Mutations that affect Tn5 insertion into pBR322: importance of local DNA supercoiling
- 1 October 1990
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 172 (10) , 5956-5960
- https://doi.org/10.1128/jb.172.10.5956-5960.1990
Abstract
The major hot spot of transposon Tn5 insertion in plasmid pBR322 (hot spot I) is in the promoter for the tetracycline resistance gene (tet). We made a series of pBR322 derivatives with mutations in and around this promoter and assayed their effects on insertion of Tn5 into hot spot I. Those mutations which reduced transcription from the tet promoter also reduced the frequency of insertion into hot spot I. Transcription and translation of tet are thought to cause the formation of paired domains of negative and positive supercoiling in pBR322. An amber codon in tet, 345 base pairs from hot spot I, decreases the negative supercoiling of the DNA segment containing hot spot I because it terminates translation of tet prematurely. We report here that this amber mutation also reduces insertion into hot spot I. These results suggest that the ability of Tn5 to insert into its major hot spot in pBR322 depends directly on negative supercoiling of the target DNA.This publication has 31 references indexed in Scilit:
- Tetracycline promoter mutations decrease non-B DNA structural transitions, negative linking differences and deletions in recombinant plasmids in Escherichia coliJournal of Molecular Biology, 1989
- Transcription generates positively and negatively supercoiled domains in the templateCell, 1988
- Escherichia coli integration host factor binds specifically to the ends of the insertion sequence IS1 and to its major insertion hot-spot in pBR322Journal of Molecular Biology, 1987
- Plasmid vector pBR322 and its special-purpose derivatives — a reviewGene, 1986
- Nonrandom insertion of Tn5 into cloned human adeno virus DNAGene, 1985
- DNA gyrase is a host factor required for transposition of Tn5Cell, 1982
- A symmetrical six-base-pair target site sequence determines Tn10 insertion specificityCell, 1982
- Studies on Transposition Mechanisms and Specificity of IS4Cold Spring Harbor Symposia on Quantitative Biology, 1981
- Analysis of gene control signals by DNA fusion and cloning in Escherichia coliJournal of Molecular Biology, 1980
- Internal Structure of the Nucleosome: DNA Folding in the Conserved 140-Base-pair Core ParticleCold Spring Harbor Symposia on Quantitative Biology, 1978