Evidence map›Paper›PMID 20371816›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

LEF1/beta-catenin complex regulates transcription of the Cav3.1 calcium channel gene (Cacna1g) in thalamic neurons of the adult brain.

Marta B Wisniewska, Katarzyna Misztal, Wojciech Michowski, Marcin Szczot, Elzbieta Purta, Wieslawa Lesniak, Monika E Klejman, Michal Dabrowski, Robert K Filipkowski, Andrzej Nagalski and 2 more

Abstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
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

41 citing papers in PubMed.

  1. Article
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  6. Review
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  9. Article
  10. WNT Signaling Is a Key Player in Alzheimer's Disease.Handbook of experimental pharmacology · 2021
    Article
  11. Article
  12. Dynamic Expression Profiles of β-Catenin during Murine Cardiac Valve Development.Journal of cardiovascular development and disease · 2020
    Article
  13. Article
  14. High-Throughput Data Reveals Novel Circular RNAs via Competitive Endogenous RNA Networks Associated with Human Intracranial Aneurysms.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  15. Article
  16. Review
  17. Screening of Potential Genes and Transcription Factors of Postoperative Cognitive Dysfunction via Bioinformatics Methods.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  18. Article
  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

12 authors.

Marta B WisniewskaInternational Institute of Molecular and Cell Biology, 02-109 Warsaw, Poland. mwisniew@iimcb.gov.pl
Katarzyna Misztal
Wojciech Michowski
Marcin Szczot
Elzbieta Purta
Wieslawa Lesniak
Monika E Klejman
Michal Dabrowski
Robert K Filipkowski
Andrzej Nagalski
Jerzy W Mozrzymas
Jacek Kuznicki

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

beta-Catenin, together with LEF1/TCF transcription factors, activates genes involved in the proliferation and differentiation of neuronal precursor cells. In mature neurons, beta-catenin participates in dendritogenesis and synaptic function as a component of the cadherin cell adhesion complex. However, the transcriptional activity of beta-catenin in these cells remains elusive. In the present study, we found that in the adult mouse brain, beta-catenin and LEF1 accumulate in the nuclei of neurons specifically in the thalamus. The particular electrophysiological properties of thalamic neurons depend on T-type calcium channels. Cav3.1 is the predominant T-type channel subunit in the thalamus, and we hypothesized that the Cacna1g gene encoding Cav3.1 is a target of the LEF1/beta-catenin complex. We demonstrated that the expression of Cacna1g is high in the thalamus and is further increased in thalamic neurons treated in vitro with LiCl or WNT3A, activators of beta-catenin. Luciferase reporter assays confirmed that the Cacna1G promoter is activated by LEF1 and beta-catenin, and footprinting analysis revealed four LEF1 binding sites in the proximal region of this promoter. Chromatin immunoprecipitation demonstrated that the Cacna1g proximal promoter is occupied by beta-catenin in vivo in the thalamus, but not in the hippocampus. Moreover, WNT3A stimulation enhanced T-type current in cultured thalamic neurons. Together, our data indicate that the LEF1/beta-catenin complex regulates transcription of Cacna1g and uncover a novel function for beta-catenin in mature neurons. We propose that beta-catenin contributes to neuronal excitability not only by a local action at the synapse but also by activating gene expression in thalamic neurons.

Indexed as

Age FactorsAnimalsbeta CateninCalcium Channels, T-TypeCells, CulturedFemaleHeLa CellsHumansLymphoid Enhancer-Binding Factor 1MaleMiceNeuronsRatsSynapsesThalamusTranscriptional Activationbeta CateninCacna1g protein, mouseCalcium Channels, T-TypeCTNNB1 protein, mouseLef1 protein, mouseLymphoid Enhancer-Binding Factor 1

Identifiers

PMID20371816
PMCPMC6632775

What OpenQuestion holds

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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.