Chen, Grace Lin, Jeffrey S Huo, Deborah Barney, Zhenni Wang, Tamara Livshiz, David J States, Zhaohui S Qin, Jessica Schwartz

Open access · greenAbstract read
In one paragraph

Article in Endocrinology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. The Role of PIK3R1 in Metabolic Function and Insulin Sensitivity.International journal of molecular sciences · 2023
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. BCL6 controls Th9 cell development by repressing Il9 transcription.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Article
  13. Minireview: mechanisms of growth hormone-mediated gene regulation.Molecular endocrinology (Baltimore, Md.) · 2014
    Review
  14. Article
  15. Article
  16. Mapping the growth hormone--Stat5b--IGF-I transcriptional circuit.Trends in endocrinology and metabolism: TEM · 2012
    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

9 authors at 1 institution in 1 country.

Yili ChenDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48109-5622. jeschwar@umich.edu.
Grace Lin
Jeffrey S Huo
Deborah Barney
Zhenni Wang
Tamara Livshiz
David J States
Zhaohui S Qin
Jessica Schwartz
University of Michigan–Ann Arbor · US

Funding

Nation Center- Integrative Biomedical Informatics(RMI)U54DA021519 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATHEY, BRIAN DAVID · 2005 to 2010
$21.3M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
GROWTH HORMONE SIGNALING TO THE NUCLEUSR01DK046072 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHWARTZ, JESSICA · 1996 to 2010
$2.3M
Representing and Acquiring Knowledge of Genome RegulatioR01LM008106 · NLM · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STATES, DAVID J · 2003 to 2006
$1.3M
C/EBPb and heterochromatin: their role in adipogenesisR03TW008143 · FIC · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHWARTZ, JESSICA · 2009 to 2011
$103k
FIC NIH HHS R03 TW008143NIDA NIH HHS U54 DA021519NIDDK NIH HHS DK46072NIDDK NIH HHS R01 DK046072NIGMS NIH HHS T32 GM007315NIGMS NIH HHS T32 GM07315NLM NIH HHS R01 LM008106
6 · The paper itself

Abstract

For insight into transcriptional mechanisms mediating physiological responses to GH, data mining was performed on a profile of GH-regulated genes induced or inhibited at different times in highly responsive 3T3-F442A adipocytes. Gene set enrichment analysis indicated that GH-regulated genes are enriched in pathways including phosphoinositide and insulin signaling and suggested that suppressor of cytokine signaling 2 (SOCS2) and phosphoinositide 3' kinase regulatory subunit p85alpha (Pik3r1) are important targets. Model-based Chinese restaurant clustering identified a group of genes highly regulated by GH at times consistent with its key physiological actions. This cluster included IGF-I, phosphoinositide 3' kinase p85alpha, SOCS2, and cytokine-inducible SH2-containing protein. It also contains the most strongly repressed gene in the profile, B cell lymphoma 6 (Bcl6), a transcriptional repressor. Quantitative real-time PCR verified the strong decrease in Bcl6 mRNA after GH treatment and induction of the other genes in the cluster. Transcriptional network analysis of the genes implicated signal transducer and activator of transcription (Stat) 5 as hub regulating the most responsive genes, Igf1, Socs2, Cish, and Bcl6. Transcriptional activation analysis demonstrated that Bcl6 inhibits SOCS2-luciferase and blunts its stimulation by GH. Occupancy of endogenous Bcl6 on SOCS2 DNA decreased after GH treatment, whereas occupancy of Stat5 increased concomitantly. Thus, GH-mediated inhibition of Bcl6 expression may reverse the repression of SOCS2 and facilitate SOCS2 activation by GH. Together these analyses identify Bcl6 as a participant in GH-regulated gene expression and suggest an interplay between the repressor Bcl6 and the activator Stat5 in regulating genes, which contribute to GH responses.

Indexed as

AdipocytesAnimalsCell LineChromatin ImmunoprecipitationComputational BiologyDNA-Binding ProteinsGene Expression RegulationGrowth HormoneImmunoblottingMiceProto-Oncogene Proteins c-bcl-6STAT5 Transcription FactorSuppressor of Cytokine Signaling ProteinsTranscription, GeneticBcl6 protein, mouseDNA-Binding ProteinsGrowth HormoneProto-Oncogene Proteins c-bcl-6Socs2 protein, mouseSTAT5 Transcription FactorSuppressor of Cytokine Signaling Proteins

Identifiers

PMID19406940
PMCPMC2717871
OpenAlexW2172003419

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.