Post-transcriptional controls in bacteriophage T4: roles of the sequence-specific endoribonuclease RegB

Authors

  • Bénédicte Sanson,

    1. CNRS URA1139, Institut de Biologie Physico-chimique 13, rue Pierre et Marie Curie, 75005 Paris, France
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  • Marc Uzan

    Corresponding author
    1. CNRS URA1139, Institut de Biologie Physico-chimique 13, rue Pierre et Marie Curie, 75005 Paris, France
      *Corresponding author. Tel.: +33 (1) 43 25 26 09; Fax: +33 (1) 40 46 83 31; E-mail: uzan@ibpc.fr
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*Corresponding author. Tel.: +33 (1) 43 25 26 09; Fax: +33 (1) 40 46 83 31; E-mail: uzan@ibpc.fr

Abstract

Abstract: Gene regB of bacteriophage T4 encodes a sequence-specific endoribonuclease which introduces cuts in early phage messenger RNAs. In most cases, cutting takes place in the middle of the tetranucleotide GGAG. Efficient cleavages occur in the motifs located in intergenic regions, some of them being Shine-Dalgarno sequences. When located in a coding sequence, this tetranucleotide is poorly recognized or not at all. In this article, we have reviewed the properties of the RegB endoribonuclease, with emphasis on its possible roles in T4 development. We show that the nuclease RegB plays at least two roles: (i) it inactivates a sub-class of early mRNA by cleaving Shine-Dalgarno sequences, and (ii) it is necessary for the degradationn of early mRNAs, but not of middle and late mRNAs. Accordingly, we found that middle and late mRNAs avoid processing by RegB, probably for different reasons. Most of the middle mRNAs (mRNAs initiated at MotA-dependent promoters) do not contain the motif GGAG in their intergenic regions, whereas about one-third of the late genes have this motif as Shine-Dalgarno sequence. It is not yet known whether the RNase is inactivated early in the phage cycle, or whether it remains active but cannot recognize late mRNAs as substrates.

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