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首页> 外文期刊>Journal of biosciences >Down-regulation of human cytomegalovirus UL138, a novel latency-associated determinant, by hcmv-miR-UL36
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Down-regulation of human cytomegalovirus UL138, a novel latency-associated determinant, by hcmv-miR-UL36

机译:hcmv-miR-UL36下调人类巨细胞病毒UL138(一种新的与潜伏期有关的决定因素)

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MicroRNAs (miRNAs) are small RNAs, 19a€“23 nucleotides in length, which regulate a variety of cellular processes. Human cytomegalovirus (HCMV) encodes only one intronic miRNA: human cytomegalovirus microRNA UL36 (hcmv-miR-UL36). In this study, we found that over-expression of hcmv-miR-UL36 resulted in a more than threefold increase in HCMV DNA synthesis at 24 h post infection. Fifteen putative targets of hcmv-miR-UL36 were identified using hybrid PCR, one being the HCMV UL138 gene that has previously been identified as a novel latency-associated determinant of HCMV infection. Down-regulation of UL138 expression by hcmv-miR-UL36 was validated using luciferase reporter assays and Western blot analysis in HEK293 cells. In the presence of hcmv-miR-UL36, we observed a 74.6% decrease in luciferase activity and a 46.2% decrease in HCMV UL138 protein expression. Our results indicate that hcmv-miR-UL36 may be a viral miRNA contributing to HCMV replication.
机译:微小RNA(miRNA)是小的RNA,长度为19a至23个核苷酸,可调节多种细胞过程。人巨细胞病毒(HCMV)仅编码一种内含子miRNA:人巨细胞病毒microRNA UL36(hcmv-miR-UL36)。在这项研究中,我们发现hcmv-miR-UL36的过度表达导致感染后24 h HCMV DNA合成增加了三倍以上。使用混合PCR鉴定了hcmv-miR-UL36的15个推定靶标,其中一个是HCMV UL138基因,该基因先前已被确定为HCMV感染的新型潜伏期相关决定因素。使用萤光素酶报告基因分析和Western印迹分析在HEK293细胞中验证了hcmv-miR-UL36对UL138表达的下调。在hcmv-miR-UL36存在下,我们观察到萤光素酶活性降低了74.6%,HCMV UL138蛋白表达降低了46.2%。我们的结果表明,hcmv-miR-UL36可能是有助于HCMV复制的病毒miRNA。

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