Borna disease virus infection impacts microRNAs associated with nervous system development, cell differentiation, proliferation and apoptosis in the hippocampi of neonatal rats

Author:                        

Publisher: Spandidos Publications

E-ISSN: 1791-3004|12|3|3697-3703

ISSN: 1791-2997

Source: Molecular Medicine Reports, Vol.12, Iss.3, 2015-01, pp. : 3697-3703

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

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Abstract

MicroRNAs (miRNAs) regulate gene expression by inhibiting transcription or translation and are involved in diverse biological processes, including development, cellular differentiation and tumor generation. miRNA microarray technology is a highthroughput global analysis tool for miRNA expression profiling. Here, the hippocampi of four borna disease virus (BDV)infected and four noninfected control neonatal rats were selected for miRNA microarray and bioinformatic analysis. Reverse transcription quantitative polymerase chain reaction (RTqPCR) analysis was subsequently performed to validate the dysregulated miRNAs. Seven miRNAs (miR145*, miR146a*, miR192*, miR200b, miR223*, miR449a and miR505), showed increased expres­sion, whereas two miRNAs (miR126 and miR374) showed decreased expression in the BDVinfected group. By RTqPCR validation, five miRNAs (miR126, miR200b, miR374, miR449a and miR505) showed significantly decreased expression (P<0.05) in response to BDV infection. Biocarta pathway analysis predicted target genes associated with ‘RNA’, ‘IGF1mTOR’, ‘EIF2’, ‘VEGF’, ‘EIF’, ‘NTHI’, ‘extrinsic’, ‘RB’, ‘IL1R’ and ‘IGF1’ pathways. Gene Ontology analysis predicted target genes associated with ‘peripheral nervous system development’, ‘regulation of small GTPase-mediated signal transduction’, ‘regulation of Ras protein signal transduction’, ‘aerobic respiration’, ‘membrane fusion’, ‘positive regulation of cell cycle’, ‘cellular respiration’, ‘heterocycle metabolic process’, ‘protein tetramerization’ and ‘regulation of Rho protein signal transduction’ processes. Among the five dysregulated miRNAs identified by RTqPCR, miR126, miR200b and miR449a showed a strong association with nervous system development, cell differentiation, proliferation and apoptosis.