首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Characterization of Wuhan Nodavirus subgenomic RNA3 and the RNAi inhibition property of its encoded protein B2.
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Characterization of Wuhan Nodavirus subgenomic RNA3 and the RNAi inhibition property of its encoded protein B2.

机译:武汉诺达病毒亚基因组RNA3的表征及其编码蛋白B2的RNAi抑制特性。

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摘要

Wuhan Nodavirus (WhNV) is the first reported nodavirus isolated from insect in China. The viral genome consists of two positive-strand RNA, RNA1 and RNA2. RNA1 is 3149 nucleotides in length, and contains three putative Open Reading Frames (ORFs) which encode proteins A, B1 and B2, respectively. In contrast, only one putative ORF encoding protein alpha was identified within 1562-nt-long RNA2 species. Here, we report the newly characterized molecular properties of WhNV subgenomic RNA3 and its encoded protein B2. We have successfully multiplied WhNV in the natural host Pieris rapae larvae under laboratory conditions. WhNV replication in the host cells resulted in the expression of viral proteins, ProA, B2 and Proalpha, with the absence of B1 production. Northern blot hybridization assay revealed the existence of subgenomic RNA3 which is 5' capped and 3' co-terminal with RNA1. The subgenomic RNA3 is 370 nucleotides in length and contains only one ORF (B2) with the first AUG as the authentic initiation codon. In addition, we found that nonstructural protein B2 of WhNV is an efficient RNA interference (RNAi) suppressor in a cultured drosophila cell line. The amino-terminal region (aa 1-20) of B2 is essential for this RNAi inhibition activity.
机译:武汉诺达病毒(WhNV)是中国第一个从昆虫中分离出的诺达病毒。病毒基因组由两个正链RNA RNA1和RNA2组成。 RNA1的长度为3149个核苷酸,并包含三个假定的开放阅读框(ORF),分别编码蛋白质A,B1和B2。相反,在1562个核苷酸长的RNA2物种中仅鉴定出一个推定的ORF编码蛋白α。在这里,我们报告WhNV亚基因组RNA3及其编码的蛋白质B2的新表征的分子特性。我们已经在实验室条件下成功地在天然寄主菜青虫幼虫中繁殖了WhNV。 WhNV在宿主细胞中的复制导致病毒蛋白ProA,B2和Proalpha的表达,而没有B1的产生。 Northern印迹杂交测定法揭示了亚基因组RNA3的存在,该亚基因组RNA3被5'加帽并且与RNA1共末端。亚基因组RNA3的长度为370个核苷酸,仅包含一个ORF(B2),且第一个AUG为真实的起始密码子。此外,我们发现WhNV的非结构蛋白B2在果蝇培养的细胞系中是一种有效的RNA干扰(RNAi)抑制剂。 B2的氨基末端区域(aa 1-20)对于这种RNAi抑制活性至关重要。

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