Abstract
AbstractThe small RNA (sRNA) RydC strongly activatescfa, which encodes the cyclopropane fatty acid synthase. Previous work demonstrated that RydC activation ofcfaincreases conversion of unsaturated fatty acids to cyclopropanated fatty acids in membrane lipids and changes the biophysical properties of membranes, making cells more resistant to acid stress. The conditions and regulators that control RydC synthesis had not previously been identified. In this study, we demonstrate that RydC regulation ofcfais important for resistance to membrane-disrupting conditions. We identify a GntR-family transcription factor, YieP, that repressesrydCtranscription and show that YieP indirectly regulatescfathrough RydC. YieP positively autoregulates its own transcription. We further identify additional sRNA regulatory inputs that contribute to control of RydC andcfa. The translation ofyiePis repressed by the Fnr-dependent sRNA, FnrS, making FnrS an indirect activator ofrydCandcfa.Conversely, RydC activity oncfais antagonized by the OmpR-dependent sRNA OmrB. Altogether, this work illuminates a complex regulatory network involving transcriptional and post-transcriptional inputs that link control of membrane biophysical properties to multiple environmental signals.ImportanceBacteria experience many environmental stresses that challenge their membrane integrity. To withstand these challenges, bacteria sense what stress is occurring and mount a response that protects membranes. Previous work documented the important roles of small RNA (sRNA) regulators in membrane stress responses. One sRNA, RydC, helps cells cope with membrane-disrupting stresses by promoting changes in the types of lipids incorporated into membranes. In this study, we identified a regulator, YieP, that controls when RydC is produced, and additional sRNA regulators that modulate YieP levels and RydC activity. These findings illuminate a complex regulatory network that helps bacteria sense and respond to membrane stress.
Publisher
Cold Spring Harbor Laboratory