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J. Biol. Chem., Vol. 266, Issue 6, 3774-3781, 02, 1991
K Asano, A Kato, H Moriwaki, C Hama, K Shiba and K Mizobuchi
Expression of the repZ gene involved in DNA replication of the ColIb-P9
plasmid depends on translation of a transcribed repZ leader sequence (repY)
and is negatively regulated by Inc RNA, the product of the inc gene and a
countertranscript to RepZ mRNA. To further understand the regulatory loop
of repZ expression, we isolated and characterized replication-defective
ColIb-P9 mutants that affected the level of repZ expression. Here we report
that mutations occurring in two complementary sequences, one (5'GGCG3') in
the inc region and one in the repY region, reduce the level of repZ
expression without affecting transcription. The mutations in one
complementary sequence were suppressed by compensatory base changes in the
other sequence, restoring the ability of repZ expression. These results
indicated that interaction by base pairing between the two complementary
sequences of RepZ mRNA was essential for repZ translation. The two
sequences, separated by 107 bases from each other, have a potential to form
a novel pseudoknot in the RepZ mRNA leader. We also found that some
mutations in the 5'GGCG3' sequence altered the specificity of Inc RNA,
thereby reducing significantly its regulatory activity. Thus, this single
specific sequence is involved in both positive and negative regulations for
repZ expression. Possible regulatory mechanisms of repZ expression are
discussed.
Positive and negative regulations of plasmid CoLIb-P9 repZ gene expression at the translational level
Department of Biophysics and Biochemistry, Faculty of Science, University of Tokyo, Hongo, Japan.
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