Cooperative Regulation of Campylobacter jejuni Heat-Shock Genes by HspR and HrcA

• Published in: Microorganisms (Basel) 2020-07, Vol.8 (8), p.1161
• Main Authors: Palombo, Marta, Scarlato, Vincenzo, Roncarati, Davide
• Format: Article
• Language: English
• Subjects: Binding sites; Campylobacter; Campylobacter jejuni; Circuits; Cloning; Deoxyribonuclease; Deoxyribonucleic acid; DNA; DNA/protein interaction; E coli; Evolutionary conservation; Gene expression; Gene sequencing; Genes; Genetic aspects; Genetic regulation; Genomes; Glycerol; Heat; Heat shock proteins; heat-shock response; Homology; HrcA repressor; HspR repressor; Inverted repeat; Molecular modelling; Nucleotide sequence; Observations; Pathogens; Physiological aspects; Plasmids; Preservation; Promoters; Repressors; RNA polymerase; Transcription factors; transcriptional regulation
• ISSN: 2076-2607; 2076-2607
• DOI: 10.3390/microorganisms8081161

The heat-shock response is defined by the transient gene-expression program that leads to the rapid accumulation of heat-shock proteins. This evolutionary conserved response aims at the preservation of the intracellular environment and represents a crucial pathway during the establishment of host–pathogen interaction. In the food-borne pathogen Campylobacter jejuni two transcriptional repressors, named HspR and HrcA, are involved in the regulation of the major heat-shock genes. However, the molecular mechanism underpinning HspR and HrcA regulatory function has not been defined yet. In the present work, we assayed and mapped the HspR and HrcA interactions on heat-shock promoters by high-resolution DNase I footprintings, defining their regulatory circuit, which governs C. jejuni heat-shock response. We found that, while DNA-binding of HrcA covers a compact region enclosing a single inverted repeat similar to the so-called Controlling Inverted Repeat of Chaperone Expression (CIRCE) sequence, HspR interacts with multiple high- and low-affinity binding sites, which contain HspR Associated Inverted Repeat (HAIR)-like sequences. We also explored the DNA-binding properties of the two repressors competitively on their common targets and observed, for the first time, that HrcA and HspR can directly interact and their binding on co-regulated promoters occurs in a cooperative manner. This mutual cooperative mechanism of DNA binding could explain the synergic repressive effect of HspR and HrcA observed in vivo on co-regulated promoters. Peculiarities of the molecular mechanisms exerted by HspR and HrcA in C. jejuni are compared to the closely related bacterium H. pylori that uses homologues of the two regulators.