Evidence map›Paper›PMID 24693920›Full record

ArticleAmerican journal of respiratory cell and molecular biology2014

Integrative genetic analysis of allergic inflammation in the murine lung.

Samir N P Kelada, Danielle E Carpenter, David L Aylor, Peter Chines, Holly Rutledge, Elissa J Chesler, Gary A Churchill, Fernando Pardo-Manuel de Villena, David A Schwartz, Francis S Collins

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
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  4. A Long Noncoding RNA "lnc"ed to Asthma Genetics.American journal of respiratory cell and molecular biology · 2022
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  6. Review
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  11. In utero ultrafine particulate matter exposure causes offspring pulmonary immunosuppression.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. Article
  13. Article
  14. Animal models of endocrine disruption.Best practice & research. Clinical endocrinology & metabolism · 2018
    Review
  15. Identification ofGenetics · 2017
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Collaborative Cross and Diversity Outbred data resources in the Mouse Phenome Database.Mammalian genome : official journal of the International Mammalian Genome Society · 2015
    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

10 authors at 5 institutions in 1 country.

Samir N P Kelada1 National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
Danielle E Carpenter
David L Aylor
Peter Chines
Holly Rutledge
Elissa J Chesler
Gary A Churchill
Fernando Pardo-Manuel de Villena
David A Schwartz
Francis S Collins
National Institutes of Health · USJackson Laboratory · USNorth Carolina State University · USUniversity of Colorado Denver · USUniversity of North Carolina at Chapel Hill · US

Funding

UNC and PERLEGEN, IncP50GM076468 · NIGMS · JACKSON LABORATORY · PI CHURCHILL, GARY A · 2006 to 2015
$31.0M
Systems Genetic Analysis of Multi-parent CrossesR01GM070683 · NIGMS · JACKSON LABORATORY · PI BROMAN, KARL W, CHURCHILL, GARY A · 2004 to 2022
$6.8M
Modeling heterogeneity for safe cancer prevention and detectionU01CA105417 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI THREADGILL, DAVID W. · 2004 to 2013
$6.7M
Systems Genetics Resource ConsortiumU01CA134240 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI THREADGILL, DAVID W. · 2007 to 2011
$5.4M
Gene-environment interactions in asthma in mice and humansZIAHG200361 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI COLLINS, FRANCIS S. · 2009 to 2012
$2.3M
Epigenetics, environmental exposure, and reproduction in the Collaborative CrossK99ES021535 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI AYLOR, DAVID LAWRENCE · 2012 to 2013
$176k
System Genetics of Male Infertility in the Collaborative CrossF32GM090667 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI AYLOR, DAVID LAWRENCE · 2010 to 2011
$96k
Intramural NIH HHS ZIA HG200361NCI NIH HHS U01 CA105417NCI NIH HHS U01CA105417NCI NIH HHS U01 CA134240NCI NIH HHS U01CA134240NIEHS NIH HHS K99 ES021535NIGMS NIH HHS F32 GM090667NIGMS NIH HHS F32GM090667NIGMS NIH HHS GM070683NIGMS NIH HHS GM076468NIGMS NIH HHS P50 GM076468NIGMS NIH HHS R01 GM070683
6 · The paper itself

Abstract

Airway allergen exposure induces inflammation among individuals with atopy that is characterized by altered airway gene expression, elevated levels of T helper type 2 cytokines, mucus hypersecretion, and airflow obstruction. To identify the genetic determinants of the airway allergen response, we employed a systems genetics approach. We applied a house dust mite mouse model of allergic airway disease to 151 incipient lines of the Collaborative Cross, a new mouse genetic reference population, and measured serum IgE, airway eosinophilia, and gene expression in the lung. Allergen-induced serum IgE and airway eosinophilia were not correlated. We detected quantitative trait loci (QTL) for airway eosinophilia on chromosome (Chr) 11 (71.802-87.098 megabases [Mb]) and allergen-induced IgE on Chr 4 (13.950-31.660 Mb). More than 4,500 genes expressed in the lung had gene expression QTL (eQTL), the majority of which were located near the gene itself. However, we also detected approximately 1,700 trans-eQTL, and many of these trans-eQTL clustered into two regions on Chr 2. We show that one of these loci (at 147.6 Mb) is associated with the expression of more than 100 genes, and, using bioinformatics resources, fine-map this locus to a 53 kb-long interval. We also use the gene expression and eQTL data to identify a candidate gene, Tlcd2, for the eosinophil QTL. Our results demonstrate that hallmark allergic airway disease phenotypes are associated with distinct genetic loci on Chrs 4 and 11, and that gene expression in the allergically inflamed lung is controlled by both cis and trans regulatory factors.

Indexed as

AnimalsAntigens, DermatophagoidesBronchial HyperreactivityDermatophagoides pteronyssinusDisease Models, AnimalGene Expression RegulationGeneticsHypersensitivityImmunoglobulin EInflammationLungMaleMicePhenotypeQuantitative Trait LociRespiratory HypersensitivityAntigens, DermatophagoidesImmunoglobulin Eallergic airway diseasegene expression quantitative trait locisystems genetics

Identifiers

PMID24693920
PMCPMC4189492
OpenAlexW2115634760

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.