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蚕豆坏死病毒(BBNV)的基因组结构

The genome organization of the broad bean necrosis virus (BBNV).

作者信息

Lu X, Yamamoto S, Tanaka M, Hibi T, Namba S

机构信息

Division of Agricultural and Life Sciences, Graduate School, University of Tokyo, Japan.

出版信息

Arch Virol. 1998;143(7):1335-48. doi: 10.1007/s007050050379.

Abstract

The genome of the broad bean necrosis virus Oita-isolate (BBNV-O) [RNA1 (6.0 kb), RNA2 (2.8 kb) and RNA3 (2.4 kb)] was cloned and sequenced. Computer analysis indicates that methyltransferase, helicase and RNA-dependent RNA polymerase (RdRp) motifs are present in RNA1. The viral capsid protein (CP) cistron is located at the 5' terminal end of RNA2 and the Mr of CP (20 K) is close to that determined by SDS-PAGE analysis. An ochre codon (UAA) in the CP cistron is thought to be partially suppressed to produce a large readthrough protein. RNA3 possesses typical motifs of triple gene block proteins, which are also reported in several other plant viruses. The furovirus genome organization and phylogenetic analysis using RdRp and CP amino acid sequences suggest that BBNV is closely related to potato mop-top virus (PMTV), but is relatively distantly related to other furoviruses. The data also suggest that the genus Furovirus should be separated into several genera: the prototypical genus Furovirus, which excludes the following viruses: the PMTV group including BBNV; the beet necrotic yellow vein virus (BNYVV) group; and the peanut clump virus (PCV) group.

摘要

对蚕豆坏死病毒大分株(BBNV - O)的基因组[RNA1(6.0 kb)、RNA2(2.8 kb)和RNA3(2.4 kb)]进行了克隆和测序。计算机分析表明,RNA1中存在甲基转移酶、解旋酶和RNA依赖的RNA聚合酶(RdRp)基序。病毒衣壳蛋白(CP)顺反子位于RNA2的5'末端,CP的分子量(20 K)与SDS - PAGE分析确定的分子量相近。CP顺反子中的一个赭石密码子(UAA)被认为被部分抑制以产生一个大的通读蛋白。RNA3具有三联基因块蛋白的典型基序,这在其他几种植物病毒中也有报道。使用RdRp和CP氨基酸序列进行的真菌传杆状病毒基因组组织和系统发育分析表明,BBNV与马铃薯帚顶病毒(PMTV)密切相关,但与其他真菌传杆状病毒的关系相对较远。数据还表明,真菌传杆状病毒属应分为几个属:典型的真菌传杆状病毒属,不包括以下病毒:包括BBNV的PMTV组;甜菜坏死黄脉病毒(BNYVV)组;以及花生丛簇病毒(PCV)组。

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