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首页> 外文期刊>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:如在arenavirus双链RNA泛穴中发现的,未配对5'PPP-核苷酸不受钻机的识别

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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:arenavirus和Bunyavirus的RNA基因组是不寻常的,因为它们存在于圆形核衣壳中,可能是由于其互补末端序列的退火。此外,arenavirus基因组合成在模板的位置+2处引发GTP,而不是在精确的3'末端(位置+1)。在形成二核苷酸后,在该引物延长之前,然后在模板上重新调整5'PPPGPCOH。当互补基因组末端退火以形成双链(DsRNA)持续的时,这种“素数和Realign”机制的基因组启动机制的净结果是在不配对的5'核苷酸中发现。使用5'PPPRNA在体外制作并纯化,使得所有DSRNA侧产物不存在,我们已经确定了这两个5'核苷酸突出,以及DSRNA内的不匹配(如在一些arenavirus基因组中),显然降低了这些模型DSRNA在转染到细胞中时诱导干扰素。因此,这种未配对的5'PPP核苷酸的存在是另一种病毒似乎用于避免通过细胞质图案识别受体检测的另一种方式。

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