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PMID: 6229454 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning of Herpesvirus saimiri DNA fragments representing the entire L-region of the genome.

Gene ·Vol. 25 ·No. 2-3 ·1983-11-00 ·Pages 281-9

Knust E, Schirm S, Dietrich W, Bodemer W, Kolb E, Fleckenstein B

Abstract

Purified particles of Herpesvirus saimiri, a potent tumor-eliciting virus of primates, contain genomic DNA molecules (145-170 kb) consisting of a unique L-DNA region (112 kb) which is flanked by variable stretches of repetitive sequences (H-DNA). Restriction fragments representing the entire L-DNA of H. saimiri strain No. 11 were cloned in plasmid and bacteriophage vectors. The internal fragments of L-DNA generated by the enzymes EcoRI and KpnI were inserted into plasmid pACYC184, cosmid pJC81, or bacteriophage lambda derivative Charon 4A. The terminal parts of L-DNA, including the junctions between repetitive DNA and unique sequences, were cloned between the cleavage sites for KpnI and SmaI in the plasmid vector pWD7, which was constructed for this purpose. Molecular cloning allowed us to confirm and modify, in part, the existing cleavage maps of H. saimiri DNA. It provides a basis for future studies on virus replication and oncogenic transformation.

MeSH Terms
Bacteriophage lambda Cloning, Molecular DNA, Viral/biosynthesis Genes, Viral Herpesviridae/genetics Nucleic Acid Hybridization Plasmids Virus Cultivation
Chemicals
DNA, Viral
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Knust E
Schirm S
Dietrich W
Bodemer W
Kolb E
Fleckenstein B
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1983-11-00
Pages
281-9
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
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