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Journal of Bacteriology, November 2001, p. 6543-6550, Vol. 183, No. 22
Centre for Cellular and Molecular Biology,
Hyderabad 500 007,1 and Centre for DNA
Fingerprinting and Diagnostics, Hyderabad 500 076,2 India
Received 22 May 2001/Accepted 30 August 2001
Unlike the
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.22.6543-6550.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
In Vivo Expression from the RpoS-Dependent P1
Promoter of the Osmotically Regulated proU Operon in
Escherichia coli and Salmonella enterica
Serovar Typhimurium: Activation by rho and
hns Mutations and by Cold Stress
70-controlled P2 promoter for the
osmotically regulated proU operon of Escherichia
coli and Salmonella enterica serovar
Typhimurium, the
s-controlled P1 promoter situated
further upstream appears not to contribute to expression of the
proU structural genes under ordinary growth conditions.
For S. enterica proU P1, there is evidence that promoter crypticity is the result of a transcription attenuation phenomenon which is relieved by the deletion of a 22-base
C-rich segment in the transcript. In this study, we have sought to
identify growth conditions and trans-acting mutations which activate in vivo expression from proU P1. The
cryptic S. enterica proU P1 promoter was
activated, individually and additively, in a rho mutant
(which is defective in the transcription termination factor Rho) as
well as by growth at 10°C. The E. coli
proU P1 promoter was also cryptic in constructs that carried
1.2 kb of downstream proU sequence, and in these cases
activation of in vivo expression was achieved either by a
rho mutation during growth at 10°C or by an
hns null mutation (affecting the nucleoid protein H-NS)
at 30°C. The rho mutation had no effect at either 10 or 30°C on in vivo expression from two other
s-controlled promoters tested, those for
osmY and csiD. In cells lacking the
RNA-binding regulator protein Hfq, induction of E. coli proU P1 at 10°C and by hns
mutation at 30°C was still observed, although the hfq
mutation was associated with a reduction in the absolute levels of P1
expression. Our results suggest that expression from
proU P1 is modulated both by nucleoid structure and by
Rho-mediated transcription attenuation and that this promoter may be
physiologically important for proU operon expression
during low-temperature growth.
*
Corresponding author. Mailing address: Centre for DNA
Fingerprinting and Diagnostics, ECIL Road, Hyderabad 500 076, India. Phone: 91-40-7155609. Fax: 91-40-7155610. E-mail:
shankar{at}www.cdfd.org.in.
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