Evidence map›Paper›PMID 24475768›Full record

ArticleJournal of neurochemistry2014

Phosphorylation of the transcription factor Sp4 is reduced by NMDA receptor signaling.

Gregory Saia, Jasmin Lalonde, Xinxin Sun, Belén Ramos, Grace Gill

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neurochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. DifferentialScience advances · 2026
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  4. Article
  5. Review
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  10. Transcription factor SP4 phosphorylation is altered in the postmortem cerebellum of bipolar disorder and schizophrenia subjects.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2015
    Article
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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

5 authors at 2 institutions in 2 countries.

Gregory SaiaDepartment of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, Massachusetts, USA; the Cell, Molecular and Developmental Biology Program, Sackler School of Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts, USA.
Jasmin Lalonde
Xinxin Sun
Belén Ramos
Grace Gill
Tufts University · USCentro de Investigación Biomédica en Red de Salud Mental · ES

Funding

Mechanisms of Neuronal Specific TranscriptionR01HD043364 · NICHD · TUFTS UNIVERSITY BOSTON · PI GILL, GRACE B · 2003 to 2009
$1.9M
Synapse Neurobiology Training ProgramT32NS061764 · NINDS · TUFTS UNIVERSITY BOSTON · PI BIEDERER, THOMAS · 2009 to 2019
$1.7M
NICHD NIH HHS R01 HD043364NINDS NIH HHS T32 NS061764
6 · The paper itself

Abstract

The regulation of transcription factor function in response to neuronal activity is important for development and function of the nervous system. The transcription factor Sp4 regulates the developmental patterning of dendrites, contributes to complex processes including learning and memory, and has been linked to psychiatric disorders such as schizophrenia and bipolar disorder. Despite its many roles in the nervous system, the molecular mechanisms regulating Sp4 activity are poorly understood. Here, we report a site of phosphorylation on Sp4 at serine 770 that is decreased in response to membrane depolarization. Inhibition of the voltage-dependent NMDA receptor increased Sp4 phosphorylation. Conversely, stimulation with NMDA reduced the levels of Sp4 phosphorylation, and this was dependent on the protein phosphatase 1/2A. A phosphomimetic substitution at S770 impaired the Sp4-dependent maturation of cerebellar granule neuron primary dendrites, whereas a non-phosphorylatable Sp4 mutant behaved like wild type. These data reveal that transcription factor Sp4 is regulated by NMDA receptor-dependent activation of a protein phosphatase 1/2A signaling pathway. Our findings also suggest that the regulated control of Sp4 activity is an important mechanism governing the developmental patterning of dendrites.

Indexed as

AnimalsCalcineurinCalcineurin InhibitorsCalcium ChannelsCell LineCerebellumDendritesDizocilpine MaleateHumansMembrane PotentialsMutagenesis, Site-DirectedNeurogenesisNeuronsN-MethylaspartateOkadaic AcidPoint MutationCalcineurinCalcineurin InhibitorsCalcium ChannelsDizocilpine MaleateN-MethylaspartateOkadaic AcidPotassium ChlorideProtein Phosphatase 1Protein Phosphatase 2Receptors, N-Methyl-D-AspartateRecombinant Fusion ProteinsRNA, Small InterferingSp4 protein, ratSp4 Transcription Factorcerebellar granule neuronsdendriteNMDA receptorphosphorylationPP1/PP2Atranscription factor Sp4

Identifiers

PMID24475768
PMCPMC3999283
OpenAlexW2075001094

What OpenQuestion holds

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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.