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甲型流感病毒可诱导抗逆转录病毒蛋白载脂蛋白B mRNA编辑酶催化多肽样蛋白3G(APOBEC3G)的高水平表达,但该蛋白不具有抗病毒活性。

High level expression of the anti-retroviral protein APOBEC3G is induced by influenza A virus but does not confer antiviral activity.

作者信息

Pauli Eva-K, Schmolke Mirco, Hofmann Henning, Ehrhardt Christina, Flory Egbert, Münk Carsten, Ludwig Stephan

机构信息

Institute of Molecular Virology, Centre of Molecular Biology of Inflammation (ZMBE), Westfaelische-Wilhelms-University Muenster, Münster, Germany.

出版信息

Retrovirology. 2009 Apr 16;6:38. doi: 10.1186/1742-4690-6-38.

Abstract

Human APOBEC3G is an antiretroviral protein that was described to act via deamination of retroviral cDNA. However, it was suggested that APOBEC proteins might act with antiviral activity by yet other mechanisms and may also possess RNA deamination activity. As a consequence there is an ongoing debate whether APOBEC proteins might also act with antiviral activity on other RNA viruses. Influenza A viruses are single-stranded RNA viruses, capable of inducing a variety of antiviral gene products. In searching for novel antiviral genes against these pathogens, we detected a strong induction of APOBEC3G but not APOBEC3F gene transcription in infected cells. This upregulation appeared to be induced by the accumulation of viral RNA species within the infected cell and occurred in an NF-kappaB dependent, but MAP kinase independent manner. It further turned out that APOBEC expression is part of a general IFNbeta response to infection. However, although strongly induced, APOBEC3G does not negatively affect influenza A virus propagation.

摘要

人类载脂蛋白B mRNA编辑酶催化多肽样蛋白3G(APOBEC3G)是一种抗逆转录病毒蛋白,其作用机制是对逆转录病毒cDNA进行脱氨基作用。然而,有研究表明,载脂蛋白B mRNA编辑酶催化多肽样蛋白(APOBEC)家族蛋白可能通过其他机制发挥抗病毒活性,并且可能还具有RNA脱氨基活性。因此,关于APOBEC家族蛋白是否也能对其他RNA病毒发挥抗病毒活性,目前仍存在争议。甲型流感病毒是单链RNA病毒,能够诱导多种抗病毒基因产物的产生。在寻找针对这些病原体的新型抗病毒基因时,我们发现受感染细胞中APOBEC3G基因转录被强烈诱导,但APOBEC3F基因转录未被诱导。这种上调似乎是由受感染细胞内病毒RNA种类的积累所诱导的,并且以一种依赖核因子κB(NF-κB)但不依赖丝裂原活化蛋白激酶(MAP激酶)的方式发生。进一步研究发现,APOBEC表达是对感染的一般干扰素β(IFNβ)反应的一部分。然而,尽管APOBEC3G被强烈诱导,但它并不会对甲型流感病毒的增殖产生负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc20/2672920/deaaf5010bd2/1742-4690-6-38-1.jpg

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