A second riboswitch class for the enzyme cofactor NAD+

  1. Ronald R. Breaker1,3,4
  1. 1Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA
  2. 2Department of Chemistry, Yale University, New Haven, Connecticut 06520-8103, USA
  3. 3Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520-8103, USA
  4. 4Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520-8103, USA
  1. Corresponding author: ronald.breaker{at}yale.edu
  1. 5 These authors contributed equally to this work.

Abstract

A bacterial noncoding RNA motif almost exclusively associated with pnuC genes was uncovered using comparative sequence analysis. Some PnuC proteins are known to transport nicotinamide riboside (NR), which is a component of the ubiquitous and abundant enzyme cofactor nicotinamide adenine dinucleotide (NAD+). Thus, we speculated that the newly found “pnuC motif” RNAs might function as aptamers for a novel class of NAD+-sensing riboswitches. RNA constructs that encompass the conserved nucleotides and secondary structure features that define the motif indeed selectively bind NAD+, nicotinamide mononucleotide (NMN), and NR. Mutations that disrupt strictly conserved nucleotides of the aptamer also disrupt ligand binding. These bioinformatic and biochemical findings indicate that pnuC motif RNAs are likely members of a second riboswitch class that regulates gene expression in response to NAD+ binding.

Keywords

Footnotes

  • Received September 23, 2020.
  • Accepted October 19, 2020.

This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.

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