Evidence map›Paper›PMID 24932804›Full record

ArticleEndocrinology2014

Histone deacetylase inhibition induces long-lasting changes in maternal behavior and gene expression in female mice.

Danielle S Stolzenberg, Jacqueline S Stevens, Emilie F Rissman

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 43 citations in OpenAlex.

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  9. Signatures of sex: Sex differences in gene expression in the vertebrate brain.Wiley interdisciplinary reviews. Developmental biology · 2020
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  17. Dynamic modulation of sociality and aggression: an examination of plasticity within endocrine and neuroendocrine systems.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    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 2 institutions in 1 country.

Danielle S StolzenbergDepartment of Psychology (D.S.S.), University of California, Davis, Davis, California 95616; and Department of Biochemistry and Molecular Genetics (J.S.S., E.F.R.), University of Virginia School of Medicine, Charlottesville, Virginia 22908.
Jacqueline S Stevens
Emilie F Rissman
University of Virginia · USUniversity of California, Davis · US

Funding

Research Training in Neuroendocrinology and MetabolismT32DK007646 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ZHENQI LIU · 1990 to 2026
$4.9M
GENETIC AND NEUROENDOCRINE CONTROL OF BEHAVIORAL SYSTEMSR01MH057759 · NIMH · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI RISSMAN, EMILIE F. · 1999 to 2013
$4.0M
NIDDK NIH HHS T32 DK007646NIMH NIH HHS R01 MH057759
6 · The paper itself

Abstract

In many species, including mice, maternal responsiveness is experience-dependent and permanent, lasting for long periods (months to years). We have shown that after brief exposures to pups, virgin female mice continue to respond maternally toward pups for at least one month. Administration of a histone deacetylase inhibitor (HDACi) reduces the amount of maternal experience required to affect maternal behavior and gene expression. In this set of studies, we examined the epigenetic mechanisms that underlie these motivated behaviors. We assessed whether the effects of HDACi persisted 1 month after the initial experience (in the absence of continued pup experience or HDACi treatment) and whether the maintenance of maternal memory was associated with stable changes in gene expression. Using chromatin immunoprecipitation, we examined whether Esr2 and Oxt gene expression might be mediated by recruitment of the histone acetyltransferase cAMP response element binding protein (CBP) to their promoter regions after maternal memory consolidation. We report that HDACi treatment induced long-lasting changes in maternal responsiveness. Maternal learning was associated with increased recruitment of CBP to the Esr2 and Oxt gene promoters during the consolidation of maternal memory as well as a persistent increase in estrogen receptor-β (Esr2) mRNA and decreased expression of the de novo DNA methyltransferase Dnmt3a within the medial preoptic area. The consolidation of the maternal experience may involve the CBP recruitment and stable changes in gene expression, which maintain increased maternal responsiveness for long periods of time.

Indexed as

AnimalsCyclic AMP Response Element-Binding ProteinEstrogen Receptor betaFemaleGene ExpressionHistone Deacetylase InhibitorsHistone DeacetylasesHumansMaleMaternal BehaviorMiceMice, Inbred C57BLMother-Child RelationsPromoter Regions, GeneticCyclic AMP Response Element-Binding ProteinEstrogen Receptor betaHistone Deacetylase InhibitorsHistone Deacetylases

Identifiers

PMID24932804
PMCPMC4138561
OpenAlexW2063080783

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.