Evidence map›Paper›PMID 26510866›Full record

ArticleBiology of reproduction2015

GATA4 and GATA6 Knockdown During Luteinization Inhibits Progesterone Production and Gonadotropin Responsiveness in the Corpus Luteum of Female Mice.

Scott M Convissar, Jill Bennett, Sarah C Baumgarten, John P Lydon, Francesco J DeMayo, Carlos Stocco

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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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 2 institutions in 1 country.

Scott M ConvissarDepartment of Physiology and Biophysics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Jill BennettDepartment of Physiology and Biophysics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Sarah C BaumgartenDepartment of Physiology and Biophysics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois.
John P LydonDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Francesco J DeMayoDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Carlos StoccoDepartment of Physiology and Biophysics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois costocco@uic.edu.
University of Illinois Chicago · USBaylor College of Medicine · US

Funding

Environmental Signaling in Reproduction and PregnancyZIAES103311 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI DEMAYO, FRANCESCO · 2016 to 2025
$30.5M
TRAINING IN CELLULAR SIGNALLING IN THE CARDIOVASCULAR SYT32HL007692 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SOLARO, R JOHN · 1990 to 2014
$8.5M
Molecular Analysis of Uterine ReceptivityR01HD042311 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI LYDON, JOHN P · 2009 to 2023
$4.8M
Molecular Pathways Controlling Ovarian Gene ExpressionR01HD057110 · NICHD · YALE UNIVERSITY · PI STOCCO, CARLOS OSCAR · 2009 to 2013
$1.5M
Regulation of Aromatase Expression in the Corpus LuteumR21HD066233 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI STOCCO, CARLOS OSCAR · 2011 to 2012
$393k
NHLBI NIH HHS T32 HL007692NHLBI NIH HHS T32HL07692NICHD NIH HHS R01 HD042311NICHD NIH HHS R01 HD057110NICHD NIH HHS R01HD057110NICHD NIH HHS R21 HD066233NICHD NIH HHS R21HD066233
6 · The paper itself

Abstract

The surge of luteinizing hormone triggers the genomic reprogramming, cell differentiation, and tissue remodeling of the ovulated follicle, leading to the formation of the corpus luteum. During this process, called luteinization, follicular granulosa cells begin expressing a new set of genes that allow the resulting luteal cells to survive in a vastly different hormonal environment and to produce the extremely high amounts of progesterone (P4) needed to sustain pregnancy. To better understand the molecular mechanisms involved in the regulation of luteal P4 production in vivo, the transcription factors GATA4 and GATA6 were knocked down in the corpus luteum by crossing mice carrying Gata4 and Gata6 floxed genes with mice carrying Cre recombinase fused to the progesterone receptor. This receptor is expressed exclusively in granulosa cells after the luteinizing hormone surge, leading to recombination of floxed genes during follicle luteinization. The findings demonstrated that GATA4 and GATA6 are essential for female fertility, whereas targeting either factor alone causes subfertility. When compared to control mice, serum P4 levels and luteal expression of key steroidogenic genes were significantly lower in conditional knockdown mice. The results also showed that GATA4 and GATA6 are required for the expression of the receptors for prolactin and luteinizing hormone, the main luteotropic hormones in mice. The findings demonstrate that GATA4 and GATA6 are crucial regulators of luteal steroidogenesis and are required for the normal response of luteal cells to luteotropins.

Indexed as

AnimalsChorionic GonadotropinCorpus LuteumFemaleGATA4 Transcription FactorGATA6 Transcription FactorGene Knockdown TechniquesGranulosa CellsInfertility, FemaleLuteinizationMiceProgesteroneReceptors, ProgesteroneChorionic GonadotropinGata4 protein, mouseGATA4 Transcription FactorGata6 protein, mouseGATA6 Transcription FactorProgesteroneReceptors, Progesteronecorpus luteumfemale infertilityGATAluteinizing hormone (LH/LH receptor)progesterone/progesterone receptor

Identifiers

PMID26510866
PMCPMC4712692
OpenAlexW1821524341

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.