Evidence map›Paper›PMID 24155305›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Deletion of CPEB3 enhances hippocampus-dependent memory via increasing expressions of PSD95 and NMDA receptors.

Hsu-Wen Chao, Li-Yun Tsai, Yi-Ling Lu, Pei-Yi Lin, Wen-Hsuan Huang, Hsin-Jung Chou, Wen-Hsin Lu, Hsiu-Chen Lin, Ping-Tao Lee, Yi-Shuian Huang

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

52 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Role of CPEBs in Learning and Memory.Journal of neurochemistry · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
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  11. Inhibition ofeLife · 2024
    Article
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  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. RNA-binding protein signaling in adult neurogenesis.Frontiers in cell and developmental biology · 2022
    Review
  19. Article
  20. CPEB3-dowregulated Nr3c1 mRNA translation confers resilience to developing posttraumatic stress disorder-like behavior in fear-conditioned mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
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

10 authors at 2 institutions in 1 country.

Hsu-Wen ChaoInstitute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan and Taiwan International Graduate Program, National Yang-Ming University, Taipei 112, Taiwan.
Li-Yun Tsai
Yi-Ling Lu
Pei-Yi Lin
Wen-Hsuan Huang
Hsin-Jung Chou
Wen-Hsin Lu
Hsiu-Chen Lin
Ping-Tao Lee
Yi-Shuian Huang
Institute of Biomedical Sciences, Academia Sinica · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term memory requires activity-dependent synthesis of plasticity-related proteins (PRPs) to strengthen synaptic efficacy and consequently consolidate memory. Cytoplasmic polyadenylation element binding protein (CPEB)3 is a sequence-specific RNA-binding protein that regulates translation of several PRP RNAs in neurons. To understand whether CPEB3 plays a part in learning and memory, we generated CPEB3 knock-out (KO) mice and found that the null mice exhibited enhanced hippocampus-dependent, short-term fear memory in the contextual fear conditioning test and long-term spatial memory in the Morris water maze. The basal synaptic transmission of Schaffer collateral-CA1 neurons was normal but long-term depression evoked by paired-pulse low-frequency stimulation was modestly facilitated in the juvenile KO mice. Molecular and cellular characterizations revealed several molecules in regulating plasticity of glutamatergic synapses are translationally elevated in the CPEB3 KO neurons, including the scaffolding protein PSD95 and the NMDA receptors along with the known CPEB3 target, GluA1. Together, CPEB3 functions as a negative regulator to confine the strength of glutamatergic synapses by downregulating the expression of multiple PRPs and plays a role underlying certain forms of hippocampus-dependent memories.

Indexed as

Memory, Short-TermAnimalsConditioning, ClassicalDisks Large Homolog 4 ProteinFearGuanylate KinasesHippocampusLong-Term Synaptic DepressionMaze LearningMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutNeuronsReceptors, AMPAReceptors, N-Methyl-D-AspartateCpeb3 protein, mouseDisks Large Homolog 4 ProteinDlg4 protein, mouseGuanylate KinasesMembrane ProteinsReceptors, AMPAReceptors, N-Methyl-D-AspartateRNA-Binding Proteins

Identifiers

PMID24155305
PMCPMC6618447
OpenAlexW2085163415

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.