Abstract
A recombinant murine retrovirus was constructed which contains, within its genome, a truncated version of the gene encoding the murine H-2L(d) major histocompatibility antigen. The H-2L(d) gene, which was inserted 3' of the env splice acceptor site in the recombinant retrovirus MSV-neo, lacked the 5' promoter and TATA sequences and the 3' transcription termination and polyadenylate addition sites of the normal H-2L(d) gene. Transfection of the MSV-neo/H-2L(d) plasmid (pLTV-11) into Y-2 cells resulted in the production of the transmissible recombinant retrovirus LTV-11. Cells infected with LTV-11 virus were resistant to the eucaryotic antibiotic G418 and expressed H-2L(d) on the cell surface. These infected cells contained a viral RNA species which possessed both the H-2L(d) and the neomycin resistance gene sequences but did not contain significant levels of the smaller H-2L(d)-specific mRNA. The H-2L(d) antigen expressed on the surface of infected cells functioned as a target for cytolytic T cells specific for the H-2L(d) antigen.
Original language | English (US) |
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Pages (from-to) | 1379-1384 |
Number of pages | 6 |
Journal | Molecular and cellular biology |
Volume | 5 |
Issue number | 6 |
DOIs | |
State | Published - 1985 |
ASJC Scopus subject areas
- Molecular Biology
- Cell Biology