CsrA activates flhDC expression by protecting flhDC mRNA from RNase E-mediated cleavage

Authors

  • Alexander V. Yakhnin,

    1. Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, PA, USA
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    • These authors contributed equally to the work.
  • Carol S. Baker,

    1. Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, PA, USA
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    • These authors contributed equally to the work.
  • Christopher A. Vakulskas,

    1. Department of Microbiology and Cell Science, University of Florida, Gainesville, FL, USA
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  • Helen Yakhnin,

    1. Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, PA, USA
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  • Igor Berezin,

    1. Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, PA, USA
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  • Tony Romeo,

    1. Department of Microbiology and Cell Science, University of Florida, Gainesville, FL, USA
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  • Paul Babitzke

    Corresponding author
    • Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, PA, USA
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For correspondence. E-mail pxb28@psu.edu; Tel. (+1) 814 865 0002; Fax (+1) 814 863 7024.

Summary

Csr is a conserved global regulatory system that controls expression of several hundred Escherichia coli genes. CsrA protein represses translation of numerous genes by binding to mRNA and inhibiting ribosome access. CsrA also activates gene expression, although an activation mechanism has not been reported. CsrA activates flhDC expression, encoding the master regulator of flagellum biosynthesis and chemotaxis, by stabilizing the mRNA. Computer modelling, gel mobility shift and footprint analyses identified two CsrA binding sites extending from positions 1–12 (BS1) and 44–55 (BS2) of the 198 nt flhDC leader transcript. flhD′–′lacZ expression was reduced by mutations in csrA and/or the CsrA binding sites. The position of BS1 suggested that bound CsrA might inhibit 5′ end-dependent RNase E cleavage of flhDC mRNA. Consistent with this hypothesis, CsrA protected flhDC leader RNA from RNase E cleavage in vitro and protection depended on BS1 and BS2. Primer extension studies identified flhDC decay intermediates in vivo that correspond to in vitro RNase E cleavage sites. Deletion of these RNase E cleavage sites resulted in increased flhD′–′lacZ expression. Data from mRNA decay studies and quantitative primer extension assays support a model in which bound CsrA activates flhDC expression by inhibiting the 5′ end-dependent RNase E cleavage pathway.

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