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Journal of Bacteriology, October 1999, p. 6312-6318, Vol. 181, No. 20
Department of Genetics, Estonian Biocentre
and Institute of Molecular and Cell Biology, Tartu University,
51010 Tartu, Estonia
Received 17 May 1999/Accepted 11 August 1999
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 Tn4652 is
positively affected by integration host factor. Here, we present
evidence that the amount of the transposase of Tn4652 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 Tn5041. 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
Tn4652 at the post-transcriptional level.
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Regulation of the Transposase of Tn4652
by the Transposon-Encoded Protein TnpC
*
Corresponding author. Mailing address: Estonian
Biocentre and Institute of Molecular and Cell Biology, Tartu
University, 23 Riia Street, 51010 Tartu, Estonia. Phone: 372-7-375015. Fax: 372-7-420286. E-mail: rhorak{at}ebc.ee.
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