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首页> 外文期刊>Genetics and Molecular Research >'Drosha, DGCR8, and Dicer mRNAs are downregulated in human cells infected with dengue virus 4' - Genet. Mol. Res. 15 (2): gmr.15027891 - Drosha, Dicer, and TRBP mRNA are downregulated in Vero cells with the 3'UTR of Dengue virus
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'Drosha, DGCR8, and Dicer mRNAs are downregulated in human cells infected with dengue virus 4' - Genet. Mol. Res. 15 (2): gmr.15027891 - Drosha, Dicer, and TRBP mRNA are downregulated in Vero cells with the 3'UTR of Dengue virus

机译:“ Drosha,DGCR8和Dicer mRNA在受登革热病毒4感染的人类细胞中被下调”-Genet。大声笑Res。 15(2):gmr.15027891-登革热病毒3'UTR在Vero细胞中下调了Drosha,Dicer和TRBP mRNA

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Dear Editor,A recent paper (Casseb et al., 2016) published in the journal Genetics and Molecular Research described the interesting concept that dengue virus (DENV)-4 infection, in the human cell line A-549, leads to the downregulation of expression of key components of microRNA (miRNA) biogenesis, such as Drosha, Dicer, and DGCR8. For this, the authors performed a time course infection of A-549 cells for 5 days. The highest viral load was observed at 3 days post-infection, which corresponded with the maximum downregulation of expression of Drosha, Dicer, and DGCR8, assayed by quantitative PCR (RT-qPCR). These results supported the recent notion of a complex interaction between DENV and the host miRNA machinery and of the host miRNA response to this particular infection. Extensive evidence has shown that DENV can take advantage of host miRNAs for its own replication (Zhu et al., 2014) and that host miRNAs can inhibit DENV replication (Wu et al., 2013).
机译:亲爱的编辑,最近发表在《遗传与分子研究》杂志上的一篇论文(Casseb等人,2016年)描述了一个有趣的概念,即人类细胞系A-549中的登革热病毒(DENV)-4感染会导致其下调。 microRNA(miRNA)生物发生关键成分的表达,例如Drosha,Dicer和DGCR8。为此,作者进行了A-549细胞的时程感染5天。感染后3天观察到最高的病毒载量,这与通过定量PCR(RT-qPCR)分析的Drosha,Dicer和DGCR8表达的最大下调相对应。这些结果支持了DENV与宿主miRNA机制之间复杂的相互作用以及宿主对这种特定感染的miRNA反应的最新观点。大量证据表明,DENV可以利用宿主miRNA进行自身复制(Zhu等人,2014),并且宿主miRNA可以抑制DENV复制(Wu等人,2013)。

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