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Journal of Bacteriology, December 2000, p. 6630-6637, Vol. 182, No. 23
Nelson Biological Laboratory, Rutgers, The State University
of New Jersey, Busch Campus, Piscataway, New Jersey
08854,1 and Department of Food
Science, Rutgers, The State University of New Jersey, Cook Campus,
New Brunswick, New Jersey 089012
Received 12 June 2000/Accepted 18 September 2000
Transcription of the clpP-clpX operon of
Escherichia coli leads to the production of two different
sizes of transcripts. In log phase, the level of the longer transcript
is higher than the level of the shorter transcript. Soon after the
onset of carbon starvation, the level of the shorter transcript
increases significantly, and the level of the longer transcript
decreases. The longer transcript consists of the entire
clpP-clpX operon, whereas the shorter transcript contains
the entire clpP gene but none of the clpX
coding sequence. The RpoH protein is required for the increase in the
level of the shorter transcript during carbon starvation. Primer
extension experiments suggest that there is increased usage of the
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Copyright © 2000, American Society for Microbiology. All rights reserved.
Expression of Different-Size Transcripts from the
clpP-clpX Operon of Escherichia coli during
Carbon Deprivation

and
32-dependent promoter of the clpP-clpX
operon within 15 min after the start of carbon starvation. Expression
of the clpP-clpX operon from the promoters upstream of the
clpP gene decreases to a very low level by 20 min after the
onset of carbon starvation. Various pieces of evidence suggest, though
they do not conclusively prove, that production of the shorter
transcript may involve premature termination of the longer transcript.
The half-life of the shorter transcript is much less than that of the
longer transcript during carbon starvation. E. coli rpoB
mutations that affect transcription termination efficiency alter the
ratio of the shorter clpP-clpX transcript to the longer
transcript. The E. coli rpoB3595 mutant, with an RNA
polymerase that terminates transcription with lower efficiency than the
wild type, accumulates a lower percentage of the shorter transcript
during carbon starvation than does the isogenic wild-type strain. In
contrast, the rpoB8 mutant, with an RNA polymerase that
terminates transcription with higher efficiency than the wild type,
produces a higher percentage of the shorter clpP-clpX
transcript when E. coli is in log phase. These and other data are consistent with the hypothesis that the shorter transcript results from premature transcription termination during production of
the longer transcript.
*
Corresponding author. Mailing address: Department of
Food Science, Rutgers, The State University of New Jersey, Cook Campus, 65 Dudley Road, New Brunswick, NJ 08901. Phone: (732) 932-3634. Fax:
(732) 932-6776. E-mail: lsimon{at}aesop.rutgers.edu.
Present address: Institute of Biomedical Sciences, Academia Sinica,
Nankang, Taipei 11529, Taiwan.
Present address: International Business Machines Corporation,
Montville East Corporate Center, Pine Brook, NJ 07058.
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