Small RNAs endow a transcriptional activator with essential repressor functions for single-tier control of a global stress regulon

The Escherichia coli sigma(E) envelope stress response monitors and repairs the outer membrane, a function central to the life of Gram-negative bacteria. The sigma(E) stress response was characterized as a single-tier activation network comprised of similar to 100 genes, including the MicA and RybB noncoding sRNAs. These highly expressed sRNAs were thought to carry out the specialized function of halting de novo synthesis of several abundant porins when envelope homeostasis was perturbed. Using a systematic target profiling and validation approach we discovered that MicA and RybB are each global mRNA repressors of both distinct and shared targets, and that the two sRNAs constitute a posttranscriptional repression arm whose regulatory scope rivals that of the protein-based sigma(E) activation arm. Intriguingly, porin mRNAs constitute only similar to 1/3 of all targets and new nonporin targets predict roles for MicA and RybB in crosstalk with other regulatory responses. This work also provides an example of evolutionarily unrelated sRNAs that are coinduced and bind the same targets, but at different sites. Our finding that expression of either MicA or RybB sRNA protects the cell from the loss of viability experienced when sigma(E) activity is inadequate illustrates the importance of the posttranscriptional repression arm of the response. sigma(E) is a paradigm of a single-tier stress response with a clear division of labor in which highly expressed noncoding RNAs (MicA, RybB) endow a transcriptional factor intrinsically restricted to gene activation (sigma(E)) with the opposite repressor function.