Key result
In Streptococcus pneumoniae, RNase R and SmpB are mutually dependent and cross-regulated, with RNase R expression induced under cold-shock and modulated by SmpB, while SmpB is controlled by RNase R.
These interactions may shape pneumococcal stress adaptation; leaves open roles in pathogenesis or therapeutic targeting.
BACKGROUND: Ribonuclease R (RNase R) is an exoribonuclease that recognizes and degrades a wide range of RNA molecules. It is a stress-induced protein shown to be important for the establishment of virulence in several pathogenic bacteria. RNase R has also been implicated in the trans-translation process. Transfer-messenger RNA (tmRNA/SsrA RNA) and SmpB are the main effectors of trans-translation, an RNA and protein quality control system that resolves challenges associated with stalled ribosomes on non-stop mRNAs. Trans-translation has also been associated with deficiencies in stress-response mechanisms and pathogenicity. RESULTS: In this work we study the expression of RNase R in the human pathogen Streptococcus pneumoniae and analyse the interplay of this enzyme with the main components of the trans-translation machinery (SmpB and tmRNA/SsrA). We show that RNase R is induced after a 37°C to 15°C temperature downshift and that its levels are dependent on SmpB. On the other hand, our results revealed a strong accumulation of the smpB transcript in the absence of RNase R at 15°C. Transcriptional analysis of the S. pneumoniae rnr gene demonstrated that it is co-transcribed with the flanking genes, secG and smpB. Transcription of these genes is driven from a promoter upstream of secG and the transcript is processed to yield mature independent mRNAs. This genetic organization seems to be a common feature of Gram positive bacteria, and the biological significance of this gene cluster is further discussed. CONCLUSIONS: This study unravels an additional contribution of RNase R to the trans-translation system by demonstrating that smpB is regulated by this exoribonuclease. RNase R in turn, is shown to be under the control of SmpB. These proteins are therefore mutually dependent and cross-regulated. The data presented here shed light on the interactions between RNase R, trans-translation and cold-shock response in an important human pathogen.
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Moreira et al. (2012) studied Streptococcus pneumoniae basic biology. Gene deletion and complementation (rnr and smpB) vs. Wild type Streptococcus pneumoniae was evaluated on Protein and mRNA expression levels. In Streptococcus pneumoniae, RNase R and SmpB are mutually dependent and cross-regulated, with RNase R expression induced under cold-shock and modulated by SmpB, while SmpB is controlled by RNase R.
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