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J. Bacteriol., 06 1996, 3201-3206, Vol 178, No. 11
JA Bogan and CE Helmstetter
The potential role of mioC transcription as a negative regulator of
initiation of chromosome replication in Escherichia coli was evaluated.
When initiation was aligned by a shift of dnaC2(Ts) mutants to
nonpermissive temperature (40 degrees C), mioC transcript levels measured
at the 5' end or reading through oriC disappeared within one mass doubling.
Upon return to permissive temperature (30 degrees C), the transcripts
reappeared coordinately about 15 min after the first synchronized
initiation and then declined sharply again 10 min later, just before the
second initiation. Although these observations were consistent with the
idea that mioC transcription might have to be terminated prior to
initiation, it was found that the interval between initiations at
permissive temperature, i.e., the eclipse period, was not influenced by the
time required to shut down mioC transcription, since the eclipse was the
same for chromosomes and minichromosomes which lacked mioC transcription.
This finding did not, in itself, rule out the possibility that mioC
transcription must be terminated prior to initiation of replication, since
it might normally be shut off before initiation, and never be limiting,
even during the eclipse. Therefore, experiments were performed to determine
whether the continued presence of mioC transcription during the process of
initiation altered the timing of initiation. It was found that
minichromosomes possessing a deletion in the DnaA box upstream of the
promoter transcribed mioC continuously and replicated with the same timing
as those that either shut down expression prior to initiation or lacked
expression entirely. It was further shown that mioC transcription was
present throughout the induction of initiation by addition of
chloramphenicol to a dnaA5(Ts) mutant growing at a semipermissive
temperature. Thus, transcription through oriC emanating from the mioC gene
promoter is normally inhibited prior to initiation of replication by the
binding of DnaA protein, but replication can initiate with the proper
timing even when transcription is not shut down; i.e., mioC does not serve
as a negative regulator of initiation. It is proposed, however, that the
reappearance and subsequent disappearance of mioC transcription during a
10-min interval at the end of the eclipse serves as an index of the minimum
time required for the establishment of active protein-DNA complexes at the
DnaA boxes in the fully methylated origin region of the chromosome. On this
basis, the eclipse constitutes the time for methylation of the newly formed
DNA strands (15 to 20 min at 30 degrees C) followed by the time for DnaA
protein to bind and activate oriC for replication (10 min).
Copyright © 1996, American Society for Microbiology
mioC transcription, initiation of replication, and the eclipse in Escherichia coli
Department of Biological Sciences, Florida Institute of Technology, Melbourne, 32901, USA.
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