Evidence map›Paper›PMID 24366545›Full record

ArticleMolecular and cellular biology2014

DREAM controls the on/off switch of specific activity-dependent transcription pathways.

Britt Mellström, Ignasi Sahún, Ana Ruiz-Nuño, Patricia Murtra, Rosa Gomez-Villafuertes, Magali Savignac, Juan C Oliveros, Paz Gonzalez, Asta Kastanauskaite, Shira Knafo and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 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
1.7field-weighted citation impact, top 18% 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, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Enhancement of physiology via adaptive transcription.Pflugers Archiv : European journal of physiology · 2025
    Review
  4. Review
  5. Article
  6. KCells · 2023
    Review
  7. Emerging Role of DREAM in Healthy Brain and Neurological Diseases.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Global Gene Knockout ofFrontiers in molecular neuroscience · 2019
    Article
  14. Article
  15. CaFrontiers in molecular neuroscience · 2018
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

19 authors at 8 institutions in 4 countries.

Britt MellströmNational Center of Biotechnology, CSIC and CIBERNED, Madrid, Spain.
Ignasi Sahún
Ana Ruiz-Nuño
Patricia Murtra
Rosa Gomez-Villafuertes
Magali Savignac
Juan C Oliveros
Paz Gonzalez
Asta Kastanauskaite
Shira Knafo
Min Zhuo
Alejandro Higuera-Matas
Michael L Errington
Rafael Maldonado
Javier DeFelipe
John G R Jefferys
Tim V P Bliss
Mara Dierssen
Jose R Naranjo
Biomedical Research Networking Center on Neurodegenerative Diseases · ESCentro Nacional de Biotecnología · ESInstituto Cajal · ESPompeu Fabra University · ESUniversity of Birmingham · GBCentre for Biomedical Network Research on Rare Diseases · ESCentre for Genomic Regulation · ESSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Changes in nuclear Ca(2+) homeostasis activate specific gene expression programs and are central to the acquisition and storage of information in the brain. DREAM (downstream regulatory element antagonist modulator), also known as calsenilin/KChIP-3 (K(+) channel interacting protein 3), is a Ca(2+)-binding protein that binds DNA and represses transcription in a Ca(2+)-dependent manner. To study the function of DREAM in the brain, we used transgenic mice expressing a Ca(2+)-insensitive/CREB-independent dominant active mutant DREAM (daDREAM). Using genome-wide analysis, we show that DREAM regulates the expression of specific activity-dependent transcription factors in the hippocampus, including Npas4, Nr4a1, Mef2c, JunB, and c-Fos. Furthermore, DREAM regulates its own expression, establishing an autoinhibitory feedback loop to terminate activity-dependent transcription. Ablation of DREAM does not modify activity-dependent transcription because of gene compensation by the other KChIP family members. The expression of daDREAM in the forebrain resulted in a complex phenotype characterized by loss of recurrent inhibition and enhanced long-term potentiation (LTP) in the dentate gyrus and impaired learning and memory. Our results indicate that DREAM is a major master switch transcription factor that regulates the on/off status of specific activity-dependent gene expression programs that control synaptic plasticity, learning, and memory.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCalciumCells, CulturedCyclic AMP Response Element-Binding ProteinDentate GyrusDown-RegulationGABAergic NeuronsHippocampusKv Channel-Interacting ProteinsLearningMiceMice, TransgenicPromoter Regions, GeneticProsencephalonRepressor ProteinsBasic Helix-Loop-Helix ProteinsCalciumCreb1 protein, mouseCsen protein, mouseCyclic AMP Response Element-Binding ProteinKv Channel-Interacting ProteinsNpas4 protein, mouseRepressor ProteinsTranscription Factors

Identifiers

PMID24366545
PMCPMC4023831
OpenAlexW2115685783

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.