Evidence map›Paper›PMID 16899735›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2006

Calcium activation of the LMO4 transcription complex and its role in the patterning of thalamocortical connections.

Amir H Kashani, Zilong Qiu, Linda Jurata, Soo-Kyung Lee, Samuel Pfaff, Sandra Goebbels, Klaus-Armin Nave, Anirvan Ghosh

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

50 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Article
  7. How "Neuronal" Are Human Skin Mast Cells?International journal of molecular sciences · 2022
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  11. Kinase Signaling in Dendritic Development and Disease.Frontiers in cellular neuroscience · 2021
    Review
  12. Review
  13. Article
  14. Cited2 Regulates Neocortical Layer II/III Generation and Somatosensory Callosal Projection Neuron Development and Connectivity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  15. A Selective Role for Lmo4 in Cue-Reward Learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  16. Postmitotic regulation of sensory area patterning in the mammalian neocortex by Lhx2.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  17. Genetic evidence that Celsr3 and Celsr2, together with Fzd3, regulate forebrain wiring in a Vangl-independent manner.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  18. Review
  19. LMO4 is essential for paraventricular hypothalamic neuronal activity and calcium channel expression to prevent hyperphagia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  20. Review
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

8 authors at 4 institutions in 2 countries.

Amir H KashaniDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Zilong Qiu
Linda Jurata
Soo-Kyung Lee
Samuel Pfaff
Sandra Goebbels
Klaus-Armin Nave
Anirvan Ghosh
Johns Hopkins University · USMax Planck Innovation · DEMax Planck Society · DESalk Institute for Biological Studies · US

Funding

Role of CREST in Cortical Development and PlasticityR01MH068578 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SCANZIANI, MASSIMO · 2003 to 2013
$3.4M
ACTIVITY DEPENDENT REGULATION OF BDNF EXPRESSIONR01MH060598 · NIMH · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI GHOSH, ANIRVAN · 2000 to 2004
$1.3M
NIMH NIH HHS MH60598NIMH NIH HHS MH68578
6 · The paper itself

Abstract

Lasting changes in neuronal connectivity require calcium-dependent gene expression. Here we report the identification of LIM domain-only 4 (LMO4) as a mediator of calcium-dependent transcription in cortical neurons. Calcium influx via voltage-sensitive calcium channels and NMDA receptors contributes to synaptically induced LMO4-mediated transactivation. LMO4-mediated transcription is dependent on signaling via calcium/calmodulin-dependent protein (CaM) kinase IV and microtubule-associated protein (MAP) kinase downstream of synaptic stimulation. Coimmunoprecipitation experiments indicate that LMO4 can form a complex with cAMP response element-binding protein (CREB) and can interact with cofactor of LIM homeodomain protein 1 (CLIM1) and CLIM2. To evaluate the role of LMO4 in vivo, we examined the consequences of conditional loss of lmo4 in the forebrain, using the Cre-Lox gene-targeting strategy. The organization of the barrel field in somatosensory cortex is disrupted in mice in which lmo4 is deleted conditionally in the cortex. Specifically, in contrast to controls, thalamocortical afferents in conditional lmo4 null mice fail to segregate into distinct barrel-specific domains. These observations identify LMO4 as a calcium-dependent transactivator that plays a key role in patterning thalamocortical connections during development.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBody PatterningCalciumCalcium SignalingCells, CulturedCerebral CortexHomeodomain ProteinsLIM Domain ProteinsMiceNeural PathwaysRatsRats, Long-EvansThalamusTissue DistributionTranscription FactorsAdaptor Proteins, Signal TransducingCalciumHomeodomain ProteinsLIM Domain ProteinsLmo4 protein, mouseTranscription Factors

Identifiers

PMID16899735
PMCPMC6673794
OpenAlexW1979661589

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.