Evidence map›Paper›PMID 20729808›Full record

ArticleThe EMBO journal2010

A long nuclear-retained non-coding RNA regulates synaptogenesis by modulating gene expression.

Delphine Bernard, Kannanganattu V Prasanth, Vidisha Tripathi, Sabrina Colasse, Tetsuya Nakamura, Zhenyu Xuan, Michael Q Zhang, Frédéric Sedel, Laurent Jourdren, Fanny Coulpier and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 441 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
441citing papers in PubMed, 3 pooled it
14.9field-weighted citation impact, top 1% 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

441 citing papers in PubMed, 3 syntheses or guidelines pooled it, 733 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. A B1 SINE element within the mouseScience advances · 2026
    Article
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  8. Global deletion ofbioRxiv : the preprint server for biology · 2026
    Article
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  14. Intron Retention Controls Localization of lncRNAsbioRxiv : the preprint server for biology · 2026
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Molecular and Clinical Considerations for Anesthesia in the Aging Brain.International journal of molecular sciences · 2025
    Review

381 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

13 authors at 6 institutions in 3 countries.

Delphine BernardLaboratoire de Biologie Cellulaire de la Synapse, Inserm 1024/CNRS 8197, Institut de Biologie de l'Ecole Normale Supérieure, Paris, France.
Kannanganattu V Prasanth
Vidisha Tripathi
Sabrina Colasse
Tetsuya Nakamura
Zhenyu Xuan
Michael Q Zhang
Frédéric Sedel
Laurent Jourdren
Fanny Coulpier
Antoine Triller
David L Spector
Alain Bessis
Cold Spring Harbor Laboratory · USCentre National de la Recherche Scientifique · FRÉcole Normale Supérieure - PSL · FRInstitut de Biologie de l'École Normale Supérieure · FRUniversity of Illinois Urbana-Champaign · USSynapse (Netherlands) · NL

Funding

VIRAL TRANSACTIVATIONP01CA013106 · NCI · COLD SPRING HARBOR LABORATORY · PI William Richard McCombie · 1985 to 2026
$116.8M
Spatial Organization of Gene ExpressoinR01GM042694 · NIGMS · COLD SPRING HARBOR LABORATORY · PI SPECTOR, DAVID L · 1990 to 2018
$12.7M
NCI NIH HHS 5P01CA013106-38NCI NIH HHS P01 CA013106NIGMS NIH HHS R01 GM042694PHS HHS 42694
6 · The paper itself

Abstract

A growing number of long nuclear-retained non-coding RNAs (ncRNAs) have recently been described. However, few functions have been elucidated for these ncRNAs. Here, we have characterized the function of one such ncRNA, identified as metastasis-associated lung adenocarcinoma transcript 1 (Malat1). Malat1 RNA is expressed in numerous tissues and is highly abundant in neurons. It is enriched in nuclear speckles only when RNA polymerase II-dependent transcription is active. Knock-down studies revealed that Malat1 modulates the recruitment of SR family pre-mRNA-splicing factors to the transcription site of a transgene array. DNA microarray analysis in Malat1-depleted neuroblastoma cells indicates that Malat1 controls the expression of genes involved not only in nuclear processes, but also in synapse function. In cultured hippocampal neurons, knock-down of Malat1 decreases synaptic density, whereas its over-expression results in a cell-autonomous increase in synaptic density. Our results suggest that Malat1 regulates synapse formation by modulating the expression of genes involved in synapse formation and/or maintenance.

Indexed as

AnimalsBiomarkersBlotting, NorthernBone NeoplasmsCell NucleusCells, CulturedGene Expression ProfilingGene Expression RegulationHippocampusHumansMiceNeuroblastomaNeurogenesisNeuronsOligonucleotide Array Sequence AnalysisOsteosarcomaBiomarkersMta1 protein, mouseRepressor ProteinsRNA, MessengerRNA, NuclearRNA PrecursorsTrans-ActivatorsTranscription Factors

Identifiers

PMID20729808
PMCPMC2944070
OpenAlexW2111688179

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.