Evidence map›Paper›PMID 24035865›Full record

ReviewMolecular and cellular endocrinology2014

Translational control of gene expression in the gonadotrope.

Taeshin Kim, Minh-Ha T Do, Mark A Lawson

Abstract readReview
In one paragraph

Review in Molecular and cellular endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Molecular Mechanisms of Pituitary Cell Plasticity.Frontiers in endocrinology · 2020
    Review
  6. Article
  7. Article
  8. Article
  9. Mouse models for the analysis of gonadotropin secretion and action.Best practice & research. Clinical endocrinology & metabolism · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

3 authors at 1 institution in 1 country.

Taeshin KimDepartment of Reproductive Medicine, University of California, San Diego, La Jolla, CA 92093, United States.
Minh-Ha T DoDepartment of Reproductive Medicine, University of California, San Diego, La Jolla, CA 92093, United States.
Mark A LawsonDepartment of Reproductive Medicine, University of California, San Diego, La Jolla, CA 92093, United States. Electronic address: mlawson@ucsd.edu.
University of California, San Diego · US

Funding

Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PETER J TONTONOZ · 2003 to 2026
$40.4M
The Interaction of Neuroendocrine Repro. Function and Metabolic SignalingU54HD012303 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MELLON, PAMELA L · 1999 to 2013
$18.0M
Training Program in Basic Clinical GeneticsT32GM008666 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMILTON, BRUCE A · 1998 to 2021
$8.6M
The Role of FSH in Female InfertilityP50HD012303 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MELLON, PAMELA L · 1985 to 2020
$7.5M
TRAINING IN REPRODUCTIVE SCIENCEST32HD007203 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PAMELA L MELLON · 1988 to 2026
$4.8M
GNRH SIGNALING MECHANISMS IN THE PITUITARY GONADOTROPER01HD037568 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LAWSON, MARK ANDREW · 2000 to 2014
$3.6M
NICHD NIH HHS P50 HD012303NICHD NIH HHS R01 HD 037568NICHD NIH HHS R01 HD037568NICHD NIH HHS T32 HD007203NICHD NIH HHS U54 HD012303NIDDK NIH HHS P30 DK063491NIGMS NIH HHS T32 GM008666NIGMS NIH HHS T32 GM08666
6 · The paper itself

Abstract

The study of gene expression in gonadotropes has largely focused on the variety of mechanisms regulating transcription of the gonadotropin genes and ancillary factors that contribute to the overall phenotype and function of these cells in reproduction. However, there are aspects of the response to GNRH signaling that are not readily explained by changes at the level of transcription. As our understanding of regulation at the level of mRNA translation has increased, it has become evident that GNRH receptor signaling engages multiple aspects of translational regulation. This includes activation of cap-dependent translation initiation, translational pausing caused by the unfolded protein response and RNA binding protein interaction. Gonadotropin mRNAs and the mRNAs of other factors that control the transcriptional and signaling responses to GNRH have been identified as targets of regulation at the level of translation. In this review we examine the impact of translational control of the expression of gonadotropin genes and other genes relevant to GNRH-mediated control of gonadotrope function.

Indexed as

AnimalsGene Expression RegulationGonadotrophsHumansPeptide Chain Initiation, TranslationalReceptors, LHRHSignal TransductionUnfolded Protein ResponseReceptors, LHRHFollicle-stimulating hormoneGonadotropinsLuteinizing hormonePituitaryTranslationUnfolded-protein response

Identifiers

PMID24035865
PMCPMC4009948
OpenAlexW2160349280

What OpenQuestion holds

Textmetadata
LicenceTDM
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.