Marq Jean-Baptiste, Kolakofsky Daniel, Garcin Dominique
Department of Microbiology and Molecular Medicine, University of Geneva School of Medicine, CMU, 9 Avenue de Champel, 1211 Geneva, Switzerland.
J Biol Chem. 2010 Jun 11;285(24):18208-16. doi: 10.1074/jbc.M109.089425. Epub 2010 Apr 16.
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' pppGpC(OH) 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.
沙粒病毒和布尼亚病毒的RNA基因组不同寻常,因为它们存在于环状核衣壳中,推测这是由于其互补末端序列退火的缘故。此外,沙粒病毒基因组合成起始于模板上第+2位的鸟苷三磷酸(GTP),而非精确的3'末端(第+1位)。形成二核苷酸后,5' pppGpC(OH)在该引物延伸之前先在模板上重新排列。这种基因组起始的“引物和重新排列”机制的最终结果是,当互补基因组末端退火形成双链(dsRNA)柄状结构时,5' pppG作为未配对的5'核苷酸存在。使用体外制备并纯化以去除所有双链RNA副产物的5' pppRNA,我们已经确定,这种5'核苷酸突出端以及双链RNA内的错配(如在一些沙粒病毒基因组中发现的),在转染到细胞中时都会明显降低这些模型双链RNA诱导干扰素的能力。因此,这种未配对的5' ppp -核苷酸的存在是一些病毒似乎用来逃避细胞质模式识别受体检测的另一种方式。