Evidence map›Paper›PMID 24064357›Full record

ArticleEndocrinology2013

GATA4 and GATA6 silencing in ovarian granulosa cells affects levels of mRNAs involved in steroidogenesis, extracellular structure organization, IGF-I activity, and apoptosis.

Jill Bennett, Sarah C Baumgarten, Carlos Stocco

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  5. Identification of FSH-regulated and estrous stage-specific transcriptional networks in mouse ovaries.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  15. ERβ Regulation of Gonadotropin Responses during Folliculogenesis.International journal of molecular sciences · 2021
    Review
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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

3 authors at 1 institution in 1 country.

Jill BennettDepartment of Physiology and Biophysics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois 606012. costocco@uic.edu.
Sarah C Baumgarten
Carlos Stocco
University of Illinois Chicago · US

Funding

TRAINING IN CELLULAR SIGNALLING IN THE CARDIOVASCULAR SYT32HL007692 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SOLARO, R JOHN · 1990 to 2014
$8.5M
REPRODUCTIVE BIOLOGY--MULTIDISCIPLINARYT32HD007133 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI ROSELLI, CHARLES E. · 1985 to 2014
$2.2M
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 HL007692NICHD NIH HHS R01 HD057110NICHD NIH HHS R01HD057110NICHD NIH HHS R21 HD066233NICHD NIH HHS R21HD066233NICHD NIH HHS T32 HD007133
6 · The paper itself

Abstract

Knockdown of the transcription factors GATA4 and GATA6 in granulosa cells (GCs) impairs folliculogenesis and induces infertility. To investigate the pathways and genes regulated by these factors, we performed microarray analyses on wild-type GCs or GCs lacking GATA4, GATA6, or GATA4/6 (G4(gcko), G6(gcko), and G4/6(gcko)) after in vivo treatment with equine chorionic gonadotropin. GATA4 deletion affected a greater number of genes than GATA6, which correlates with the subfertility observed in G4(gcko) mice and the normal reproductive function found in G6(gcko) animals. An even greater number of genes were affected by the deletion of both factors. Moreover, the expression of FSH receptor, LH receptor, inhibin α and β, versican, pregnancy-associated plasma protein A, and the regulatory unit 2b of protein kinase A, which are known to be crucial for ovarian function, was greatly affected in double GATA4 and GATA6 knockouts when compared with single GATA-deficient animals. This suggests that GATA4 and GATA6 functionally compensate for each other in the regulation of key ovarian genes. Functional enrichment revealed that ovulation, growth, intracellular signaling, extracellular structure organization, gonadotropin and growth factor actions, and steroidogenesis were significantly regulated in G4/6(gcko) mice. The results of this analysis were confirmed using quantitative polymerase chain reaction, immunohistochemical, and biological assays. Treatment of GCs with cAMP/IGF-I, to bypass FSH and IGF-I signaling defects, revealed that most of the affected genes are direct targets of GATA4/6. The diversity of pathways affected by the knockdown of GATA underscores the important role of these factors in the regulation of GC function.

Indexed as

Gene SilencingAnimalsApoptosisFemaleFollicle Stimulating HormoneGATA4 Transcription FactorGATA6 Transcription FactorGranulosa CellsInsulin-Like Growth Factor Binding ProteinsInsulin-Like Growth Factor IMiceMice, KnockoutPregnancyRNA, MessengerSignal TransductionSteroidsFollicle Stimulating HormoneGata4 protein, mouseGATA4 Transcription FactorGata6 protein, mouseGATA6 Transcription FactorInsulin-Like Growth Factor Binding ProteinsInsulin-Like Growth Factor IRNA, MessengerSteroids

Identifiers

PMID24064357
PMCPMC3836082
OpenAlexW1968119300

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.