Faculty Opinions recommendation of Regulation of the alternative sigma factor sigma(E) during initiation, adaptation, and shutoff of the extracytoplasmic heat shock response in Escherichia coli.

Author(s):  
Juan Luis Ramos
2022 ◽  
Vol 12 ◽  
Author(s):  
Yehong Huang ◽  
Wurihan Wurihan ◽  
Bin Lu ◽  
Yi Zou ◽  
Yuxuan Wang ◽  
...  

Cells reprogram their transcriptome in response to stress, such as heat shock. In free-living bacteria, the transcriptomic reprogramming is mediated by increased DNA-binding activity of heat shock sigma factors and activation of genes normally repressed by heat-induced transcription factors. In this study, we performed transcriptomic analyses to investigate heat shock response in the obligate intracellular bacterium Chlamydia trachomatis, whose genome encodes only three sigma factors and a single heat-induced transcription factor. Nearly one-third of C. trachomatis genes showed statistically significant (≥1.5-fold) expression changes 30 min after shifting from 37 to 45°C. Notably, chromosomal genes encoding chaperones, energy metabolism enzymes, type III secretion proteins, as well as most plasmid-encoded genes, were differentially upregulated. In contrast, genes with functions in protein synthesis were disproportionately downregulated. These findings suggest that facilitating protein folding, increasing energy production, manipulating host activities, upregulating plasmid-encoded gene expression, and decreasing general protein synthesis helps facilitate C. trachomatis survival under stress. In addition to relieving negative regulation by the heat-inducible transcriptional repressor HrcA, heat shock upregulated the chlamydial primary sigma factor σ66 and an alternative sigma factor σ28. Interestingly, we show for the first time that heat shock downregulates the other alternative sigma factor σ54 in a bacterium. Downregulation of σ54 was accompanied by increased expression of the σ54 RNA polymerase activator AtoC, thus suggesting a unique regulatory mechanism for reestablishing normal expression of select σ54 target genes. Taken together, our findings reveal that C. trachomatis utilizes multiple novel survival strategies to cope with environmental stress and even to replicate. Future strategies that can specifically target and disrupt Chlamydia’s heat shock response will likely be of therapeutic value.


1995 ◽  
Vol 14 (5) ◽  
pp. 1043-1055 ◽  
Author(s):  
S. Raina ◽  
D. Missiakas ◽  
C. Georgopoulos

1986 ◽  
Vol 83 (18) ◽  
pp. 6959-6963 ◽  
Author(s):  
T. Tsuchido ◽  
R. A. VanBogelen ◽  
F. C. Neidhardt

1987 ◽  
Vol 169 (2) ◽  
pp. 885-887 ◽  
Author(s):  
D Taglicht ◽  
E Padan ◽  
A B Oppenheim ◽  
S Schuldiner

2019 ◽  
Author(s):  
Christopher R. Evans ◽  
Yongqiang Fan ◽  
Jiqiang Ling

AbstractThe misincorporation of an incorrect amino acid into a polypeptide during protein synthesis is considered a detrimental phenomenon. Mistranslated protein is often misfolded and degraded or non-functional and results in an increased cost to quality control machinery. Despite these costs, errors during protein synthesis are common in bacteria. Here we report that increased rates of mistranslation inEscherichia coliprovide protection from protein misfolding stress by increasing the level of the heat shock sigma factor, RpoH. Surprisingly, this increase in RpoH due to mistranslation is dependent on the presence of the general stress response sigma factor, RpoS. This report provides evidence for a protective function of mistranslation and suggests a novel regulatory role of RpoS on the RpoH-activated heat shock.


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