The transcriptional repressor CcpN from Bacillus subtilis mediates the CcpA-independent catabolite repression of three genes, sr1, encoding a small regulatory RNA, and two gluconeogenesis genes, gapB and pckA. The intracellular concentration of CcpN was determined to be around 4000 molecules per cell. The B. subtilis genome was scanned for potential new CcpN target genes, out of which three showed CcpN-binding activity in their upstream region. EMSAs (electrophoretic mobility shift assays) demonstrated that the promoter regions of two putative targets, thyB encoding thymidylate synthase B and yhaM encoding a 5'-3' exo-RNAse, bound CcpN with significant affinity. A detailed contact probing of CcpN-DNA interactions revealed an interesting new binding pattern at the thyB promoter, where the whole promoter appears to be contacted by CcpN. Using lacZ-reporter gene fusions and in vitro transcription assays, the thyB promoter was investigated for a regulatory effect of CcpN. Surprisingly, CcpN does not repress transcription at this promoter, but instead acts as an activator. Alignments of the thyB promoters of different Gram-positive bacteria encoding CcpN revealed CcpN consensus-binding sites in a significant number of them. Our data show that a bioinformatics-based approach combined with in vivo and in vitro experiments can be used to identify new targets of transcriptional regulators.

Regulatory small RNAs (sRNAs) in bacterial genomes have become a focus of research over the past 8 years. Whereas more than 100 such sRNAs have been found in Escherichia coli, relatively little is known about sRNAs in gram-positive bacteria. Using a computational approach, we identified two sRNAs in intergenic regions of the Bacillus subtilis genome, SR1 and SR2 (renamed BsrF). Recently, we demonstrated that SR1 inhibits the translation initiation of the transcriptional activator AhrC. Here, we describe detection of BsrF, its expression profile, and its regulation by CodY. Furthermore, we mapped the secondary structure of BsrF. BsrF is expressed in complex and minimal media in all growth phases in B. subtilis and, with a similar expression profile, also in Bacillus amyloliquefaciens. Neither overexpression nor deletion of bsrF affected the growth of B. subtilis. BsrF was found to be long-lived in complex and minimal media. Analysis of 13 putative transcription factor binding sites upstream of bsrF revealed only an effect for CodY. Here, we showed by using Northern blotting, lacZ reporter gene fusions, in vitro transcription, and DNase I footprinting that the transcription of bsrF is activated by CodY in the presence of branched-chain amino acids and GTP. Furthermore, BsrF transcription was increased 1.5- to 2-fold by glucose in the presence of branched-chain amino acids, and this increase was independent of the known glucose-dependent regulators. BsrF is the second target for which transcriptional activation by CodY has been discovered.