Joel Duff
Abstract below:
Vol. 96, Issue 9, 5089-5094, April 27, 1999
Hypermutation in derepressed operons of Escherichia coli K12
(stringent response / transcription / mutations)
Barbara E. Wright*, Angelika Longacre, and Jacqueline M. Reimers
Division of Biological Sciences, University of Montana, Missoula, MT 59812
Communicated by E. R. Stadtman, National Heart, Lung and Blood Institute,
Bethesda, MD, February 16, 1999 (received for review December
15, 1998)
This article presents evidence that starvation for leucine in an
Escherichia coli auxotroph triggers metabolic activities that specifically
target the leu operon
for derepression, increased rates of transcription, and mutation.
Derepression of the leu operon was a prerequisite for its activation by the
signal nucleotide,
guanosine tetraphosphate, which accumulates in response to nutritional
stress (the stringent response). A quantitative correlation was established
between
leuB mRNA abundance and leuB reversion rates. To further demonstrate that
derepression increased mutation rates, the chromosomal leu operon was
placed under the control of the inducible tac promoter. When the leu operon
was induced by isopropyl-D-thiogalactoside, both leuB mRNA abundance and
leuB reversion rates increased. These investigations suggest that guanosine
tetraphosphate may contribute as much as attenuation in regulating leu
operon
expression and that higher rates of mutation are specifically associated
with the derepressed leu operon.