Document 0077 DOCN M9490077 TI Comparison of cDNAs encoding the gibbon ape leukaemia virus receptor from susceptible and non-susceptible murine cells. DT 9411 AU Wilson CA; Farrell KB; Eiden MV; Laboratory of Cell Biology, National Institute of Mental Health,; Bethesda, Maryland 20892. SO J Gen Virol. 1994 Aug;75 ( Pt 8):1901-8. Unique Identifier : AIDSLINE MED/94321979 AB The gibbon ape leukaemia virus (GaLV) family of type C retroviruses consists of five closely related viral isolates, GaLV SF, GaLV SEATO, GaLV Br, GaLV H and simian sarcoma-associated virus. The cDNA encoding the human receptor for GaLV SEATO had previously been isolated. We now demonstrate that all of the above GaLVs can use the human form of the GaLV receptor to infect cells. All murine cells analysed to date have been found to be resistant to infection by GaLVs owing to the absence of a functional GaLV receptor. We have now identified a murine cell line which is unique in its susceptibility to GaLV infection. This cell line was established from a Japanese feral mouse, Mus musculus molossinus. We cloned and sequenced the cDNA for the receptor expressed in these cells and compared it to the cDNA for the GaLV receptor expressed in resistant murine cells such as NIH 3T3 (derived from M. m. musculus) and MDTF (derived from M. dunni tail fibroblasts). The crucial region for GaLV infection (the fourth extracellular domain) from the functional M. m. molossinus GaLV receptor is quite divergent from the same region of the M. m. musculus and M. dunni proteins, but similar to that of the functional human GaLV receptor. These results confirm the importance of the amino acids of this region in GaLV receptor function. DE Amino Acid Sequence Animal Cloning, Molecular Comparative Study Disease Susceptibility Human Leukemia Virus, Gibbon Ape/*GROWTH & DEVELOPMENT Leukemia, Experimental/*IMMUNOLOGY Mice Molecular Sequence Data Receptors, Virus/CLASSIFICATION/*GENETICS Retroviridae Infections/*IMMUNOLOGY Sequence Analysis, DNA Sequence Homology, Amino Acid Species Specificity Viral Interference 3T3 Cells JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).