Evidence map›Paper›PMID 18550775›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2008

A composite element that binds basic helix loop helix and basic leucine zipper transcription factors is important for gonadotropin-releasing hormone regulation of the follicle-stimulating hormone beta gene.

Nick A Ciccone, Charlemagne T Lacza, Melody Y Hou, Susan J Gregory, Kyung-Yoon Kam, Shuyun Xu, Ursula B Kaiser

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. GnRH pulse frequency is decoded by distinct GαHormones (Athens, Greece) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. GnRH-A Key Regulator of FSH.Endocrinology · 2019
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  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

7 authors at 2 institutions in 1 country.

Nick A CicconeBrigham and Women's Hospital, Division of Endocrinology, Diabetes and Hypertension, 221 Longwood Avenue, Boston, Massachusetts 0211, USA.
Charlemagne T Lacza
Melody Y Hou
Susan J Gregory
Kyung-Yoon Kam
Shuyun Xu
Ursula B Kaiser
Harvard University · USBrigham and Women's Hospital · US

Funding

Reproductive physiology of gonadotropin synthesisR37HD019938 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI Ursula B. Kaiser · 2019 to 2026
$4.3M
REPRODUCTIVE PHYSIOLOGY OF LUTROPIN SYNTHESISR01HD019938 · NICHD · JOSLIN DIABETES CENTER · PI KAISER, URSULA B. · 1985 to 2017
$3.9M
Reproductive Biology of Gonadotropin RegulationR01HD033001 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI KAISER, URSULA B · 2001 to 2005
$1.5M
NICHD NIH HHS HD19938NICHD NIH HHS R01 HD019938NICHD NIH HHS R01 HD033001NICHD NIH HHS R01 HD33001NICHD NIH HHS R37 HD019938
6 · The paper itself

Abstract

Although FSH plays an essential role in controlling gametogenesis, the biology of FSHbeta transcription remains poorly understood, but is known to involve the complex interplay of multiple endocrine factors including GnRH. We have identified a GnRH-responsive element within the rat FSHbeta promoter containing an E-box and partial cAMP response element site that are bound by the basic helix loop helix transcription factor family members, upstream stimulating factor (USF)-1/USF-2, and the basic leucine zipper member, cAMP response element-binding protein (CREB), respectively. Expression studies with CREB, USF-1/USF-2, and activating protein-1 demonstrated that the USF transcription factors increased basal transcription, an effect not observed if the cognate binding site was mutated. Conversely, expression of a dominant negative CREB mutant or CREB knockdown attenuated induction by GnRH, whereas dominant negative Fos or USF had no effect on the GnRH response. GnRH stimulation specifically induced an increase in phosphorylated CREB occupation of the FSHbeta promoter, leading to the recruitment of CREB-binding protein to enhance gene transcription. In conclusion, a composite element bound by both USF and CREB serves to integrate signals for basal and GnRH-stimulated transcription of the rat FSHbeta gene.

Indexed as

Gene Expression RegulationAnimalsBase SequenceBasic Helix-Loop-Helix ProteinsBasic-Leucine Zipper Transcription FactorsBinding SitesCell LineCREB-Binding ProteinCyclic AMP Response Element-Binding ProteinDNA Mutational AnalysisFollicle Stimulating Hormone, beta SubunitGenes, DominantGonadotropin-Releasing HormoneHistone AcetyltransferasesMiceMolecular Sequence DataBasic Helix-Loop-Helix ProteinsBasic-Leucine Zipper Transcription FactorsCREB-Binding ProteinCyclic AMP Response Element-Binding ProteinFollicle Stimulating Hormone, beta SubunitGonadotropin-Releasing HormoneHistone AcetyltransferasesProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-junUpstream Stimulatory Factors

Identifiers

PMID18550775
PMCPMC2725769
OpenAlexW2160066987

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.