Evidence map›Paper›PMID 25635942›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2015

Rapid communication: A microRNA-132/212 pathway mediates GnRH activation of FSH expression.

Jérôme Lannes, David L'Hôte, Ghislaine Garrel, Jean-Noël Laverrière, Joëlle Cohen-Tannoudji, Bruno Quérat

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. SIRT1: A Key Player in Male Reproduction.Life (Basel, Switzerland) · 2022
    Review
  7. Article
  8. Article
  9. Epigenetics of functional hypothalamic amenorrhea.Frontiers in endocrinology · 2022
    Review
  10. Review
  11. Post-Transcriptional Regulation ofInternational journal of molecular sciences · 2021
    Review
  12. Sirt1 Activity in the Brain: Simultaneous Effects on Energy Homeostasis and Reproduction.International journal of environmental research and public health · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The Versatility of Sirtuin-1 in Endocrinology and Immunology.Frontiers in cell and developmental biology · 2020
    Review
  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

6 authors at 3 institutions in 1 country.

Jérôme LannesDepartment of Biologie Fonctionnelle et Adaptative, Université Paris-Diderot, Sorbonne Paris Cité, F-75013 Paris, France; Centre National pour la Recherche Scientifique Unité Mixte de Recherche 8251, F-75013 Paris, France; and Institut National de la Santé et de la Recherche Médicale Unité 1133, Physiologie de l'axe Gonadotrope, F-75013 Paris, France.
David L'Hôte
Ghislaine Garrel
Jean-Noël Laverrière
Joëlle Cohen-Tannoudji
Bruno Quérat
Sorbonne Paris Cité · FRPhysiologie De L'Axe GonadotropeInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GnRH plays a key role in the vertebrate reproductive system by stimulating biosynthesis and secretion of pituitary gonadotropins. However, the potential involvement of microRNAs (miRNAs) on this activation has still to be explored. In this study, we investigated the role of miRNA-132 and miRNA-212, two tandemly expressed miRNAs that target the same transcripts, on GnRH-induced FSH expression. We first showed that the GnRH stimulation of FSH secretion was reduced and Fshb mRNA abolished by blocking miR-132/212 action in rat pituitary cells. In mouse LβT2 gonadotrope cells, the GnRH stimulation of Fshb mRNA was also demonstrated to be dependent on miR-132/212 and reproduced by overexpressing one or both miRNAs. We then showed that the miR-132/212-mediated action of GnRH involved a posttranscriptional decrease of sirtuin 1 (SIRT1) deacetylase. The lower level of SIRT1 deacetylase correlated with an increase in the acetylated form of Forkhead Box O1 (FOXO1), a transcriptional repressor of Fshb. Interestingly, we show that the acetylated mimicking mutant of FOXO1 was localized outside the nucleus, thus alleviating its repressive effect on Fshb transcription. Overall, we demonstrate that the GnRH stimulation of Fshb expression is dependent on miR-132/212 and involves a SIRT1-FOXO1 pathway. This is the first demonstration of an obligatory microRNA pathway in the GnRH-regulated expression of a gonadotropin gene.

Indexed as

AcetylationAnimalsFemaleFollicle Stimulating Hormone, beta SubunitForkhead Box Protein O1Forkhead Transcription FactorsGonadotropin-Releasing HormoneHumansMiceMicroRNAsModels, BiologicalRats, WistarSirtuin 1Transcription, GeneticFollicle Stimulating Hormone, beta SubunitForkhead Box Protein O1Forkhead Transcription FactorsFoxo1 protein, mouseGonadotropin-Releasing HormoneMicroRNAsMIRN132 microRNA, mouseMIRN132 microRNA, ratMIRN212 microRNA, mouseMIRN212 microRNA, ratSirtuin 1

Identifiers

PMID25635942
PMCPMC5414753
OpenAlexW2089825221

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.