Suppr超能文献

维多利亚长蠕孢菌190S病毒双链RNA基因组的组织与表达,维多利亚长蠕孢菌190S病毒是一种感染植物病原丝状真菌的全病毒。

Organization and expression of the double-stranded RNA genome of Helminthosporium victoriae 190S virus, a totivirus infecting a plant pathogenic filamentous fungus.

作者信息

Huang S, Ghabrial S A

机构信息

Department of Plant Pathology, University of Kentucky, Lexington 40546-0091, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12541-6. doi: 10.1073/pnas.93.22.12541.

Abstract

The complete nucleotide sequence, 5178 bp, of the totivirus Helminthosporium vicotoriae 190S virus (Hv190SV) double-stranded RNA, was determined. Computer-assisted sequence analysis revealed the presence of two large overlapping ORFs; the 5'-proximal large ORF (ORF1) codes for the coat protein (CP) with a predicted molecular mass of 81 kDa, and the 3'-proximal ORF (ORF2), which is in the -1 frame relative to ORF1, codes for an RNA-dependent RNA polymerase (RDRP). Unlike many other totiviruses, the overlap region between ORF1 and ORF2 lacks known structural information required for translational frameshifting. Using an antiserum to a C-terminal fragment of the RDRP, the product of ORF2 was identified as a minor virion-associated polypeptide of estimated molecular mass of 92 kDa. No CP-RDRP fusion protein with calculated molecular mass of 165 kDa was detected. The predicted start codon of the RDRP ORF (2605-AUG-2607) overlaps with the stop codon (2606-UGA-2608) of the CP ORF, suggesting RDRP is expressed by an internal initiation mechanism. Hv190SV is associated with a debilitating disease of its phytopathogenic fungal host. Knowledge of its genome organization and expression will be valuable for understanding its role in pathogenesis and for potential exploitation in the development of biocontrol measures.

摘要

测定了维多利亚长蠕孢菌190S病毒(Hv190SV)双链RNA的完整核苷酸序列,共5178 bp。计算机辅助序列分析显示存在两个大的重叠开放阅读框;5'近端大开放阅读框(ORF1)编码衣壳蛋白(CP),预测分子量为81 kDa,3'近端开放阅读框(ORF2)相对于ORF1处于-1框架,编码RNA依赖的RNA聚合酶(RDRP)。与许多其他双链RNA病毒不同,ORF1和ORF2之间的重叠区域缺乏翻译移码所需的已知结构信息。使用针对RDRP C末端片段的抗血清,鉴定出ORF2的产物为一种估计分子量为92 kDa的次要病毒粒子相关多肽。未检测到计算分子量为165 kDa的CP-RDRP融合蛋白。RDRP开放阅读框的预测起始密码子(2605-AUG-2607)与CP开放阅读框的终止密码子(2606-UGA-2608)重叠,表明RDRP通过内部起始机制表达。Hv190SV与其植物病原真菌宿主的一种致衰弱疾病有关。了解其基因组组织和表达对于理解其在发病机制中的作用以及在生物防治措施开发中的潜在应用具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5128/38028/21a96ab553e7/pnas01526-0502-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验