Heat shock regulatory gene (htpR) of Escherichia coli is required for growth at high temperature but is dispensable at low temperature.
- 1 November 1984
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 81 (21) , 6803-6807
- https://doi.org/10.1073/pnas.81.21.6803
Abstract
Nonsense mutations affecting the positive regulatory gene (htpR) of heat shock response have been obtained in a strain of Escherichia coli carrying no suppressor. The mutants can grow only at temperatures below 34 degrees C-35 degrees C. Heat, ethanol, and coumermycin induce major heat shock proteins in the wild-type but not in the htpR mutants. In contrast, the level of heat shock proteins synthesized at low temperature is unaffected. The htpR gene product is thus required for induction of heat shock proteins by heat or other stresses but not for their "basal-level" synthesis. Nucleotide sequence has been determined for the wild-type and the mutant alleles of htpR. The coding region appears to consist of 852 nucleotide pairs that correspond to 284 amino acids. Sequences commonly considered as signals for transcriptional initiation and termination were found flanking the coding region. Within this region, six amber, one opal, and two missense mutations were identified; the nonsense mutations are scattered along the gene, some being very close to the presumed amino terminus. These results indicate that the absence of htpR gene product is directly responsible for the failure to respond to heat shock or other stresses and for the inability to grow at high temperature. We propose that htpR represents a new class of genes that are essential for growth only at high temperatures (greater than 35 degrees C). Implications of the sequence homologies found among htpR, rpoD, and nusA proteins are discussed.This publication has 23 references indexed in Scilit:
- Genetic control of heat-shock protein synthesis and its bearing on growth and thermal resistance in Escherichia coli K-12.Proceedings of the National Academy of Sciences, 1982
- Effects of reduced amount of RNA polymerase sigma factor on gene expression and growth of Escherichia coli: Studies of the rpoD40 (Amber) mutationMolecular Genetics and Genomics, 1981
- The nudeotide sequence of the cloned rpoD gene for the RNA polymerase sigma subunit from E. coil K12Nucleic Acids Research, 1981
- Interaction of the sigma factor and the nusA gene protein of E. coli with RNA polymerase in the initiation-termination cycle of transcriptionCell, 1981
- Positive regulatory gene for temperature-controlled proteins in Escherichia coliBiochemical and Biophysical Research Communications, 1981
- A system for shotgun DNA sequencingNucleic Acids Research, 1981
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977
- Evidence for a positive regulation of RNA polymerase synthesis in Escherichia coliJournal of Molecular Biology, 1975
- A temperature sensitive nonsense mutation affecting the synthesis of a major protein of Escherichia coli K12Molecular Genetics and Genomics, 1975
- Still more mutant tyrosine transfer ribonucleic acidsJournal of Molecular Biology, 1972