4.7 Article

Global RNA Fold and Molecular Recognition for a pfl Riboswitch Bound to ZMP, a Master Regulator of One-Carbon Metabolism

Journal

STRUCTURE
Volume 23, Issue 8, Pages 1375-1381

Publisher

CELL PRESS
DOI: 10.1016/j.str.2015.05.016

Keywords

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Funding

  1. NIH [U19 CA179564]
  2. National Institute of General Medical Sciences from the NIH [P41 GM103403]
  3. NIH-ORIP HEI grant [S10 RR029205]
  4. DOE Office of Science [DE-AC02-06CH11357]

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ZTP, the pyrophosphorylated analog of ZMP (5amino-4-imidazole carboxamide ribose-50-monophosphate), was identified as an alarmone that senses 10-formyl-tetrahydroflate deficiency in bacteria. Recently, a pfl riboswitch was identified that selectively binds ZMP and regulates genes associated with purine biosynthesis and one-carbon metabolism. We report on the structure of the ZMP-bound Thermosinus carboxydivorans pfl riboswitch sensing domain, thereby defining the pseudoknot-based tertiary RNA fold, the binding-pocket architecture, and principles underlying ligand recognition specificity. Molecular recognition involves shape complementarity, with the ZMP 5-amino and carboxamide groups paired with the Watson-Crick edge of an invariant uracil, and the imidazole ring sandwiched between guanines, while the sugar hydroxyls form intermolecular hydrogen bond contacts. The burial of the ZMP base and ribose moieties, together with unanticipated coordination of the carboxamide by Mg2+, contrasts with exposure of the 50-phosphate to solvent. Our studies highlight the principles underlying RNA-based recognition of ZMP, a master regulator of one-carbon metabolism.

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