Johann S V, van Zeijl M, Cekleniak J, O'Hara B
Molecular Biology Research Section, Lederle Laboratories, American Cyanamid Company, Pearl River, New York 10965.
J Virol. 1993 Nov;67(11):6733-6. doi: 10.1128/JVI.67.11.6733-6736.1993.
Expression of human GLVR1 in mouse cells confers susceptibility to infection by gibbon ape leukemia virus (GALV), while the normally expressed mouse Glvr-1 does not. Since human and murine GLVR1 proteins differ at 64 positions in their sequences, some of the residues differing between the two proteins are critical for infection. To identify these, a series of hybrids and in vitro-constructed mutants were tested for the ability to confer susceptibility to infection. The results indicated that human GLVR1 residues 550 to 551, located in a cluster of seven of the sites that differ between the human and mouse proteins, are the only residues differing between the two which must be in the human protein form to allow infection. Sequencing of a portion of GLVR1 from the rat (which is infectible) confirmed the importance of this cluster in that it contained the only notable differences between the rat and mouse proteins. This region, which also differs substantially between the rat and the human proteins, therefore exhibits a pronounced tendency for polymorphism.
人类GLVR1在小鼠细胞中的表达使细胞对长臂猿白血病病毒(GALV)感染敏感,而正常表达的小鼠Glvr-1则不然。由于人类和小鼠的GLVR1蛋白在序列上有64个位置不同,这两种蛋白之间不同的一些残基对感染至关重要。为了确定这些残基,对一系列杂交体和体外构建的突变体进行了感染敏感性赋予能力的测试。结果表明,人类GLVR1的550至551位残基位于人类和小鼠蛋白不同的七个位点簇中,是两种蛋白之间不同的唯一残基,必须是人类蛋白形式才能允许感染。对来自大鼠(可感染)的部分GLVR1进行测序证实了该簇的重要性,因为它包含大鼠和小鼠蛋白之间唯一显著的差异。该区域在大鼠和人类蛋白之间也有很大差异,因此表现出明显的多态性倾向。