Evidence map›Paper›PMID 30127461›Full record

ArticleNature communications2018

Epigenetic regulation of the circadian gene Per1 contributes to age-related changes in hippocampal memory.

Janine L Kwapis, Yasaman Alaghband, Enikö A Kramár, Alberto J López, Annie Vogel Ciernia, André O White, Guanhua Shu, Diane Rhee, Christina M Michael, Emilie Montellier and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

111 citing papers in PubMed, 166 citations in OpenAlex.

  1. Article
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  4. Advances and clinical potential of epigenome editing.Cellular and molecular life sciences : CMLS · 2026
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  10. Epigenome editing based treatment: Progresses and challenges.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Review
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  19. Review
  20. Article

51 more citing papers are in PubMed but not listed here.

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

17 authors at 3 institutions in 1 country.

Janine L KwapisDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Yasaman AlaghbandDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Enikö A KramárDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Alberto J LópezDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Annie Vogel CierniaDepartment of Medical Microbiology and Immunology, University of California, Davis, CA, 95616, USA.
André O WhiteDepartment of Biological Sciences, Mount Holyoke College, South Hadley, MA, 01075, USA.
Guanhua ShuDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Diane RheeDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Christina M MichaelDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Emilie MontellierCenter for Epigenetics and Metabolism, Department of Biological Chemistry, University of California, Irvine, CA, 92697, USA.
Yu LiuDepartment of Computer Science, University of California, Irvine, CA, 92697, USA.
Christophe N MagnanDepartment of Computer Science, University of California, Irvine, CA, 92697, USA.
Siwei ChenDepartment of Computer Science, University of California, Irvine, CA, 92697, USA.
Paolo Sassone-CorsiCenter for Epigenetics and Metabolism, Department of Biological Chemistry, University of California, Irvine, CA, 92697, USA.
Pierre BaldiDepartment of Computer Science, University of California, Irvine, CA, 92697, USA.
Dina P MatheosDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Marcelo A WoodDepartment of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA. mwood@uci.edu.
University of California, Irvine · USMount Holyoke College · USUniversity of California Davis Medical Center · US

Funding

Training in the Neurobiology of Aging and Alzheimers DiseaseT32AG000096 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI VIVEK SWARUP, Craig E Stark · 1985 to 2026
$9.6M
Exercise-induced epigenetic mechanisms underlying neuronal plasticity and cognitionR01AG051807 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI COTMAN, CARL WAYNE, WOOD, MARCELO ANDRES · 2016 to 2020
$3.1M
Bioinformatics Tools for Circadian BiologyR01GM123558 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Pierre Baldi · 2017 to 2026
$2.4M
Role of Neuron-Specific Nucleosome Remodeling in Intellectual DisabilityR01MH101491 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI LYNCH, GARY S, WOOD, MARCELO ANDRES · 2013 to 2017
$2.3M
Role of HDAC3 in repressing memory formation in the aging brainR21AG050787 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI WOOD, MARCELO ANDRES · 2016 to 2017
$425k
Epigenetic regulation of the circadian gene Per1 in age-related memory impairmentsK99AG056596 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI KWAPIS, JANINE LYNN · 2017 to 2018
$201k
Epigenetic repression of synaptic plasticity and memory in the aging brainF32AG052303 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI KWAPIS, JANINE LYNN · 2015 to 2017
$88k
NIA NIH HHS F32 AG052303NIA NIH HHS K99 AG056596NIA NIH HHS R01 AG051807NIA NIH HHS R21 AG050787NIA NIH HHS T32 AG000096NIGMS NIH HHS R01 GM123558NIMH NIH HHS R01 MH101491
6 · The paper itself

Abstract

Aging is accompanied by impairments in both circadian rhythmicity and long-term memory. Although it is clear that memory performance is affected by circadian cycling, it is unknown whether age-related disruption of the circadian clock causes impaired hippocampal memory. Here, we show that the repressive histone deacetylase HDAC3 restricts long-term memory, synaptic plasticity, and experience-induced expression of the circadian gene Per1 in the aging hippocampus without affecting rhythmic circadian activity patterns. We also demonstrate that hippocampal Per1 is critical for long-term memory formation. Together, our data challenge the traditional idea that alterations in the core circadian clock drive circadian-related changes in memory formation and instead argue for a more autonomous role for circadian clock gene function in hippocampal cells to gate the likelihood of long-term memory formation.

Indexed as

Epigenesis, GeneticAgingAnimalsCircadian RhythmGene DeletionGene Knockdown TechniquesHippocampusHistone Deacetylase 3Histone DeacetylasesLong-Term PotentiationMemoryMemory DisordersMice, Inbred C57BLNeuronal PlasticityPeriod Circadian ProteinsHistone Deacetylase 3Histone DeacetylasesPer1 protein, mousePeriod Circadian Proteins

Identifiers

PMID30127461
PMCPMC6102273
OpenAlexW2886406130

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.