Evidence map›Paper›PMID 23275456›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2013

GnRH increases c-Fos half-life contributing to higher FSHβ induction.

Gaddameedi R Reddy, Changchuan Xie, Lacey L Lindaman, Djurdjica Coss

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  3. Obesity Alters POMC and Kisspeptin Neuron Cross Talk Leading to Reduced Luteinizing Hormone in Male Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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  4. Article
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  6. Review
  7. Article
  8. PACAP induces FSHβ gene expression via EPAC.Molecular and cellular endocrinology · 2019
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Previous Ketamine Produces an Enduring Blockade of Neurochemical and Behavioral Effects of Uncontrollable Stress.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

4 authors at 1 institution in 1 country.

Gaddameedi R ReddyDepartment of Reproductive Medicine, University of California San Diego, La Jolla, California 92093-0674, USA.
Changchuan Xie
Lacey L Lindaman
Djurdjica Coss
University of California, San Diego · US

Funding

The Interaction of Neuroendocrine Repro. Function and Metabolic SignalingU54HD012303 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MELLON, PAMELA L · 1999 to 2013
$18.0M
The Role of FSH in Female InfertilityP50HD012303 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LAWSON, MARK ANDREW · 1985 to 2020
$7.5M
The Role of AP-1 in the GonadotropeR01HD057549 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI COSS, DJURDJICA · 2009 to 2013
$1.6M
GnRH-Regulated Transcriptome in the GonadotropeR21HD058752 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI COSS, DJURDJICA · 2009 to 2010
$425k
NICHD NIH HHS P50 HD012303NICHD NIH HHS R01 HD057549NICHD NIH HHS R21 HD058752NICHD NIH HHS U54 HD012303NICHD NIH HHS U54 HD12303
6 · The paper itself

Abstract

GnRH is a potent hypothalamic regulator of gonadotropin hormones, LH and FSH, which are both expressed within the pituitary gonadotrope and are necessary for the stimulation of gametogenesis and steroidogenesis in the gonads. Differential regulation of LH and FSH, which is essential for reproductive fitness, is achieved, in part, through the varying of GnRH pulse frequency. However, the mechanism controlling the increase in FSH during the periods of low GnRH has not been elucidated. Here, we uncover another level of regulation by GnRH that contributes to differential expression of the gonadotropins and may play an important role for the generation of the secondary rise of FSH that stimulates folliculogenesis. GnRH stimulates LHβ and FSHβ subunit transcription via induction of the immediate early genes, Egr1 and c-Fos, respectively. Here, we determined that GnRH induces rapidly both Egr1 and c-Fos, but specifically decreases the rate of c-Fos degradation. In particular, GnRH modulates the rate of c-Fos protein turnover by inducing c-Fos phosphorylation through the ERK1/2 pathway. This extends the half-life of c-Fos, which is normally rapidly degraded. Confirming the role of phosphorylation in promoting increased protein activity, we show that a c-Fos mutant that cannot be phosphorylated by GnRH induces lower expression of the FHSβ promoter than wild-type c-Fos. Our studies expand upon the role of GnRH in the regulation of gonadotropin gene expression by highlighting the role of c-Fos posttranslational modification that may cause higher levels of FSH during the time of low GnRH pulse frequency to stimulate follicular growth.

Indexed as

AnimalsCell LineEarly Growth Response Protein 1Extracellular Signal-Regulated MAP KinasesFemaleFollicle Stimulating Hormone, beta SubunitGene ExpressionGene Expression RegulationGonadotropin-Releasing HormoneGonadotropinsLuteinizing Hormone, beta SubunitMiceMutationOvarian FolliclePhosphorylationPituitary GlandEarly Growth Response Protein 1Egr1 protein, mouseExtracellular Signal-Regulated MAP KinasesFollicle Stimulating Hormone, beta SubunitGonadotropin-Releasing HormoneGonadotropinsLuteinizing Hormone, beta SubunitProto-Oncogene Proteins c-fos

Identifiers

PMID23275456
PMCPMC3683808
OpenAlexW2073313862

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.