Variants of the guanine riboswitch class exhibit altered ligand specificities for xanthine, guanine, or 2'-deoxyguanosine

Proc Natl Acad Sci U S A. 2022 May 31;119(22):e2120246119. doi: 10.1073/pnas.2120246119. Epub 2022 May 27.

Abstract

The aptamer portions of previously reported riboswitch classes that sense guanine, adenine, or 2′-deoxyguanosine are formed by a highly similar three-stem junction with distinct nucleotide sequences in the regions joining the stems. The nucleotides in these joining regions form the major features of the selective ligand-binding pocket for each aptamer. Previously, we reported the existence of additional, rare variants of the predominant guanine-sensing riboswitch class that carry nucleotide differences in the ligand-binding pocket, suggesting that these RNAs have further diversified their structures and functions. Herein, we report the discovery and analysis of three naturally occurring variants of guanine riboswitches that are narrowly distributed across Firmicutes. These RNAs were identified using comparative sequence analysis methods, which also revealed that some of the gene associations for these variants are atypical for guanine riboswitches or their previously known natural variants. Binding assays demonstrate that the newfound variant riboswitch representatives recognize xanthine, guanine, or 2′-deoxyguanosine, with the guanine class exhibiting greater discrimination against related purines than the more common guanine riboswitch class reported previously. These three additional variant classes, together with the four previously discovered riboswitch classes that employ the same three-stem junction architecture, reveal how a simple structural framework can be diversified to expand the range of purine-based ligands sensed by RNA.

Keywords: aptamer; gene regulation; purine; transcription termination.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Deoxyguanosine* / metabolism
  • Firmicutes* / genetics
  • Firmicutes* / metabolism
  • Guanine* / metabolism
  • Ligands
  • Nucleic Acid Conformation
  • Riboswitch* / genetics
  • Riboswitch* / physiology
  • Xanthine* / metabolism

Substances

  • Ligands
  • Riboswitch
  • Xanthine
  • Guanine
  • Deoxyguanosine