Filichkin S A, Lister R M, McGrath P F, Young M J
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.
Virology. 1994 Nov 15;205(1):290-9. doi: 10.1006/viro.1994.1645.
The barley yellow dwarf virus (BYDV) coat protein gene is separated from an adjacent downstream open reading frame (ORF) by a single termination codon. Immunological analysis of this downstream "readthrough" region reveals multiple coat protein-readthrough products. A full-length 72-kDa (P72) coat protein-readthrough fusion product is detected in total lysates from infected cells. However, purified aphid transmissible virions contain only a 50-kDa (P50) coat protein-readthrough product. Virion-associated P50 lacks the C-terminal domain predicted by its ORF sequence. A separate 33-kDa polypeptide (P33) corresponding to the readthrough C-terminus domain is detected in the crude cellular membrane fraction. Site-directed and deletion mutational analysis demonstrate that the readthrough ORF is dispensable for BYDV replication and virion accumulation in protoplasts. In contrast, a mutant which results in a continuous fusion product of coat and readthrough sequences is not viable. Point mutations were used to map regions required for P50 and P72 synthesis. A model explaining the relationships between the three forms of the readthrough polypeptides is proposed.
大麦黄矮病毒(BYDV)外壳蛋白基因与相邻的下游开放阅读框(ORF)之间由一个终止密码子隔开。对该下游“通读”区域的免疫学分析揭示了多种外壳蛋白通读产物。在感染细胞的总裂解物中检测到全长72 kDa(P72)的外壳蛋白通读融合产物。然而,纯化的蚜虫可传播病毒粒子仅含有50 kDa(P50)的外壳蛋白通读产物。与病毒粒子相关的P50缺少其ORF序列预测的C末端结构域。在粗制细胞膜组分中检测到一种与通读C末端结构域相对应的单独的33 kDa多肽(P33)。定点和缺失突变分析表明,通读ORF对于BYDV在原生质体中的复制和病毒粒子积累并非必需。相反,产生外壳蛋白和通读序列连续融合产物的突变体无法存活。点突变用于定位P50和P72合成所需的区域。提出了一个解释通读多肽三种形式之间关系的模型。