Pinter A, Honnen W J
Virology. 1985 Jun;143(2):646-50. doi: 10.1016/0042-6822(85)90406-4.
The env genes of Friend spleen focus-forming viruses (F-SFFV) have been implicated in the rapid pathogenicity of these agents. Two env-gene products are detected in SFFV-infected cells: the primary translation product, gp52, and a more highly processed form, gp65. In this communication we demonstrate that gp65 is the major end product of the SFFV env gene, and is efficiently secreted from both erythroleukemia cells and infected fibroblasts. Secretion was observed for the mature env-gene products of both polycythemia- and anemia-inducing strains of SFFV. These results suggest that one function of the point mutation near the 3' end of the env gene, which is invariant in the formation of SFFVs, is to allow secretion of gp65, and that secreted gp65 may be the factor mediating the leukemogenic activity of these viruses.
弗瑞德脾脏灶形成病毒(F-SFFV)的env基因与这些病原体的快速致病性有关。在感染SFFV的细胞中可检测到两种env基因产物:初级翻译产物gp52和一种加工程度更高的形式gp65。在本通讯中,我们证明gp65是SFFV env基因的主要终产物,并能从红白血病细胞和受感染的成纤维细胞中有效分泌。在诱导红细胞增多症和贫血的SFFV毒株的成熟env基因产物中均观察到了分泌现象。这些结果表明,env基因3'端附近的点突变在SFFV形成过程中是不变的,其功能之一是允许gp65分泌,并且分泌的gp65可能是介导这些病毒致白血病活性的因子。