Correlation Engine 2.0
Clear Search sequence regions


  • bacteria (2)
  • exoribonucleases (2)
  • gene (5)
  • gram (1)
  • human (2)
  • protein biosynthesis (1)
  • protein control (1)
  • R (10)
  • ribosomes (1)
  • rna (7)
  • rnr (1)
  • secG (2)
  • small protein b (1)
  • SmpB (8)
  • SsrA (2)
  • streptococcus (3)
  • stress- protein (1)
  • transfer- rna (1)
  • Sizes of these terms reflect their relevance to your search.

    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. 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. 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.

    Citation

    Ricardo N Moreira, Susana Domingues, Sandra C Viegas, Mónica Amblar, Cecília M Arraiano. Synergies between RNA degradation and trans-translation in Streptococcus pneumoniae: cross regulation and co-transcription of RNase R and SmpB. BMC microbiology. 2012 Nov 20;12:268

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 23167513

    View Full Text