Affiliation:
1. Department of Genetics, Estonian Biocentre and Institute of Molecular and Cell Biology, Tartu University, 51010 Tartu, Estonia
Abstract
ABSTRACT
Transposition is a DNA reorganization reaction potentially deleterious for the host. The frequency of transposition is limited by the amount of transposase. Therefore, strict regulation of a transposase is required to keep control over the destructive multiplication of the mobile element. We have shown previously that the expression of the transposase (
tnpA
) of the
Pseudomonas putida
PaW85 transposon Tn
4652
is positively affected by integration host factor. Here, we present evidence that the amount of the transposase of Tn
4652
in
P. putida
cells is controlled by the transposon-encoded protein (TnpC). Sequence analysis of the 120-amino-acid-long TnpC, coded just downstream of the
tnpA
gene, showed that it has remarkable similarity to the putative polypeptide encoded by the mercury resistance transposon Tn
5041
. As determined by quantitative Western blot analysis, the abundance of TnpA was reduced up to 10-fold in the intact
tnpC
background. In vivo experiments using transcriptional and translational fusions of the
tnpA
gene and the reporter gene
gusA
indicated that TnpC operates in the regulation of the transposase of Tn
4652
at the post-transcriptional level.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
16 articles.
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