Evidence map›Paper›PMID 24043835›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Inositol polyphosphate multikinase is a transcriptional coactivator required for immediate early gene induction.

Risheng Xu, Bindu D Paul, Dani R Smith, Richa Tyagi, Feng Rao, A Basit Khan, Daniel J Blech, M Scott Vandiver, Maged M Harraz, Prasun Guha and 4 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Inositol polyphosphate multikinase is a metformin target that regulates cell migration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  10. Article
  11. Inositol polyphosphate multikinase mediates extinction of fear memory.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. Article
  13. TRPV1 is a physiological regulator of μ-opioid receptors.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Article
  15. Review
  16. Article
  17. 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

14 authors.

Risheng XuThe Solomon H. Snyder Department of Neuroscience, Department of Pharmacology and Molecular Sciences, and Medical Scientist Training Program, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Bindu D Paul
Dani R Smith
Richa Tyagi
Feng Rao
A Basit Khan
Daniel J Blech
M Scott Vandiver
Maged M Harraz
Prasun Guha
Ishrat Ahmed
Nilkantha Sen
Michela Gallagher
Solomon H Snyder

Funding

NEUROCHEMICAL ACTIONS OF PSYCHOTROPIC DRUGSR37MH018501 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SNYDER, SOLOMON H. · 1990 to 2009
$11.5M
NEUROCHEMICAL ACTIONS OF PSYCHOTROPIC DRUGSR01MH018501 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SNYDER, SOLOMON H. · 1985 to 2019
$10.8M
NIMH NIH HHS MH-18501NIMH NIH HHS R01 MH018501NIMH NIH HHS R37 MH018501
6 · The paper itself

Abstract

Profound induction of immediate early genes (IEGs) by neural activation is a critical determinant for plasticity in the brain, but intervening molecular signals are not well characterized. We demonstrate that inositol polyphosphate multikinase (IPMK) acts noncatalytically as a transcriptional coactivator to mediate induction of numerous IEGs. IEG induction by electroconvulsive stimulation is virtually abolished in the brains of IPMK-deleted mice, which also display deficits in spatial memory. Neural activity stimulates binding of IPMK to the histone acetyltransferase CBP and enhances its recruitment to IEG promoters. Interestingly, IPMK regulation of CBP recruitment and IEG induction does not require its catalytic activities. Dominant-negative constructs, which prevent IPMK-CBP binding, substantially decrease IEG induction. As IPMK is ubiquitously expressed, its epigenetic regulation of IEGs may influence diverse nonneural and neural biologic processes.

Indexed as

Analysis of VarianceAnimalsBrainChromatin ImmunoprecipitationCREB-Binding ProteinEpigenesis, GeneticGene Expression RegulationGenes, Immediate-EarlyMaze LearningMicePhosphotransferases (Alcohol Group Acceptor)Recognition, PsychologyTranscriptional ActivationCREB-Binding Proteininositol polyphosphate multikinasePhosphotransferases (Alcohol Group Acceptor)inositol phosphateslearning

Identifiers

PMID24043835
PMCPMC3791727

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.