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PMID: 6305767 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mechanism of F factor-enhanced excision of transposon Tn5.

Gene ·Vol. 22 ·No. 1 ·1983-04-00 ·Pages 1-7

Berg DE, Egner C, Lowe JB

Abstract

The reversion of lac:: Tn5 insertion mutations was used to examine the control of excision of the kanamycin-resistance transposon Tn5 in Escherichia coli. Earlier work which showed that the fertility factor F enhances Tn5 excision had led another group to suggest that this is due to the product of a putative transposable element-specific "recombination" gene in the F factor which can act on Tn5 located anywhere in the genome. We show, however, that Tn5 is excised from sites in the lac operon of F'lac plasmids several orders of magnitude more efficiently than from the same sites in the chromosomes of F-, F+ or homozygous lac:: Tn5[F'lac:: Tn5] strains. Thus F enhances Tn5 excision, but only if F and Tn5 are in cis in the same DNA molecule. Bacterial crosses showed that transfer of F'lac:: Tn5 plasmids by conjugation stimulates Tn5 excision, and that transfer is frequent even within F' populations. These results suggest that the ability of F to enhance excision is the consequence of DNA transfer in conjugation.

MeSH Terms
Conjugation, Genetic DNA Transposable Elements DNA, Bacterial/genetics Escherichia coli/genetics F Factor Genes, Bacterial Mutation
Chemicals
DNA Transposable Elements DNA, Bacterial
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Berg D E
Egner C
Lowe J B
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1983-04-00
Pages
1-7
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
Grants
NIAID NIH HHS · 1 R01 AI 18980 · United States
NIAID NIH HHS · 5 R01 AI14267 · United States
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