GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.

Have any questions? Please email us at ecoliwiki@gmail.com

PMID:6436819

From GONUTS
Jump to: navigation, search
Citation

Goff, SA, Casson, LP and Goldberg, AL (1984) Heat shock regulatory gene htpR influences rates of protein degradation and expression of the lon gene in Escherichia coli. Proc. Natl. Acad. Sci. U.S.A. 81:6647-51

Abstract

Upon a shift to high temperature, Escherichia coli increase their rate of protein degradation and also the expression of a set of "heat shock" genes. Nonsense mutants of htpR (also called hin), suppressed by a temperature-sensitive suppressor, show lower expression of heat shock genes at 30 degrees C and fail to respond to a shift to 42 degrees C. These mutants were found to have a lower capacity to degrade abnormal or incomplete proteins than that of wild-type cells. This reduction in proteolysis equals or exceeds that in lon mutants, which encode a defective ATP-dependent protease, protease La, and is particularly large in htpR lon double mutants. The activity of protease La was higher in wild-type cells than in htpR mutants grown at 30 degrees C and increased upon shift to 42 degrees C only in the wild type. To determine whether htpR influences transcription of the lon gene, a lon-lacZ operon fusion was utilized. Introduction of the htpR mutation reduced transcription from the lon promoter at 30 degrees C and 37 degrees C. This defect was corrected by a plasmid (pFN97) carrying the wild-type htpR allele. Induction of the heat shock response with ethanol had little or no effect in htpR mutants but stimulated lon transcription 2-3 fold in wild-type cells and htpR cells carrying pFN97. Thus, lon appears to be a heat shock gene, and increased synthesis of protease La under stressful conditions may help to prevent the accumulation of damaged cellular protein.

Links

PubMed PMC391987

Keywords

ATP-Dependent Proteases; Adenosine Triphosphate/pharmacology; Bacterial Proteins/metabolism; DNA, Recombinant; Endopeptidases/metabolism; Escherichia coli/genetics; Escherichia coli/metabolism; Escherichia coli Proteins; Genes, Bacterial; Genes, Regulator; Heat-Shock Proteins/genetics; Hot Temperature; Lac Operon; Mutation; Operon; Phenotype; Protease La; Serine Endopeptidases; Transcription, Genetic; beta-Galactosidase/metabolism

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

ECOLI:LON

GO:0009408: response to heat

ECO:0000270:

P

Table 1. shows upregulation of Lon in response to heat exposure (42C)

complete

ECOLI:LON

GO:0009411: response to UV

ECO:0000315:

P

Table 3. Increased UV sensitivity in mutant lon

complete

ECOLI:LON

GO:0006508: proteolysis

ECO:0000315:

P

Fig. 1 and 2 show decreased proteolytic activity in the mutant phenotype

complete

ECOLI:LON

GO:0045471: response to ethanol

ECO:0000270:

P

Table 1. shows enhanced Lon expression in the presence of ethanol (4%)

complete


See also

References

See Help:References for how to manage references in GONUTS.