Evidence map›Paper›PMID 22069327›Full record

ArticleThe Journal of biological chemistry2012

Direct interaction between scaffolding proteins RACK1 and 14-3-3ζ regulates brain-derived neurotrophic factor (BDNF) transcription.

Jérémie Neasta, Patrick A Kiely, Dao-Yao He, David R Adams, Rosemary O'Connor, Dorit Ron

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  7. Growth Factors and Alcohol Use Disorder.Cold Spring Harbor perspectives in medicine · 2020
    Review
  8. The mitochondrial metabolic function ofFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
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  13. The First Alcohol Drink Triggers mTORC1-Dependent Synaptic Plasticity in Nucleus Accumbens Dopamine D1 Receptor Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    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

6 authors at 4 institutions in 3 countries.

Jérémie NeastaErnest Gallo Research Center, Department of Neurology, University of California, San Francisco, Emeryville, California 94608.
Patrick A KielyCell Biology Laboratory, Department of Biochemistry, BioSciences Institute, University College Cork, Cork, Ireland.
Dao-Yao HeErnest Gallo Research Center, Department of Neurology, University of California, San Francisco, Emeryville, California 94608.
David R AdamsDepartment of Chemistry, Heriot-Watt University, Riccarton Campus, Edinburgh EH14AS, Scotland, United Kingdom.
Rosemary O'ConnorCell Biology Laboratory, Department of Biochemistry, BioSciences Institute, University College Cork, Cork, Ireland.
Dorit RonErnest Gallo Research Center, Department of Neurology, University of California, San Francisco, Emeryville, California 94608. Electronic address: dron@gallo.ucsf.edu.
Ernest Gallo Clinic and Research Center · USUniversity College Cork · IEHeriot-Watt University · GBUniversity of California, San Francisco · US

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jennifer Leigh Clarke · 1999 to 2026
$209.7M
BDNF and Alcohol AddictionR01AA016848 · NIAAA · ERNEST GALLO CLINIC AND RESEARCH CENTER · PI RON, DORIT · 2008 to 2012
$1.8M
NCI NIH HHS P30 CA082103NIAAA NIH HHS R01 AA016848
6 · The paper itself

Abstract

RACK1 is a scaffolding protein that spatially and temporally regulates numerous signaling cascades. We previously found that activation of the cAMP signaling pathway induces the translocation of RACK1 to the nucleus. We further showed that nuclear RACK1 is required to promote the transcription of the brain-derived neurotrophic factor (BDNF). Here, we set out to elucidate the mechanism underlying cAMP-dependent RACK1 nuclear translocation and BDNF transcription. We identified the scaffolding protein 14-3-3ζ as a direct binding partner of RACK1. Moreover, we found that 14-3-3ζ was necessary for the cAMP-dependent translocation of RACK1 to the nucleus. We further observed that the disruption of RACK1/14-3-3ζ interaction with a peptide derived from the RACK1/14-3-3ζ binding site or shRNA-mediated 14-3-3ζ knockdown inhibited cAMP induction of BDNF transcription. Together, these data reveal that the function of nuclear RACK1 is mediated through its interaction with 14-3-3ζ. As RACK1 and 14-3-3ζ are two multifunctional scaffolding proteins that coordinate a wide variety of signaling events, their interaction is likely to regulate other essential cellular functions.

Indexed as

Gene Expression RegulationTranscription, Genetic14-3-3 ProteinsActive Transport, Cell NucleusAmino Acid SequenceAnimalsBrain-Derived Neurotrophic FactorCell Line, TumorCell NucleusCyclic AMPCyclic AMP-Dependent Protein KinasesGTP-Binding ProteinsHumansModels, MolecularMolecular Sequence DataNeoplasm Proteins14-3-3 ProteinsBrain-Derived Neurotrophic FactorCyclic AMPCyclic AMP-Dependent Protein KinasesGTP-Binding ProteinsNeoplasm ProteinsRACK1 protein, humanRACK1 protein, ratReceptors, Cell SurfaceReceptors for Activated C Kinase

Identifiers

PMID22069327
PMCPMC3249084
OpenAlexW2012112040

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.