Moreau-Gachelin F, Robert-Lezenes J, Mathieu-Mahul D, Gisselbrecht S, Larsen C J
Biochimie. 1983 Apr-May;65(4-5):259-66. doi: 10.1016/s0300-9084(83)80277-6.
Viral expression was analyzed in ten cell clones of a Friend erythroleukemia cell line (HFL/b cell line [3]), which had lost its capacity to produce infectious particles. All the ten subclones were non producers but expressed spleen focus forming virus (SFFV) polypeptides in the form of p48-p50gag and gp50-gp52env. One subclone (subclone 9) expressed the gp70env of the Friend-MuLV helper component of the Friend virus complex. Comparative analysis of viral RNA expression in one gp70- subclone (subclone 2) and in the gp70+ subclone (subclone 9) was performed using specific ecotropic env gene probe and MCF/xenotropic env gene probe. In both subclones 2 and 9, the MCF/xenotropic env gene probe detected 32S SFFV genomic RNA, 20S SFFV env gene mRNA and a 34S RNA. The ecotropic env probe failed to characterize any 38S F-MuLV genomic RNA in both clones but detected 34S RNA and 24S env mRNA in the gp70+ subclone 9. These data show that expression of a complete F-MuLV genome is not required for synthesis of env gene products.
在一种已丧失产生感染性颗粒能力的弗氏红白血病细胞系(HFL/b细胞系[3])的十个细胞克隆中分析了病毒表达情况。所有这十个亚克隆均不产生病毒,但以p48 - p50gag和gp50 - gp52env的形式表达脾集落形成病毒(SFFV)多肽。一个亚克隆(亚克隆9)表达了弗氏病毒复合体的弗氏 - MuLV辅助成分的gp70env。使用特异性嗜亲性env基因探针和MCF/异嗜性env基因探针,对一个gp70 - 亚克隆(亚克隆2)和gp70 + 亚克隆(亚克隆9)中的病毒RNA表达进行了比较分析。在亚克隆2和9中,MCF/异嗜性env基因探针均检测到32S SFFV基因组RNA、20S SFFV env基因mRNA和一种34S RNA。嗜亲性env探针未能在两个克隆中鉴定出任何38S F - MuLV基因组RNA,但在gp70 + 亚克隆9中检测到34S RNA和24S env mRNA。这些数据表明,env基因产物的合成不需要完整的F - MuLV基因组的表达。