Evidence map›Paper›PMID 25089620›Full record

ArticlePloS one2014

Nucleolar integrity is required for the maintenance of long-term synaptic plasticity.

Kim D Allen, Andrei V Gourov, Christopher Harte, Peng Gao, Clarice Lee, Darlene Sylvain, Joshua M Splett, William C Oxberry, Paula S van de Nes, Matthew J Troy-Regier and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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
1.2field-weighted citation impact, top 25% 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, 33 citations in OpenAlex.

  1. Regulation of Translation by PKA Signaling Pathway.International journal of molecular sciences · 2026
    Review
  2. Review
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  4. Ribosomal DNA and Neurological Disorders.Current molecular medicine · 2025
    Review
  5. Role of NADCellular and molecular neurobiology · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. 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

13 authors at 3 institutions in 1 country.

Kim D AllenDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America; Department of Biology, School of Science, Health and Technology, City University of New York, Medgar Evers College, Brooklyn, New York, United States of America.
Andrei V GourovDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Christopher HarteDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Peng GaoDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Clarice LeeDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Darlene SylvainDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Joshua M SplettDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
William C OxberryDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America; The Robert F. Furchgott Center for Neural and Behavioral Science, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Paula S van de NesDepartments of Physiology and Pharmacology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Matthew J Troy-RegierDepartments of Physiology and Pharmacology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Jason WolkDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
Juan M AlarconDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America; The Robert F. Furchgott Center for Neural and Behavioral Science, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
A Iván HernándezDepartment of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America; The Robert F. Furchgott Center for Neural and Behavioral Science, State University of New York, Downstate Medical Center, Brooklyn, New York, United States of America.
State University of New York · USSUNY Downstate Health Sciences University · USMedgar Evers College · US

Funding

Decoding place cell firing-induced synaptic plasticity and cognitive mappingR03NS081625 · NINDS · SUNY DOWNSTATE MEDICAL CENTER · PI ALARCON, JUAN MARCOS · 2013 to 2014
$159k
NINDS NIH HHS R03 NS081625
6 · The paper itself

Abstract

Long-term memory (LTM) formation requires new protein synthesis and new gene expression. Based on our work in Aplysia, we hypothesized that the rRNA genes, stimulation-dependent targets of the enzyme Poly(ADP-ribose) polymerase-1 (PARP-1), are primary effectors of the activity-dependent changes in synaptic function that maintain synaptic plasticity and memory. Using electrophysiology, immunohistochemistry, pharmacology and molecular biology techniques, we show here, for the first time, that the maintenance of forskolin-induced late-phase long-term potentiation (L-LTP) in mouse hippocampal slices requires nucleolar integrity and the expression of new rRNAs. The activity-dependent upregulation of rRNA, as well as L-LTP expression, are poly(ADP-ribosyl)ation (PAR) dependent and accompanied by an increase in nuclear PARP-1 and Poly(ADP) ribose molecules (pADPr) after forskolin stimulation. The upregulation of PARP-1 and pADPr is regulated by Protein kinase A (PKA) and extracellular signal-regulated kinase (ERK)--two kinases strongly associated with long-term plasticity and learning and memory. Selective inhibition of RNA Polymerase I (Pol I), responsible for the synthesis of precursor rRNA, results in the segmentation of nucleoli, the exclusion of PARP-1 from functional nucleolar compartments and disrupted L-LTP maintenance. Taken as a whole, these results suggest that new rRNAs (28S, 18S, and 5.8S ribosomal components)--hence, new ribosomes and nucleoli integrity--are required for the maintenance of long-term synaptic plasticity. This provides a mechanistic link between stimulation-dependent gene expression and the new protein synthesis known to be required for memory consolidation.

Indexed as

AnimalsColforsinCyclic AMP-Dependent Protein KinasesGene ExpressionHippocampusLong-Term PotentiationMAP Kinase Signaling SystemMemory, Long-TermMiceNeuronal PlasticityPoly Adenosine Diphosphate RibosePoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesRNA, Ribosomal, 28SSynapsesColforsinCyclic AMP-Dependent Protein KinasesParp1 protein, mousePoly Adenosine Diphosphate RibosePoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesRNA, Ribosomal, 28S

Identifiers

PMID25089620
PMCPMC4121280
OpenAlexW2064626053

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.