Whiteley S A, Naso R B
J Virol. 1981 Mar;37(3):860-70. doi: 10.1128/JVI.37.3.860-870.1981.
Intracellular precursor polyproteins of three baboon endogenous retrovirus (BaEV) isolates, m7, 455K, and BILN, were compared with the intracellular proteins of the type C human isolated HL23V by radioimmunoprecipitation, followed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and tryptic peptide analysis. Human and canine cells infected with m7-BaEV and canine thymus cells infected with BILN-BaEV were characterized by identical precursor polyproteins Pr85gag, Pr70-71gag, Pr65gag, and gPr85env. Canine cells infected with 455K-BaEV consistently showed a slightly different pattern of precursor polyproteins. These included Pr85gag, Pr70gag, Pr67gag, and gPR85env. By tryptic digest mapping of peptides containing [3H]leucine, m7-BaEV and 455K-BaEV were shown to be highly related. By comparison, mapping studies showed that BILN-BaEV was less highly related to m7-BaEV than ws 455K-BaEV. Differences in these related BaEV isolates presumably reflected virus-specific differential cleavage of core protein precursors or alterations in polyprotein primary structure or both. Chase-incubated cells infected with BaEV also contained a stable, p28-related polyprotein termed P72gag. This polyprotein migrated upon sodium dodecyl sulfate-polyacrylamide gel electrophoresis slightly slower than the major core protein precursor Pr70-71gag and appeared to arise by posttranslational modification of Pr70-71gag. Immunoprecipitation of extracts of HL23V-infected cells with antisera to simian sarcoma-simian-associated virus proteins and BaEV proteins confirmed that these cells contained two unrelated viral components, one that was similar to m7-BaEV or BILN-BaEV and a second that was related to simian sarcoma-simian-associated virus. Tryptic digest mapping of BaEV and HL23V prcursor polyproteins suggested that the BaEV-like component of HL23V weas more closely related to m7-BaEV than to 455K-BaEV or BILN-BaEV.
通过放射免疫沉淀,随后进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和胰蛋白酶肽分析,比较了三种狒狒内源性逆转录病毒(BaEV)分离株m7、455K和BILN的细胞内前体多聚蛋白与C型人类分离株HL23V的细胞内蛋白。感染m7-BaEV的人和犬细胞以及感染BILN-BaEV的犬胸腺细胞的特征是具有相同的前体多聚蛋白Pr85gag、Pr70 - 71gag、Pr65gag和gPr85env。感染455K-BaEV的犬细胞始终显示出略有不同的前体多聚蛋白模式。这些包括Pr85gag、Pr70gag、Pr67gag和gPR85env。通过对含[³H]亮氨酸的肽进行胰蛋白酶消化图谱分析,显示m7-BaEV和455K-BaEV高度相关。相比之下,图谱研究表明BILN-BaEV与m7-BaEV的相关性不如与455K-BaEV的相关性高。这些相关的BaEV分离株之间的差异可能反映了核心蛋白前体的病毒特异性差异切割或多聚蛋白一级结构的改变或两者皆有。用BaEV感染并进行追踪培养的细胞还含有一种稳定的、与p28相关的多聚蛋白,称为P72gag。这种多聚蛋白在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上的迁移速度比主要核心蛋白前体Pr70 - 71gag略慢,似乎是由Pr70 - 71gag的翻译后修饰产生的。用抗猿猴肉瘤-猿猴相关病毒蛋白和BaEV蛋白的抗血清对HL23V感染细胞的提取物进行免疫沉淀,证实这些细胞含有两种不相关的病毒成分,一种与m7-BaEV或BILN-BaEV相似,另一种与猿猴肉瘤-猿猴相关病毒有关。对BaEV和HL23V前体多聚蛋白的胰蛋白酶消化图谱分析表明,HL23V中类似BaEV的成分与m7-BaEV的关系比与455K-BaEV或BILN-BaEV的关系更密切。