Evidence map›Paper›PMID 24045843›Full record

ArticleEuropean journal of human genetics : EJHG2014

Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1.

Belinda J Kaskow, Luke A Diepeveen, J Michael Proffitt, Alexander J Rea, Daniela Ulgiati, John Blangero, Eric K Moses, Lawrence J Abraham

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

8 authors.

Belinda J KaskowSchool of Chemistry and Biochemistry, University of Western Australia, Crawley, WA, Australia.
Luke A DiepeveenSchool of Chemistry and Biochemistry, University of Western Australia, Crawley, WA, Australia.
J Michael ProffittDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
Alexander J ReaSchool of Chemistry and Biochemistry, University of Western Australia, Crawley, WA, Australia.
Daniela UlgiatiSchool of Chemistry and Biochemistry, University of Western Australia, Crawley, WA, Australia.
John BlangeroDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
Eric K MosesCentre for Genetic Origins of Health and Disease (GOHaD), University of Western Australia, Crawley, WA, Australia.
Lawrence J Abraham1] School of Chemistry and Biochemistry, University of Western Australia, Crawley, WA, Australia [2] Centre for Genetic Origins of Health and Disease (GOHaD), University of Western Australia, Crawley, WA, Australia.

Funding

PEDIGREE ANALYSIS OF LIPOPROTEIN PHENOTYPESP01HL045522 · NHLBI · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 1991 to 2012
$27.6M
Integrative Genomics of Vanin Gene Expression in Relation to CVD RiskR01HL093537 · NHLBI · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI ABRAHAM, LAWRENCE JOSEPH, BLANGERO, JOHN · 2010 to 2013
$2.0M
NHLBI NIH HHS HL93537NHLBI NIH HHS P01 HL045522NHLBI NIH HHS R01 HL093537
6 · The paper itself

Abstract

There is now good evidence that non-coding sequence variants are involved in the heritability of many common complex traits. The current 'gold standard' approach for assessing functionality is the in vitro reporter gene assay to assess allelic differences in transcriptional activity, usually followed by electrophoretic mobility shift assays to assess allelic differences in transcription factor binding. Although widely used, these assays have inherent limitations, including the lack of endogenous chromatin context. Here we present a more contemporary approach to assessing functionality of non-coding sequence variation within the Vanin-1 (VNN1) promoter. By combining 'gold standard' assays with in vivo assessments of chromatin accessibility, we greatly increase our confidence in the statistically assigned functional relevance. The standard assays revealed the -137 single nucleotide variant to be functional but the -587 variant to have no functional relevance. However, our in vivo tests show an allelic difference in chromatin accessibility surrounding the -587 variant supporting strong functional potential at both sites. Our approach advances the identification of functional variants by providing strong in vivo biological evidence for function.

Indexed as

Gene Expression RegulationGenetic VariationQuantitative Trait LociAllelesAmidohydrolasesBase SequenceCardiovascular DiseasesChromatinDNA MethylationGenes, ReporterGPI-Linked ProteinsHumansMolecular Sequence DataPolymorphism, Single NucleotidePromoter Regions, GeneticAmidohydrolasesChromatinGPI-Linked Proteinspantetheinase

Identifiers

PMID24045843
PMCPMC3992570

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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.