In vitro synthesis of infectious retroviral RNA

Author:

Flamant F1,Sorge J A1

Affiliation:

1. Department of Basic and Clinical Research, Research Institute of Scripps Clinic, La Jolla, California 92037.

Abstract

A plasmid was constructed in which a T7 RNA polymerase promoter was placed upstream of a recombinant amphotropic retrovirus genome containing a selectable neomycin resistance gene. To test the infectivity of the RNA produced by T7 RNA polymerase in vitro, the RNA was microinjected into the nuclei of psi 2 packaging cells. Infectious particles conferring G418 resistance were released.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference13 articles.

1. New RNA polymerase from E. coli infected with bacteriophage T7;Chamberlin M.;Nature (London),1970

2. High-frequency deletion in recovered retrovirus vectors containing exogenous DNA with promoters;Emerman M.;J. Virol.,1984

3. Activation of cellular onc gene by promoter insertion in ALV induced lymphoid leukosis;Hayward H. S.;Nature (London),1981

4. Precise localization of m6A in Rous sarcoma virus RNA reveals clustering of methylation sites: implication for RNA processing;Kane S. E.;Mol. Cell. Biol.,1985

5. Expression of a foreign gene in myeloid and Iymphoid progency of common hemopoietic precursors;Keller G.;Nature (London),1985

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