Evidence map›Paper›PMID 25874939›Full record

ArticlePLoS genetics2015

Host genetic variation influences gene expression response to rhinovirus infection.

Minal Çalışkan, Samuel W Baker, Yoav Gilad, Carole Ober

Abstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

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

  1. Pooled it
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  14. bioRxiv : the preprint server for biology · 2023
    Article
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  19. Gene-environment interactions in childhood asthma revisited; expanding the interaction concept.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2022
    Review
  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

4 authors.

Minal ÇalışkanDepartment of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Samuel W BakerDepartment of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Yoav GiladDepartment of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Carole OberDepartment of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.

Funding

Virus-Bacterial Interactions and Exacerba of AsthmaP01HL070831 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI GANGNON, RONALD E · 2002 to 2017
$31.3M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Regulation and expression of HLA-G in asthmatic airwaysU19AI095230 · NIAID · UNIVERSITY OF CHICAGO · PI SPERLING, ANNE I. · 2011 to 2016
$10.5M
Systems Genetics Approach to Gene Discovery in Chronic RhinosinusitisU19AI106683 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHLEIMER, ROBERT P · 2014 to 2017
$7.9M
Sex-Specific Genetic Architecture of Asthma-Associated Quantitative TraitsR01HL085197 · NHLBI · UNIVERSITY OF CHICAGO · PI OBER, CAROLE · 2007 to 2015
$7.6M
Analysis and interpretation of noncoding regulatory variationR01MH084703 · NIMH · UNIVERSITY OF CHICAGO · PI GILAD, YOAV, PRITCHARD, JONATHAN K · 2008 to 2015
$3.4M
Systems Genetics Approach to Gene Discovery in Chronic RhinosinusitisP01AI106683 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHLEIMER, ROBERT P · 2013 to 2013
$1.7M
NCATS NIH HHS UL1 TR000430NHLBI NIH HHS P01 HL070831NHLBI NIH HHS R01 HL085197NIAID NIH HHS P01 AI106683NIAID NIH HHS U19 AI095230NIAID NIH HHS U19 AI106683NIMH NIH HHS R01 MH084703
6 · The paper itself

Abstract

Rhinovirus (RV) is the most prevalent human respiratory virus and is responsible for at least half of all common colds. RV infections may result in a broad spectrum of effects that range from asymptomatic infections to severe lower respiratory illnesses. The basis for inter-individual variation in the response to RV infection is not well understood. In this study, we explored whether host genetic variation is associated with variation in gene expression response to RV infections between individuals. To do so, we obtained genome-wide genotype and gene expression data in uninfected and RV-infected peripheral blood mononuclear cells (PBMCs) from 98 individuals. We mapped local and distant genetic variation that is associated with inter-individual differences in gene expression levels (eQTLs) in both uninfected and RV-infected cells. We focused specifically on response eQTLs (reQTLs), namely, genetic associations with inter-individual variation in gene expression response to RV infection. We identified local reQTLs for 38 genes, including genes with known functions in viral response (UBA7, OAS1, IRF5) and genes that have been associated with immune and RV-related diseases (e.g., ITGA2, MSR1, GSTM3). The putative regulatory regions of genes with reQTLs were enriched for binding sites of virus-activated STAT2, highlighting the role of condition-specific transcription factors in genotype-by-environment interactions. Overall, we suggest that the 38 loci associated with inter-individual variation in gene expression response to RV-infection represent promising candidates for affecting immune and RV-related respiratory diseases.

Indexed as

Genetic LociGenetic VariationTranscriptome2',5'-Oligoadenylate SynthetaseAdultCommon ColdFemaleGene-Environment InteractionGene Expression ProfilingGlutathione TransferaseHumansIntegrin alpha2Interferon Regulatory FactorsLeukocytes, MononuclearMaleMiddle Aged2',5'-Oligoadenylate SynthetaseGlutathione TransferaseGSTM3 protein, humanIntegrin alpha2Interferon Regulatory FactorsIRF5 protein, humanITGA2B protein, humanMSR1 protein, humanOAS1 protein, humanScavenger Receptors, Class ASTAT2 protein, humanSTAT2 Transcription Factor

Identifiers

PMID25874939
PMCPMC4395341

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.