THE ESCHERICHIA-COLI HEAT-SHOCK GENE HTPY - MUTATIONAL ANALYSIS, CLONING, SEQUENCING, AND TRANSCRIPTIONAL REGULATION

Citation
D. Missiakas et al., THE ESCHERICHIA-COLI HEAT-SHOCK GENE HTPY - MUTATIONAL ANALYSIS, CLONING, SEQUENCING, AND TRANSCRIPTIONAL REGULATION, Journal of bacteriology, 175(9), 1993, pp. 2613-2624
Citations number
42
Categorie Soggetti
Microbiology
Journal title
ISSN journal
00219193
Volume
175
Issue
9
Year of publication
1993
Pages
2613 - 2624
Database
ISI
SICI code
0021-9193(1993)175:9<2613:TEHGH->2.0.ZU;2-S
Abstract
We have identified a new heat shock gene, designated htpY, located 700 bp upstream of the dnaK dnaJ operon. We cloned it and showed that it is transcribed clockwise vis-a-vis the Escherichia coli genetic map, i n the same direction as the dnaK dnaJ operon. The htpY gene encodes a 21,193-Da polypeptide. Promoter mapping experiments and Northern (RNA) analysis showed that the htpY gene belongs to the classical heat shoc k gene family, because the transcription from its major promoter is un der the positive control of the rpoH gene prodUCt (sigma32) and resemb les canonical Esigma32-transcribed consensus promoter sequences. This conclusion has been strengthened by the construction and analysis of a phtpY-lacZ promoter fusion. Despite the fact that htpY null bacteria are viable, the expression of various Esigma32 heat shock promoters is significantly decreased, suggesting that HtpY plays an important role in the regulation of the heat shock response. Consistent with this in terpretation, overproduction of the HtpY protein results in a generali zed increase of the heat shock response in E. coli.