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PMID: 2927389 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Construction and properties of replication-competent murine retroviral vectors encoding methotrexate resistance.

Molecular and cellular biology ·Vol. 9 ·No. 1 ·1989-01-00 ·Pages 100-8

Stuhlmann H, Jaenisch R, Mulligan RC

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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26 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1989-01-00
Pages
100-8
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC362150
Subset
IM
Grants
NCI NIH HHS · CA38497 · United States
NICHD NIH HHS · HD00635 · United States
NHLBI NIH HHS · HL37569 · United States
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