Abstract
A series of replication-competent Moloney murine leukemia virus vectors was constructed in which each vector contained a mutant dihydrofolate reductase (DHFR) cDNA insert in the U3 region of the viral long terminal repeat. Two of the resulting viruses, MLV (murine leukemia virus) DHFR*-5 and MLV DHFR*-7, were able to stably transfer methotrexate resistance to infected fibroblast cells upon multiple rounds of virus replication and in the absence of drug selection. Cell lines producing recombinant virus with high titers were established, which indicated that the insert did not grossly interfere with viral replication functions. These vectors should be useful for introducing and expressing foreign genes in vivo in tissues and whole animals in which virus spread is needed for efficient infection.
MeSH Terms
Animals
Base Sequence
Blotting, Southern
Cloning, Molecular
DNA, Recombinant/biosynthesis
DNA, Viral/biosynthesis
Drug Resistance, Microbial/genetics
Gene Expression Regulation/drug effects
Genetic Vectors
Humans
Methotrexate/pharmacology
Mice
Mice, Inbred Strains
Moloney murine leukemia virus/genetics
Mutation
Nucleic Acid Conformation
Plasmids
Tetrahydrofolate Dehydrogenase/genetics
Transfection
Virus Replication
Chemicals
DNA, Recombinant
DNA, Viral
Tetrahydrofolate Dehydrogenase
Methotrexate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Stuhlmann H
Whitehead Institute for Biomedical Research, Nine Cambridge Center, Massachusetts 02142.
Jaenisch R
Mulligan R C
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