Febres V J, Pappu H R, Anderson E J, Pappu S S, Lee R F, Niblett C L
Plant Pathology Department, University of Florida, Gainesville 32611-0680.
Virology. 1994 May 15;201(1):178-81. doi: 10.1006/viro.1994.1282.
Nucleotide sequence analysis of a portion of the citrus tristeza closterovirus (CTV) genome revealed an open reading frame immediately upstream of the coat protein gene that can encode a protein with a calculated M(r) of 27,360 (p27). The deduced amino acid sequence indicated that this putative nonstructural gene product is highly homologous to the coat protein. To investigate whether p27 was expressed in CTV-infected plants, a fusion protein of p27 produced in Escherichia coli was used to raise polyclonal antibodies. Western blot analysis using the p27 antibodies indicated that p27 is expressed in CTV-infected citrus, but not in uninfected plants. Tissue fractionation studies revealed that p27 accumulates in cell wall enriched fractions.
对柑橘衰退病毒(CTV)基因组的一部分进行核苷酸序列分析,结果显示在外壳蛋白基因上游紧邻处有一个开放阅读框,它能够编码一种计算相对分子质量(M(r))为27360的蛋白质(p27)。推导的氨基酸序列表明,这种假定的非结构基因产物与外壳蛋白高度同源。为了研究p27是否在受CTV感染的植物中表达,利用在大肠杆菌中产生的p27融合蛋白制备多克隆抗体。使用p27抗体进行的蛋白质印迹分析表明,p27在受CTV感染的柑橘中表达,但在未感染的植物中不表达。组织分级分离研究显示,p27积累在富含细胞壁的组分中。