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Identification of differentially expressed genes in childhood asthma

小桶 基因 Wnt信号通路 微阵列 医学 哮喘 生物标志物 DNA微阵列 DNA甲基化 甲基化 遗传学 基因表达 转录组 计算生物学 生物信息学 生物 免疫学
作者
Nian-Zhen Zhang,Xiujuan Chen,Yu-Hua Mu,Hewen Wang
出处
期刊:Medicine [Ovid Technologies (Wolters Kluwer)]
卷期号:97 (21): e10861-e10861 被引量:12
标识
DOI:10.1097/md.0000000000010861
摘要

Asthma has been the most common chronic disease in children that places a major burden for affected people and their families. An integrated analysis of microarrays studies was performed to identify differentially expressed genes (DEGs) in childhood asthma compared with normal control. We also obtained the differentially methylated genes (DMGs) in childhood asthma according to GEO. The genes that were both differentially expressed and differentially methylated were identified. Functional annotation and protein–protein interaction network construction were performed to interpret biological functions of DEGs. We performed q-RT-PCR to verify the expression of selected DEGs. One DNA methylation and 3 gene expression datasets were obtained. Four hundred forty-one DEGs and 1209 DMGs in childhood asthma were identified. Among which, 16 genes were both differentially expressed and differentially methylated in childhood asthma. Natural killer cell mediated cytotoxicity pathway, Jak-STAT signaling pathway, and Wnt signaling pathway were 3 significantly enriched pathways in childhood asthma according to our KEGG enrichment analysis. The PPI network of top 20 up- and downregulated DEGs consisted of 822 nodes and 904 edges and 2 hub proteins (UBQLN4 and MID2) were identified. The expression of 8 DEGs (GZMB, FGFBP2, CLC, TBX21, ALOX15, IL12RB2, UBQLN4) was verified by qRT-PCR and only the expression of GZMB and FGFBP2 was inconsistent with our integrated analysis. Our finding was helpful to elucidate the underlying mechanism of childhood asthma and develop new potential diagnostic biomarker and provide clues for drug design.
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