Albritton L M, Tseng L, Scadden D, Cunningham J M
Howard Hughes Medical Institute, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.
Cell. 1989 May 19;57(4):659-66. doi: 10.1016/0092-8674(89)90134-7.
Murine type C ecotropic retrovirus infection is initiated by virus envelope binding to a membrane receptor expressed on mouse cells. We have identified a cDNA clone that may encode for this receptor through a strategy combining gene transfer of mouse NIH 3T3 DNA into nonpermissive human EJ cells, selection of EJ clones that have acquired susceptibility to infection by retrovirus vectors containing drug resistance genes, and identification of the putative receptor cDNA clone through linkage to a mouse repetitive DNA sequence. Human EJ cells that express the cDNA acquire a million-fold increase in MuLV infectivity. The predicted 622 amino acid sequence of the putative receptor protein is extremely hydrophobic; 14 potential membrane-spanning domains have been identified. A computer-based search of sequence data banks did not identify a protein with significant similarity to the putative receptor. We conclude that a novel membrane protein determines susceptibility to ecotropic MuLV infection by binding and/or fusion with the virus envelope.
鼠类C型亲嗜性逆转录病毒感染是由病毒包膜与小鼠细胞上表达的膜受体结合引发的。我们通过一种策略鉴定出了一个可能编码该受体的cDNA克隆,该策略包括将小鼠NIH 3T3 DNA基因转移到非允许性人EJ细胞中,筛选出对含有耐药基因的逆转录病毒载体感染获得易感性的EJ克隆,并通过与小鼠重复DNA序列的连锁来鉴定推定的受体cDNA克隆。表达该cDNA的人EJ细胞对MuLV的感染性增加了一百万倍。推定受体蛋白的预测622个氨基酸序列具有极强的疏水性;已鉴定出14个潜在的跨膜结构域。基于计算机对序列数据库的搜索未发现与推定受体具有显著相似性的蛋白质。我们得出结论,一种新型膜蛋白通过与病毒包膜结合和/或融合来决定对亲嗜性MuLV感染的易感性。