Evidence map›Paper›PMID 18359007›Full record

ArticleBiological psychiatry2008

Promoter variant in the GRK3 gene associated with bipolar disorder alters gene expression.

Xianjin Zhou, Thomas B Barrett, John R Kelsoe

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  6. Targeting G protein coupled receptor-related pathways as emerging molecular therapies.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2015
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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

3 authors at 2 institutions in 1 country.

Xianjin ZhouDepartment of Psychiatry, University of California, San Diego, CA 92093, USA.
Thomas B Barrett
John R Kelsoe
University of California, San Diego · USVA San Diego Healthcare System · US

Funding

ZOVIRAX CREAM TO TREAT HERPES LABIALIS IN ADOLESCENTSM01RR000827 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHANG, R JEFFREY · 1985 to 2010
$74.3M
Genomic studies of bipolar disorder and chromosome 22R01MH068503 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KELSOE, JOHN R. · 2004 to 2008
$3.1M
The Bipolar Genome StudyR01MH094483 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CRAIG, DAVID W, EDENBERG, HOWARD J · 2012 to 2014
$2.2M
COLLABORATIVE GENOMIC STUDY OF BIPOLAR DISORDERR01MH059567 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KELSOE, JOHN R. · 1998 to 2007
$1.8M
Expression of GRK3 and Association with Bipolar DisorderK08MH067959 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BARRETT, THOMAS BEACH · 2003 to 2007
$718k
Receptor desensitization defects in bipolar disorderR21MH071911 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BARRETT, THOMAS BEACH · 2004 to 2006
$573k
GENETIC LINKAGE STUDIES OF BIPOLAR AFFECTIVE DISORDERR29MH047612 · NIMH · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI KELSOE, JOHN R · 1992 to 1996
–
NCRR NIH HHS M01 RR000827NCRR NIH HHS M01 RR00827NIMH NIH HHS K08 MH067959NIMH NIH HHS MH067959NIMH NIH HHS MH071911NIMH NIH HHS MH47612NIMH NIH HHS MH59567NIMH NIH HHS MH68503NIMH NIH HHS R01 MH059567NIMH NIH HHS R01 MH068503NIMH NIH HHS R01 MH094483NIMH NIH HHS R21 MH071911
6 · The paper itself

Abstract

backgroundWe have previously reported a single nucleotide polymorphism (P-5, G-384A) in the proximal promoter of the gene for G protein receptor kinase 3 (GRK3) that was associated with bipolar disorder in two independent samples. In this study, we examined whether the G-384A variant has a functional effect on GRK3 transcription.

methodsElectrophoretic mobility shift assays were conducted using nuclear extracts from both Hela cells and adult mouse cortex. Transcriptional function was also examined using a dual luciferase reporter system transfected into in vitro human neuroblastoma cells and cultured mouse cortical neurons.

resultsThe G-384A variant abolished or reduced the formation of DNA-protein complexes using nuclear extract from both HeLa cells and adult mouse cortical neuron cells. However, gene expression was significantly enhanced by G-384A in both in vitro human neuroblastoma cells and cultured mouse cortical neurons.

conclusionsThese data suggest that the G-384A SNP in the promoter of human GRK3 gene represents an important functional variant. The G-384A variant may alter binding of Sp1/Sp4 transcription factors resulting in an increase in gene transcription and an increase in vulnerability to bipolar disorder.

Indexed as

AllelesAnimalsBipolar DisorderCell LineCell Line, TumorCerebral CortexElectrophoretic Mobility Shift AssayGene ExpressionGene Expression RegulationGenetic VariationG-Protein-Coupled Receptor Kinase 3HeLa CellsHumansMiceNeuronsPolymorphism, Single NucleotideG-Protein-Coupled Receptor Kinase 3GRK3 protein, humanSp1 Transcription FactorSP4 protein, humanSp4 Transcription Factor

Identifiers

PMID18359007
PMCPMC6528791
OpenAlexW2092232101

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.