Recovery of a hybrid vector derived from bovine papilloma virus DNA pBR322 and the HSV tk gene by bacterial transformation with extrachromosomal DNA from transfected rodent cells

Takeshi Sekiguchi, Nishimoto Takeharu, Kai Ryosuke, Sekiguchi Mutsuo

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

A bovine papilloma virus (BPV)-pBR322-derived recombinant plasmid carrying a 2-kb fragment of Herpes simplex virus DNA containing the thymidine kinase (tk) gene is capable of transforming tk cells of mouse L and Syrian hamster BHK21 lines to tk+. In transformed cells a small proportion of the plasmid DNA is present as extrachromosomal elements while the remainder appears to be integrated into the genome. It was possible to recover plasmids indistinguishable from the input DNA by transformation of Escherichia coli bacteria with low-molecular-weight DNA isolated from the transformed mouse and hamster cells and consisting of BPV-pBR322-HSV tk+ plasmids.

Original languageEnglish
Pages (from-to)267-272
Number of pages6
JournalGene
Volume21
Issue number3
DOIs
Publication statusPublished - Jan 1 1983

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Bacterial Transformation
DNA Viruses
Thymidine Kinase
Papilloma
Rodentia
Plasmids
DNA
Genes
Viruses
Mesocricetus
Simplexvirus
Cricetinae
Molecular Weight
Genome
Escherichia coli
Bacteria

All Science Journal Classification (ASJC) codes

  • Genetics

Cite this

Recovery of a hybrid vector derived from bovine papilloma virus DNA pBR322 and the HSV tk gene by bacterial transformation with extrachromosomal DNA from transfected rodent cells. / Sekiguchi, Takeshi; Takeharu, Nishimoto; Ryosuke, Kai; Mutsuo, Sekiguchi.

In: Gene, Vol. 21, No. 3, 01.01.1983, p. 267-272.

Research output: Contribution to journalArticle

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