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花生芽坏死番茄斑萎病毒S RNA:完整核苷酸序列、基因组结构及与其他番茄斑萎病毒的同源性

Peanut bud necrosis tospovirus S RNA: complete nucleotide sequence, genome organization and homology to other tospoviruses.

作者信息

Satyanarayana T, Mitchell S E, Reddy D V, Brown S, Kresovich S, Jarret R, Naidu R A, Demski J W

机构信息

Crop Protection Division, International Crops Research Institute for the Semi-Arid Tropics Asia Center (ICRISAT-IAC), Patancheru, India.

出版信息

Arch Virol. 1996;141(1):85-98. doi: 10.1007/BF01718590.

Abstract

The complete nucleotide sequence of the S RNA of peanut bud necrosis virus (PBNV) has been determined. The RNA is 3 057 nucleotides in length, contains inverted repeats and two open reading frames (ORFs) with an ambisense coding strategy that are separated by an A+U-rich intergenic region. One ORF (1 320 nucleotides in the viral sense strand) encodes a Mr 49.5 kDa protein, identified as the nonstructural (NSs) protein based on similarity to published tospovirus sequences. The second ORF (831 nucleotides in virus complementary strand) encodes a Mr 30.6 kDa protein. This protein was identified as the nucleocapsid (N) protein based on sequence similarities. Amino acid sequence comparison of N and NSs proteins revealed identities of 22-34% with the reported tospovirus isolates of serogroups I, II, and III, whereas it had 82-86% identity with viruses in serogroup IV, watermelon silver mottle virus (WSMV) and tomato isolate of peanut bud necrosis (PBNV-To). Two subgenomic RNA species detected in PBNV infected tissue corresponded to the predicted sizes (1.65 and 1.4 kb) of the NSs and N mRNAs. The data presented show conclusively that PBNV should be included in serogroup IV, along with WSMV and PBNV-To.

摘要

花生芽坏死病毒(PBNV)S RNA的完整核苷酸序列已被测定。该RNA长度为3057个核苷酸,含有反向重复序列以及两个开放阅读框(ORF),采用双义编码策略,二者被富含A+U的基因间隔区隔开。一个ORF(病毒正义链上1320个核苷酸)编码一种49.5 kDa的蛋白质,基于与已发表的番茄斑萎病毒序列的相似性,该蛋白质被鉴定为非结构(NSs)蛋白。第二个ORF(病毒互补链上831个核苷酸)编码一种30.6 kDa的蛋白质。基于序列相似性,该蛋白质被鉴定为核衣壳(N)蛋白。N蛋白和NSs蛋白的氨基酸序列比较显示,与血清群I、II和III中已报道的番茄斑萎病毒分离株的同一性为22%-34%,而与血清群IV中的病毒、西瓜银斑驳病毒(WSMV)和花生芽坏死病毒番茄分离株(PBNV-To)的同一性为82%-86%。在PBNV感染组织中检测到的两种亚基因组RNA种类与NSs和N mRNA的预测大小(1.65和1.4 kb)相对应。所呈现的数据确凿地表明,PBNV应与WSMV和PBNV-To一起归入血清群IV。

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