Towers G, Bock M, Martin S, Takeuchi Y, Stoye J P, Danos O
Wohl Virion Centre, Windeyer Institute of Medical Sciences, University College London, 46 Cleveland Street, London W1P 6DB, United Kingdom.
Proc Natl Acad Sci U S A. 2000 Oct 24;97(22):12295-9. doi: 10.1073/pnas.200286297.
The murine Fv1 gene restricts infection by N- or B-tropic murine leukemia viruses at a postentry, preintegration stage. The Fv1-sensitive viruses previously used for the study of Fv1 encode an ecotropic envelope gene and thus only infect rodent cells. Consequently, the study of Fv1 restriction has been carried out solely in mice and murine cell lines. By infection with retroviral vectors containing N- or B-tropic core and pantropic vesicular stomatitis virus-G envelope protein, we now demonstrate that cell lines derived from various mammalian species, including humans, have an Fv1-like retrovirus restriction function, preventing N-tropic vector infection. Like Fv1, restriction is directed at amino acid 110 of the viral capsid protein. In contrast to Fv1, the novel restriction is characterized by the absence of reverse-transcribed viral DNA. We speculate that these activities have been selected for by retroviral epidemics in the distant past.
小鼠Fv1基因在病毒进入后、整合前的阶段限制N型或B型嗜性小鼠白血病病毒的感染。先前用于Fv1研究的Fv1敏感病毒编码嗜亲性包膜基因,因此仅感染啮齿动物细胞。因此,Fv1限制作用的研究仅在小鼠和小鼠细胞系中进行。通过感染含有N型或B型嗜性核心以及泛嗜性水泡性口炎病毒G包膜蛋白的逆转录病毒载体,我们现在证明,包括人类在内的各种哺乳动物来源的细胞系具有类似Fv1的逆转录病毒限制功能,可阻止N型嗜性载体感染。与Fv1一样,限制作用针对病毒衣壳蛋白的第110位氨基酸。与Fv1不同的是,这种新的限制作用的特点是不存在逆转录的病毒DNA。我们推测,这些活性在遥远的过去已被逆转录病毒流行所选择。