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pmid:30868055

Genome-wide profiling of mRNA and lncRNA expression in dengue fever and dengue hemorrhagic fever.

Xiao-Lan Zhong · Xiao-Ming Liao · Fei Shen · Hai-Jian Yu · Wen-Sheng Yan · Yun-Fang Zhang · Jia-Jun Ye · Zhi-Ping Lv

FEBS open bio · 2019 doi:10.1002/2211-5463.12576

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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title
Genome-wide profiling of mRNA and lncRNA expression in dengue fever and dengue hemorrhagic fever.
doi
10.1002/2211-5463.12576
pmid
30868055
authors array · 8 items
[0]
Xiao-Lan Zhong
[1]
Xiao-Ming Liao
[2]
Fei Shen
[3]
Hai-Jian Yu
[4]
Wen-Sheng Yan
[5]
Yun-Fang Zhang
[6]
Jia-Jun Ye
[7]
Zhi-Ping Lv
journal
FEBS open bio
year
2019
abstract
Dengue fever (DF) and dengue hemorrhagic fever (DHF) are recurrent diseases that are widespread in the tropics. Here, we identified candidate genes associated with these diseases by performing integrated analyses of DF (GSE51808) and DHF (GSE18090) microarray datasets in the Gene Expression Omnibus (GEO). In all, we identified 7635 differentially expressed genes (DEGs) in DF and 8147 DEGs in DHF as compared to healthy controls (P < 0.05). In addition, we discovered 215 differentially expressed long non-coding RNAs (DElncRNAs) in DF and 225 DElncRNAs in DHF. There were 1256 common DEGs and eight common DElncRNAs in DHF vs DF, DHF vs normal control, and DF vs normal control groups. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed that signal transduction (false discovery rate = 8.33E-10), 'toxoplasmosis', and 'protein processing in endoplasmic reticulum' were significantly enriched pathways for common DEGs. We conclude that the MAGED1,STAT1, and IL12A genes may play crucial roles in DF and DHF, and suggest that our findings may facilitate the identification of biomarkers and the development of new drug design strategies for DF and DHF treatment.
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sections[7] "Identification of common differentially expressed mRNAs and lncRNAs in the comparisons of DF vs normal control, DHF vs normal control, and DF vs DHF" paragraph 2
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The Wilcoxon rank‐sum test was used to identify significant differences in the expression of mRNAs and lncRNAs between the different groups.
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Here, we identified candidate genes associated with these diseases by performing integrated analyses of DF (GSE51808) and DHF (GSE18090) microarray datasets in the Gene Expression Omnibus (GEO).
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Gene Expression Profiling During Early Acute Febrile Stage of Dengue Infection Can Predict The Disease Outcome
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Proximity analysis of DElncRNA‐DEmRNA
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agent:corpus-assay-engine
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The Wilcoxon rank‐sum test was used to identify significant differences in the expression of mRNAs and lncRNAs between the different groups.
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Complete file
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Here, we identified candidate genes associated with these diseases by performing integrated analyses of DF (GSE51808) and DHF (GSE18090) microarray datasets in the Gene Expression Omnibus (GEO). In all, we identified 7635 differentially expressed genes (DEGs) in DF and 8147 DEGs in DHF as compared to healthy controls (P < 0.05). In addition, we discovered 215 differentially expressed long non-coding RNAs (DElncRNAs) in DF and 225 DElncRNAs in DHF. There were 1256 common DEGs and eight common DElncRNAs in DHF vs DF, DHF vs normal control, and DF vs normal control groups. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed that signal transduction (false discovery rate = 8.33E-10), 'toxoplasmosis', and 'protein processing in endoplasmic reticulum' were significantly enriched pathways for common DEGs. 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