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爱泼斯坦-巴尔病毒介导的人类微小RNA表达失调

Epstein-Barr virus-mediated dysregulation of human microRNA expression.

作者信息

Godshalk Sirie E, Bhaduri-McIntosh Sumita, Slack Frank J

机构信息

Yale University, Department of Molecular, Cellular and Developmental Biology, New Haven, Connecticut 06520, USA.

出版信息

Cell Cycle. 2008 Nov 15;7(22):3595-600. doi: 10.4161/cc.7.22.7120. Epub 2008 Nov 2.

Abstract

MicroRNAs (miRNAs) are a large class of small (approximately 22 nt) noncoding RNAs that negatively regulate gene expression most often at the level of translation, and have been shown to be key regulators in a variety of processes including development, cell cycle and immunity. The Epstein-Barr virus (EBV) is an oncogenic herpes virus endemic in humans that encodes at least twenty-two of its own miRNAs. Cellular miRNAs have well-established roles in cancer and immune pathways, and multiple cellular miRNAs directly target viral messages. Additionally, multiple viruses express suppressors of cellular RNAi-induced silencing. Here we show that EBV de novo infection of primary cultured human B-cells results in a dramatic downregulation of cellular miRNA expression, suggesting the virus may encode or activate a suppressor of miRNA expression. We additionally show that the immuno-modulatory microRNA miR-146a, downregulated on initial infection, is significantly upregulated more than 100-fold upon induction of the viral lytic cycle, and appears to have inhibitory effects on the progression of the lytic cycle. Our results show that EBV has substantial effects on cellular miRNA expression.

摘要

微小RNA(miRNA)是一大类小的(约22个核苷酸)非编码RNA,其最常通过翻译水平对基因表达进行负调控,并且已被证明是包括发育、细胞周期和免疫在内的多种过程中的关键调节因子。爱泼斯坦-巴尔病毒(EBV)是一种在人类中流行的致癌性疱疹病毒,其自身编码至少22种miRNA。细胞miRNA在癌症和免疫途径中具有明确的作用,并且多种细胞miRNA直接靶向病毒信息。此外,多种病毒表达细胞RNAi诱导沉默的抑制因子。在此我们表明,EBV对原代培养的人B细胞的从头感染导致细胞miRNA表达显著下调,这表明该病毒可能编码或激活一种miRNA表达抑制因子。我们还表明,免疫调节性miRNA miR-146a在初次感染时下调,在病毒裂解周期诱导后显著上调超过100倍,并且似乎对裂解周期的进展具有抑制作用。我们的结果表明,EBV对细胞miRNA表达有实质性影响。

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