Detection of lncRNA-mRNA interaction modules by integrating eQTL with weighted gene co-expression network analysis

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作者
Xing-Bo Mo
Long-Fei Wu
Xin Lu
Xiao-Wei Zhu
Wei Xia
Lan Wang
Pei He
Peng-Fei Bing
Yong-Hong Zhang
Fei-Yan Deng
Shu-Feng Lei
机构
[1] Medical College of Soochow University,Center for Genetic Epidemiology and Genomics, School of Public Health
[2] Soochow University,Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases
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关键词
Long noncoding RNA; eQTL; Weighted gene co-expression network analysis; Functional annotation; HOTAIR;
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摘要
One major function of lncRNA is to regulate the expression of mRNA, but the patterns of their interactions were largely unknown. We attempted to construct lncRNA-mRNA interaction modules at a genome-wide scale. We performed a genome-wide lncRNA-mRNA eQTL analysis in peripheral blood mononuclear cells of 43 individuals, followed by weighted gene co-expression network analysis and functional enrichment analysis which sought to detect functional modules. There were 4627 significant cis lnc-eQTL pairs (P < 1.4 × 10−6) and 1,587,128 significant trans lnc-eQTL pairs (P < 3.46 × 10−9). We detected 11 eQTL modules for the lnc-eQTL networks. Among them, five modules showed significant enrichments in GO terms, and three modules showed significant enrichments in specific KEGG pathways (e.g., Toll-like receptor, PI3K-Akt, NF-kappa B, and TNF signaling pathways). lncRNA-protein interaction analysis showed that some well-known functional lncRNAs (HOTAIR, CCDC26, RHPN1-AS1, WT1-AS, and TCL6) in the eQTL module interacted with genes in focal adhesion and PI3K-Akt signaling pathway. We identified biologically functional lncRNA-mRNA interaction modules by integrating eQTL and weighted gene co-expression network analysis. Integrative analysis of lncRNA and mRNA data by applying eQTL analysis and weighted gene co-expression network analysis methods could be helpful for functional annotation of lncRNAs.
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页码:217 / 225
页数:8
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