Growth phase-dependent control of transcription start site selection and gene expression by nanoRNAs

  1. Bryce E. Nickels1,2,7
  1. 1Waksman Institute, Rutgers University, Piscataway, New Jersey 08854, USA;
  2. 2Department of Genetics, Rutgers University, Piscataway, New Jersey 08854, USA;
  3. 3Division of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA;
  4. 4The Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, Massachusetts 02142, USA;
  5. 5Channing Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA
    1. 6 These authors contributed equally to this work.

    Abstract

    Prokaryotic and eukaryotic RNA polymerases can use 2- to ∼4-nt RNAs, “nanoRNAs,” to prime transcription initiation in vitro. It has been proposed that nanoRNA-mediated priming of transcription can likewise occur under physiological conditions in vivo and influence transcription start site selection and gene expression. However, no direct evidence of such regulation has been presented. Here we demonstrate in Escherichia coli that nanoRNAs prime transcription in a growth phase-dependent manner, resulting in alterations in transcription start site selection and changes in gene expression. We further define a sequence element that determines, in part, whether a promoter will be targeted by nanoRNA-mediated priming. By establishing that a significant fraction of transcription initiation is primed in living cells, our findings contradict the conventional model that all cellular transcription is initiated using nucleoside triphosphates (NTPs) only. In addition, our findings identify nanoRNAs as a previously undocumented class of regulatory small RNAs that function by being directly incorporated into a target transcript.

    Keywords

    Footnotes

    • Received March 23, 2012.
    • Accepted May 21, 2012.
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