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PMID: 6310140 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Reversal of Fv-1 host range by in vitro restriction endonuclease fragment exchange between molecular clones of N-tropic and B-tropic murine leukemia virus genomes.

Journal of virology ·Vol. 48 ·No. 1 ·1983-10-00 ·Pages 110-9

Boone LR, Myer FE, Yang DM, Ou CY, Koh CK, Roberson LE, Tennant RW, Yang WK

Abstract

We molecularly cloned unintegrated viral DNA of the BALB/c endogenous N-tropic and B-tropic murine leukemia retroviruses and in vitro passaged N-tropic Gross (passage A) murine leukemia retroviruses. Recombinant genomes were constructed in vitro by exchanging homologous restriction enzyme fragments from N- or B-tropic parents and subsequent recloning. Infectious virus was recovered after transfection of these recombinant genomes into NIH-3T3 cells and cocultivation with the Fv-1 nonrestrictive SC-1 cells. XC plaque assays of recombinant virus progeny on Fv-ln and Fv-lb cells indicated that the Fv-l host range was determined by sequences located between the BamHI site in the p30 region of the gag gene (1.6 kilobase pairs from the left end of the map) and the HindIII site located in the pol gene (2.9 kilobase pairs from the left end of the map).

MeSH Terms
AKR murine leukemia virus/genetics,physiology Animals Cell Line Cloning, Molecular DNA Restriction Enzymes DNA, Recombinant Genes, Viral Leukemia Virus, Murine/genetics,physiology Mice Transfection
Chemicals
DNA, Recombinant DNA Restriction Enzymes
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Boone L R
Myer F E
Yang D M
Ou C Y
Koh C K
Roberson L E
Tennant R W
Yang W K
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33 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1983-10-00
Pages
110-9
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC255327
Subset
IM
Grants
NCI NIH HHS · CA 30308 · United States
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