Yugawa T, Amanuma H
Gene Technology and Safety Laboratory, Tsukuba Life Science Center, The Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.
Microbiol Immunol. 1998;42(4):335-9. doi: 10.1111/j.1348-0421.1998.tb02292.x.
Friend spleen focus-forming virus (F-SFFV) is a replication-defective acutely leukemogenic mouse retrovirus and encodes an envelope protein (Env)-like membrane glycoprotein (gp55) in its defective env gene, which is responsible for the early stage of the viral leukemogenesis. Gp55 is a modified Env protein and contains a polytropic mink cell focus-inducing (MCF) murine leukemia virus (MuLV) Env gp70-derived sequence in its amino-terminal region. To evaluate the possibility that the presumed binding of gp55 to an MCF MuLV receptor protein has some role in leukemogenesis, we examined the biological activities of a mutant gp55 (XE gp55), which has a xenotropic MuLV Env gp70 amino-terminal region. XE gp55 displayed almost the same biological activities as the wild-type gp55, excluding the above possibility.
Friend脾集落形成病毒(F-SFFV)是一种复制缺陷型急性致白血病小鼠逆转录病毒,在其缺陷的env基因中编码一种包膜蛋白(Env)样膜糖蛋白(gp55),该蛋白负责病毒白血病发生的早期阶段。Gp55是一种修饰的Env蛋白,在其氨基末端区域含有一个多嗜性水貂细胞集落诱导(MCF)鼠白血病病毒(MuLV)Env gp70衍生序列。为了评估gp55与MCF MuLV受体蛋白的假定结合在白血病发生中是否起作用,我们检测了一种具有嗜异性MuLV Env gp70氨基末端区域的突变型gp55(XE gp55)的生物学活性。XE gp55表现出与野生型gp55几乎相同的生物学活性,排除了上述可能性。