Comprehensive circRNA-microRNA-mRNA network analysis revealed the novel regulatory mechanism of Trichosporon asahii infection
Autor: | Xin Yang, Rongya Yang, Wan-Ting Luo, Zhi-Hong Zhu, Mingwang Zhang, Zhikuan Xia, Junhong Ao |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Leukocyte migration Trichosporon asahii 03 medical and health sciences 0302 clinical medicine Circular RNA Trichosporonosis microRNA Humans Medicine RNA Messenger KEGG Genetics lcsh:R5-920 lcsh:Military Science Competing endogenous RNA business.industry Basidiomycota lcsh:U Research RNA RNA sequencing RNA Circular General Medicine Non-coding RNA MicroRNAs 030104 developmental biology 030220 oncology & carcinogenesis lcsh:Medicine (General) business Signal Transduction |
Zdroj: | Military Medical Research Military Medical Research, Vol 8, Iss 1, Pp 1-11 (2021) |
ISSN: | 2054-9369 2095-7467 |
Popis: | Background Invasive Trichosporon asahii (T. asahii) infection frequently occurs with a high mortality in immunodeficient hosts, but the pathogenesis of T. asahii infection remains elusive. Circular RNAs (circRNAs) are a type of endogenous noncoding RNA that participate in various disease processes. However, the mechanism of circRNAs in T. asahii infection remains completely unknown. Methods RNA sequencing (RNA-seq) was performed to analyze the expression profiles of circRNAs, microRNAs (miRNAs), and mRNAs in THP-1 cells infected with T. asahii or uninfected samples. Some of the RNA-seq results were verified by RT-qPCR. Gene Ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were used to analyze the differentially expressed mRNAs. A circRNA-miRNA-mRNA network was constructed and verified by dual-luciferase reporter assay and overexpression experiments. Results A total of 46 circRNAs, 412 mRNAs and 47 miRNAs were differentially expressed at 12 h after T. asahii infection. GO and KEGG analyses showed that the differentially expressed mRNAs were primarily linked to the leukocyte migration involved in the inflammatory response, the Toll-like receptor signaling pathway, and the TNF signaling pathway. A competing endogenous RNA (ceRNA) network was constructed with 5 differentially expressed circRNAs, 5 differentially expressed miRNAs and 42 differentially expressed mRNAs. Among them, hsa_circ_0065336 was found to indirectly regulate PTPN11 expression by sponging miR-505-3p. Conclusions These data revealed a comprehensive circRNA-associated ceRNA network during T. asahii infection, thus providing new insights into the pathogenesis of the T. asahii-host interactions. |
Databáze: | OpenAIRE |
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