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Open AccessJournal ArticleDOI

Sequence analysis and regulation of the htrA gene of Escherichin coli: a σ32-independent mechanism of heat-inducible transcription

Barbara Lipinska, +2 more
- 11 Nov 1988 - 
- Vol. 16, Iss: 21, pp 10053-10067
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TLDR
The htrA promoter is identified and it is found that it is similar to the P3 promoter of the rpoH gene, which encodes the sigma 32 RNA polymerase subunit and is known to regulate transcription of typical heat shock genes.
Abstract
Previous work has established that the E. coli htrA gene product is essential for bacterial survival at temperatures above 42 degrees. We have sequenced the htrA gene region and found an open reading frame (ORF) coding for a protein of 491 amino acids with a calculated molecular weight of 51,163 daltons. This molecular weight corresponds well with that seen following electrophoresis on SDS-polyacrylamide gels. This protein has an amino-terminal sequence typical for a leader peptide and undergoes post-translational modification by cleavage of an amino-terminal portion. The insertional mutations which affect the function of the htrA gene map inside this ORF. The levels of htrA mRNA increase rapidly and transiently upon heat shock in a manner independent of the rpoH gene, which encodes the sigma 32 RNA polymerase subunit and is known to regulate transcription of typical heat shock genes. Using S1 mapping and RNA primer extension, we have identified the htrA promoter and found that it is similar to the P3 promoter of the rpoH gene. The P3 promoter is especially active at high temperatures and is recognized by a recently identified transcriptional factor, sigma E.

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Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia.

TL;DR: This review summarizes the latest advances in understanding host-pathogen interactions in CF with an emphasis on the role and control of conversion to mucoidy in P. aeruginosa and B. cepacia.
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A Serine Protease, HtrA2, Is Released from the Mitochondria and Interacts with XIAP, Inducing Cell Death

TL;DR: HtrA2 is a Smac-like inhibitor of IAP activity with a serine protease-dependent cell death-inducing activity, which is neither accompanied by a significant increase in caspase activity nor inhibited by casp enzyme inhibitors, including XIAP.
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A temperature-dependent switch from chaperone to protease in a widely conserved heat shock protein.

TL;DR: It is shown here that the widely conserved heat shock protein DegP (HtrA) has both general molecular chaperone and proteolytic activities, which mean that a single cellular factor can switch between two key pathways, controlling protein stability and turnover.
Book ChapterDOI

The extracytoplasmic function (ECF) sigma factors.

TL;DR: Current knowledge of some of the better characterized extracytoplasmic function (ECF) sigma factors are reviewed, the variety of experimental approaches that have proven productive in defining the roles of ECF s Sigma factors are discussed, and some unifying themes that are beginning to emerge as more systems are studied are presented.
Journal ArticleDOI

The HtrA Family of Proteases: Implications for Protein Composition and Cell Fate

TL;DR: In this article, the authors discuss the properties and roles of the HtrA chaperone system in protein metabolism and cell fate, and discuss the role of this ATP-independent protease in protein degradation.
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