Evidence map›Paper›PMID 24315717›Full record

ArticleSchizophrenia research2014

Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex.

Ilaria Guella, Adolfo Sequeira, Brandi Rollins, Ling Morgan, Richard M Myers, Stanley J Watson, Huda Akil, William E Bunney, Lynn E Delisi, William Byerley and 1 more

Open access · greenAbstract read
In one paragraph

Article in Schizophrenia research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  7. Review
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  12. Recent genetic findings in schizophrenia and their therapeutic relevance.Journal of psychopharmacology (Oxford, England) · 2015
    Review
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  14. 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

11 authors at 5 institutions in 1 country.

Ilaria GuellaFunctional Genomics Laboratory, Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA.
Adolfo SequeiraFunctional Genomics Laboratory, Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA.
Brandi RollinsFunctional Genomics Laboratory, Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA.
Ling MorganFunctional Genomics Laboratory, Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA.
Richard M MyersHudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
Stanley J WatsonMolecular and Behavioral Neurosciences Institute, University of Michigan, Ann Arbor, MI, USA.
Huda AkilMolecular and Behavioral Neurosciences Institute, University of Michigan, Ann Arbor, MI, USA.
William E BunneyDepartment of Psychiatry and Human Behavior, University of California, Irvine, CA, USA.
Lynn E DelisiHarvard Medical School, Brockton VA Boston Healthcare System, Brockton, MA, USA.
William ByerleyDepartment of Psychiatry, University of California, San Francisco, CA, USA.
Marquis P VawterFunctional Genomics Laboratory, Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA. Electronic address: mvawter@uci.edu.
University of California, Irvine · USNeurosciences Institute · USHudsonAlpha Institute for Biotechnology · USSignature Healthcare Brockton Hospital · USUniversity of California, San Francisco · US

Funding

Genomic Psychiatry CohortR01MH085548 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PATO, CARLOS N, PATO, MICHELE T · 2008 to 2012
$16.3M
Mitochondrial Dysfunction In SchizophreniaR01MH085801 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI VAWTER, MARQUIS PHILIP · 2009 to 2020
$5.0M
Mitochondrial Deletions in Mood DisordersR21MH099440 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI VAWTER, MARQUIS PHILIP · 2013 to 2014
$424k
NIMH NIH HHS R01MH08554NIMH NIH HHS R01 MH085548NIMH NIH HHS R01 MH085801NIMH NIH HHS R01MH085801NIMH NIH HHS R01MH 099440NIMH NIH HHS R21 MH099440
6 · The paper itself

Abstract

The rs1344706, an intronic SNP within the zinc-finger protein 804A gene (ZNF804A), was identified as one of the most compelling risk SNPs for schizophrenia (SZ) and bipolar disorder (BD). It is however not clear by which molecular mechanisms ZNF804A increases disease risk. We evaluated the role of ZNF804A in SZ and BD by genotyping the originally associated rs1344706 SNP and an exonic SNP (rs12476147) located in exon four of ZNF804A in a sample of 422 SZ, 382 BD, and 507 controls from the isolated population of the Costa Rica Central Valley. We also investigated the rs1344706 SNP for allelic specific expression (ASE) imbalance in the dorsolateral prefrontal cortex (DLPFC) of 46 heterozygous postmortem brains. While no significant association between rs1344706 and SZ or BD was observed in the Costa Rica sample, we observed an increased risk of SZ for the minor allele (A) of the exonic rs12476147 SNP (p=0.026). Our ASE assay detected a significant over-expression of the rs12476147 A allele in DLPFC of rs1344706 heterozygous subjects. Interestingly, cDNA allele ratios were significantly different according to the intronic rs1344706 genotypes (p-value=0.03), with the rs1344706 A allele associated with increased ZNF804A rs12476147 A allele expression (average 1.06, p-value=0.02, for heterozygous subjects vs. genomic DNA). In conclusion, we have demonstrated a significant association of rs12476147 with SZ, and using a powerful within-subject design, an allelic expression imbalance of ZNF804A exonic SNP rs12476147 in the DLPFC. Although this data does not preclude the possibility of other functional variants in ZNF804A, it provides evidence that the rs1344706 SZ risk allele is the cis-regulatory variant directly responsible for this allelic expression imbalance in adult cortex.

Indexed as

Allelic ImbalanceBipolar DisorderCohort StudiesCosta RicaFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansKruppel-Like Transcription FactorsMalePolymorphism, Single NucleotidePostmortem ChangesPrefrontal CortexSchizophreniaKruppel-Like Transcription FactorsZNF804A protein, humanAllelic-specific expressionAssociation studyBipolar disorderrs1344706SchizophreniaZNF804A

Identifiers

PMID24315717
PMCPMC3947280
OpenAlexW2106711891

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.