Abstract |
The relationship between the putative bovine leukemia virus receptor gene (BVLRcp) and the susceptibility of human cells to BLV infection was studied. Three cDNA clones encoding different portions of the human equivalent of bovine BLVRcp1 were isolated by DNA- DNA hybridization by comparison of the human cDNA clones to bovine BLVRcp1. Amino acid sequence indicated that the human sequence encodes the delta subunit of the AP-3 adaptor-related protein. When the recombinant human homologue BLVRcp2 was expressed in E. coli, it failed to bind the BLVgp51. However, the BVLVgp51 binding ability was restored when the chimerical BLVRcp molecule was prepared by exchanging 5' ends between bovine and human BLVRcp cDNAs. This finding implies that this BLVgp51 binding site is present only on the bovine BLVRcp and therefore its human homologue cannot be recognized by BLVgp51. This might also explain the resistance of human cells to BLV infection.
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Authors | J Ban, J Hlavaty, O Orlik, G A Splitter, C Altaner |
Journal | Archives of virology
(Arch Virol)
Vol. 144
Issue 10
Pg. 2013-22
( 1999)
ISSN: 0304-8608 [Print] Austria |
PMID | 10550673
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- AP3D1 protein, human
- Adaptor Protein Complex 3
- Adaptor Protein Complex delta Subunits
- BLVR protein, Bos taurus
- DNA, Complementary
- Membrane Proteins
- Receptors, Virus
- Recombinant Fusion Proteins
- Transcription Factors
- Viral Envelope Proteins
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Topics |
- Adaptor Protein Complex 3
- Adaptor Protein Complex delta Subunits
- Animals
- Blotting, Southern
- Blotting, Western
- Cattle
- DNA, Complementary
(genetics)
- Humans
- Leukemia Virus, Bovine
(metabolism, pathogenicity)
- Male
- Membrane Proteins
- Receptors, Virus
(genetics, metabolism)
- Recombinant Fusion Proteins
(metabolism)
- Sequence Homology, Amino Acid
- Species Specificity
- Transcription Factors
(genetics, metabolism)
- Tumor Cells, Cultured
- Viral Envelope Proteins
(genetics, metabolism)
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