van Zeijl M, Johann S V, Closs E, Cunningham J, Eddy R, Shows T B, O'Hara B
Molecular Biology Research Section, American Cyanamid Company, Pearl River, NY 10965.
Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):1168-72. doi: 10.1073/pnas.91.3.1168.
Retrovirus infection is initiated by binding of the viral envelope glycoprotein to a cell-surface receptor. The envelope proteins of type C retroviruses of mammals demonstrate similarities in structural organization and protein sequence. These similarities suggest the possibility that retroviruses from different interference groups might use related proteins as receptors, despite the absence of any relationship between retrovirus receptors isolated to date. To investigate this possibility, we have identified a human cDNA clone encoding a protein closely related to the receptor for gibbon ape leukemia virus and have found that it functions as the receptor for the amphotropic group of murine retroviruses. Expression of this protein (GLVR-2) is likely to be a requirement for infection of human cells by amphotropic retroviral vectors for purposes of gene therapy.
逆转录病毒感染始于病毒包膜糖蛋白与细胞表面受体的结合。哺乳动物C型逆转录病毒的包膜蛋白在结构组织和蛋白质序列上表现出相似性。这些相似性表明,尽管迄今为止分离出的逆转录病毒受体之间没有任何关系,但来自不同干扰组的逆转录病毒可能使用相关蛋白作为受体。为了研究这种可能性,我们鉴定了一个编码与长臂猿白血病病毒受体密切相关的蛋白质的人类cDNA克隆,并发现它作为小鼠逆转录病毒嗜性组的受体发挥作用。这种蛋白质(GLVR-2)的表达可能是嗜性逆转录病毒载体用于基因治疗感染人类细胞的必要条件。