Simón-Mateo C, Andrés G, Almazán F, Viñuela E
Centro de Biología Molecular Severo Ochoa (Consejo Superior de Investigaciones Cientificas-Universidad Autónoma de Madrid), Facultad de Ciencias, Universidad Autonoma de Madrid, Cantoblanco, Spain.
J Virol. 1997 Aug;71(8):5799-804. doi: 10.1128/JVI.71.8.5799-5804.1997.
We have identified an open reading frame (ORF), CP530R, within the EcoRI C' fragment of the African swine fever virus (ASFV) genome that encodes a polyprotein of 62 kDa (pp62). Antisera raised against different regions of ORF CP530R recognized a polypeptide of 62 kDa in ASFV-infected cells during the late phase of virus replication, after the onset of viral DNA synthesis. Pulse-chase experiments showed that polyprotein pp62 is posttranslationally processed to give rise to two proteins of 35 kDa (p35) and 15 kDa (p15). This proteolytic processing was found to take place at the consensus sequence Gly-Gly-X through an ordered cascade of proteolytic cleavages like that which also occurs with ASFV polyprotein pp220 (C. Simón-Mateo, G. Andrés, and E. Viñuela, EMBO J. 12:2977-2987, 1993). Immunofluorescence studies showed that polyprotein pp62 is localized in the viral factories. In addition, immunoprecipitation analysis of purified virus particles showed that mature products p35 and p15 are major structural proteins. According to these results, polyprotein processing represents an essential strategy for the maturation of ASFV structural proteins.
我们在非洲猪瘟病毒(ASFV)基因组的EcoRI C'片段中鉴定出一个开放阅读框(ORF),即CP530R,它编码一种62 kDa的多聚蛋白(pp62)。针对ORF CP530R不同区域产生的抗血清在病毒复制后期、病毒DNA合成开始后,识别出ASFV感染细胞中的一种62 kDa多肽。脉冲追踪实验表明,多聚蛋白pp62在翻译后被加工产生两种蛋白,分别为35 kDa(p35)和15 kDa(p15)。发现这种蛋白水解加工通过像ASFV多聚蛋白pp220那样的有序蛋白水解切割级联反应,在共有序列Gly-Gly-X处发生(C. Simón-Mateo、G. Andrés和E. Viñuela,《欧洲分子生物学组织杂志》12:2977 - 2987,1993年)。免疫荧光研究表明,多聚蛋白pp62定位于病毒工厂。此外,对纯化病毒颗粒的免疫沉淀分析表明,成熟产物p35和p15是主要结构蛋白。根据这些结果,多聚蛋白加工是ASFV结构蛋白成熟的一种基本策略。