Conserved and Variable Functions of the σE Stress Response in Related Genomes

TLDR

Bacteria use alternative sigma factors to direct RNA polymerase to stress‑response genes, but promoter variability and motif spacing make predicting these regulons difficult. The study aims to elucidate conserved and organism‑specific functions of sigma factors by enabling promoter prediction to trace regulons across species. We built and validated an accurate promoter prediction model for E. coli sigmaE, identifying 89 unique sigmaE‑controlled transcription units in K‑12 and eight related genomes.

Abstract

Bacteria often cope with environmental stress by inducing alternative sigma (sigma) factors, which direct RNA polymerase to specific promoters, thereby inducing a set of genes called a regulon to combat the stress. To understand the conserved and organism-specific functions of each sigma, it is necessary to be able to predict their promoters, so that their regulons can be followed across species. However, the variability of promoter sequences and motif spacing makes their prediction difficult. We developed and validated an accurate promoter prediction model for Escherichia coli sigmaE, which enabled us to predict a total of 89 unique sigmaE-controlled transcription units in E. coli K-12 and eight related genomes. SigmaE controls the envelope stress response in E. coli K-12. The portion of the regulon conserved across genomes is functionally coherent, ensuring the synthesis, assembly, and homeostasis of lipopolysaccharide and outer membrane porins, the key constituents of the outer membrane of Gram-negative bacteria. The larger variable portion is predicted to perform pathogenesis-associated functions, suggesting that sigmaE provides organism-specific functions necessary for optimal host interaction. The success of our promoter prediction model for sigmaE suggests that it will be applicable for the prediction of promoter elements for many alternative sigma factors.