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Comparison of cDNAs encoding the gibbon ape leukaemia virus receptor from susceptible and non-susceptible murine cells.

Abstract
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.
AuthorsC A Wilson, K B Farrell, M V Eiden
JournalThe Journal of general virology (J Gen Virol) Vol. 75 ( Pt 8) Pg. 1901-8 (Aug 1994) ISSN: 0022-1317 [Print] England
PMID8046392 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Receptors, Virus
  • leukemia virus receptor, gibbon ape
Topics
  • 3T3 Cells
  • Amino Acid Sequence
  • Animals
  • Cloning, Molecular
  • Disease Susceptibility
  • Humans
  • 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

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