Lei M, Liu Y, Samuel C E
Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara 93106, USA.
Virology. 1998 Jun 5;245(2):188-96. doi: 10.1006/viro.1998.9162.
The virus-associated VAI RNA of adenovirus is a small highly structured RNA that is required for the efficient translation of cellular and viral mRNAs at late times after infection. VAI RNA antagonizes the activation of the interferon-inducible RNA-dependent protein kinase, PKR, an important regulator of translation. The RNA-specific adenosine deaminase, ADAR, is an interferon-inducible RNA-editing enzyme that catalyzes the site-selective C-6 deamination of adenosine to inosine. ADAR possesses three copies of the highly conserved RNA-binding motif (dsRBM) that are similar to the two copies found in PKR, the enzyme in which the prototype dsRBM motif was discovered. We have examined the effect of VAI RNA on ADAR function. VAI RNA impairs the activity of ADAR deaminase. This inhibition can be observed in extracts prepared from interferon-treated human cells and from monkey COS cells in which wild-type recombinant ADAR was expressed. Analysis of wild-type and mutant forms of VA RNA suggests that the central domain is important in the antagonism of ADAR activity. These results suggest that VAI RNA may modulate viral and cellular gene expression by modulating RNA editing as well as mRNA translation.
腺病毒的病毒相关VAI RNA是一种小的高度结构化RNA,在感染后期对于细胞和病毒mRNA的有效翻译是必需的。VAI RNA拮抗干扰素诱导的RNA依赖性蛋白激酶PKR的激活,PKR是翻译的重要调节因子。RNA特异性腺苷脱氨酶ADAR是一种干扰素诱导的RNA编辑酶,它催化腺苷的位点选择性C-6脱氨生成肌苷。ADAR拥有三个高度保守的RNA结合基序(dsRBM)拷贝,这些拷贝与在PKR中发现的两个拷贝相似,PKR是发现原型dsRBM基序的酶。我们研究了VAI RNA对ADAR功能的影响。VAI RNA损害ADAR脱氨酶的活性。在从干扰素处理的人细胞和表达野生型重组ADAR的猴COS细胞制备的提取物中可以观察到这种抑制作用。对野生型和突变型VA RNA的分析表明,中央结构域在拮抗ADAR活性中很重要。这些结果表明,VAI RNA可能通过调节RNA编辑以及mRNA翻译来调节病毒和细胞基因表达。