Murphy J F, Rychlik W, Rhoads R E, Hunt A G, Shaw J G
Department of Plant Pathology, University of Kentucky, Lexington 40546-0091.
J Virol. 1991 Jan;65(1):511-3. doi: 10.1128/JVI.65.1.511-513.1991.
The identity of the amino acid residue that links the VPg of the potyvirus tobacco vein mottling virus (TVMV) to the viral RNA was determined. 32P-labeled TVMV RNA was digested with RNase A and micrococcal nuclease. The resulting 32P-labeled VPg was isolated and partially hydrolyzed with 6 N HCl at 110 degrees C for 2 h. Analysis by thin-layer electrophoresis revealed the presence of [32P]phosphotyrosine but not [32P]phosphoserine or [32P]phosphothreonine. Another preparation of TVMV RNA was treated with endoproteinase Lys-C, and the resulting peptide-RNA was purified by sodium dodecyl sulfate-sucrose gradient centrifugation. The sequence of the N-terminal 15 amino acid residues of the peptide, when compared with the RNA-derived amino acid sequence of the TVMV polyprotein, demonstrated that the peptide occurs in the small nuclear inclusion protein. These data suggest that Tyr-1860 of the polyprotein is the amino acid residue that links the TVMV VPg to the viral RNA.
确定了将马铃薯Y病毒属烟草脉斑驳病毒(TVMV)的VPg与病毒RNA连接起来的氨基酸残基的身份。用核糖核酸酶A和微球菌核酸酶消化32P标记的TVMV RNA。分离得到的32P标记的VPg,并在110℃下用6N盐酸部分水解2小时。薄层电泳分析显示存在[32P]磷酸酪氨酸,但不存在[32P]磷酸丝氨酸或[32P]磷酸苏氨酸。用内肽酶Lys-C处理另一批TVMV RNA制剂,所得肽-RNA通过十二烷基硫酸钠-蔗糖梯度离心纯化。将该肽N端15个氨基酸残基的序列与TVMV多聚蛋白的RNA衍生氨基酸序列进行比较,结果表明该肽存在于小核内含蛋白中。这些数据表明,多聚蛋白的Tyr-1860是将TVMV VPg与病毒RNA连接起来的氨基酸残基。