dedup_wf_001--102a19d2085c3f7ffe3979016a640785

Objective: Genome-wide association studies (GWASs) have identified genes associated with asthma, however expression of these genes in asthma-relevant tissues has not been studied. This study tested expression and correlation between GWAS-identified asthma genes and asthma or asthma severity. Methods: Correlation analyses of expression levels of GWAS-identified asthma genes and asthma-related biomarkers were performed in cells from human bronchial epithelial biopsy (BEC, n = 107) and bronchial alveolar lavage (BAL, n = 94). Results: Expression levels of asthma genes between BEC and BAL and with asthma or asthma severity were weakly correlated. The expression levels of IL18R1 were consistently higher in asthma than controls or in severe asthma than mild/moderate asthma in BEC and BAL (p < 0.05). In RAD50-IL13 region, the expression levels of RAD50, not IL4, IL5, or IL13, were positively correlated between BEC and BAL (ρ = 0.53, P = 4.5 × 10−6). The expression levels of IL13 were positively correlated with IL5 in BEC (ρ = 0.35, P = 1.9 × 10−4) and IL4 in BAL (ρ = 0.42, P = 2.5 × 10−5), respectively. rs3798134 in RAD50, a GWAS-identified SNP, was correlated with IL13 expression and the expression levels of IL13 were correlated with asthma (P = 0.03). rs17772583 in RAD50 was significantly correlated with RAD50 expression in BAL and BEC (P = 7.4 × 10−7 and 0.04) but was not associated with asthma. Conclusions: This is the first report studying the expression of GWAS-identified asthma genes in BEC and BAL. IL13, rather than RAD50, IL4, or IL5, is more likely to be the asthma susceptibility gene. Our study illustrates tissue-specific expression of asthma-related genes. Therefore, whenever possible, disease-relevant tissues should be used for transcription analysis.

Tags
Data and Resources
To access the resources you must log in

This item has no data

Identity

Description: The Identity category includes attributes that support the identification of the resource.

Field Value
PID https://www.doi.org/10.6084/m9.figshare.3159676
PID https://www.doi.org/10.6084/m9.figshare.3159676.v1
PID https://www.doi.org/10.3109/02770903.2016.1158268
PID pmid:27050946
PID pmc:PMC5137190
URL http://dx.doi.org/10.6084/m9.figshare.3159676.v1
URL https://dx.doi.org/10.6084/m9.figshare.3159676.v1
URL https://europepmc.org/articles/PMC5137190/
URL http://dx.doi.org/10.6084/m9.figshare.3159676
Access Modality

Description: The Access Modality category includes attributes that report the modality of exploitation of the resource.

Field Value
Access Right Open Access
Attribution

Description: Authorships and contributors

Field Value
Author Xingnan Li
Author Hawkins, Gregory A.
Author Moore, Wendy C.
Author Hastie, Annette T.
Author Ampleford, Elizabeth J.
Author Milosevic, Jadranka
Author Huashi Li
Author Busse, William W.
Author Erzurum, Serpil C.
Author Kaminski, Naftali
Author Wenzel, Sally E.
Author Bleecker, Eugene R.
Author Meyers, Deborah A.
Publishing

Description: Attributes about the publishing venue (e.g. journal) and deposit location (e.g. repository)

Field Value
Collected From Europe PubMed Central; PubMed Central; figshare; Datacite; Crossref
Hosted By Europe PubMed Central; figshare
Publication Date 2016-04-06
Additional Info
Field Value
Language UNKNOWN
Resource Type Other literature type; UNKNOWN
keyword FOS: Mathematics
keyword FOS: Health sciences
keyword FOS: Biological sciences
keyword FOS: Clinical medicine
system:type publication
Management Info
Field Value
Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::102a19d2085c3f7ffe3979016a640785
Author jsonws_user
Last Updated 25 December 2020, 17:54 (CET)
Created 25 December 2020, 17:54 (CET)