首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Unpaired 5′ ppp-Nucleotides as Found in Arenavirus Double-stranded RNA Panhandles Are Not Recognized by RIG-I
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Unpaired 5′ ppp-Nucleotides as Found in Arenavirus Double-stranded RNA Panhandles Are Not Recognized by RIG-I

机译:RIG-I无法识别在无粒病毒双链RNA泛柄中发现的未配对的5ppp核苷酸。

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摘要

Arenavirus and bunyavirus RNA genomes are unusual in that they are found in circular nucleocapsids, presumably due to the annealing of their complementary terminal sequences. Moreover, arenavirus genome synthesis initiates with GTP at position +2 of the template rather than at the precise 3′ end (position +1). After formation of a dinucleotide, 5′ pppGpCOH is then realigned on the template before this primer is extended. The net result of this “prime and realign” mechanism of genome initiation is that 5′ pppG is found as an unpaired 5′ nucleotide when the complementary genome ends anneal to form a double-stranded (dsRNA) panhandle. Using 5′ pppRNA made in vitro and purified so that all dsRNA side products are absent, we have determined that both this 5′ nucleotide overhang, as well as mismatches within the dsRNA (as found in some arenavirus genomes), clearly reduce the ability of these model dsRNAs to induce interferon upon transfection into cells. The presence of this unpaired 5′ ppp-nucleotide is thus another way that some viruses appear to use to avoid detection by cytoplasmic pattern recognition receptors.
机译:腔病毒和布尼亚病毒RNA基因组之所以与众不同,是因为它们在环状核衣壳中发现,大概是由于它们互补末端序列的退火所致。此外,砂粒病毒基因组的合成起始于模板的+2位置而不是精确的3'端(+1位置)的GTP。在形成二核苷酸后,在延伸该引物之前,将5'pppGpCOH在模板上重新比对。基因组启动的这种“启动和重新排列”机制的最终结果是,当互补基因组结束退火以形成双链(dsRNA)泛柄时,发现5'pppG为未配对的5'核苷酸。使用体外制备和纯化的5'pppRNA,使所有dsRNA副产物均不存在,我们已确定,这5'核苷酸突出端以及dsRNA内的错配(如在某些arenavirus基因组中发现的)明显降低了这些模型dsRNA在转染入细胞后诱导干扰素。因此,这种未配对的5'ppp核苷酸的存在是某些病毒似乎用来避免被细胞质模式识别受体检测的另一种方式。

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