Abstract

Nucleobase modifications dramatically alter nucleic acid structure and thermodynamics. 2-thiouridine (s2U) is a modified nucleobase found in tRNAs and known to stabilize U:A base pairs and destabilize U:G wobble pairs. The recently reported crystal structures of s2U-containing RNA duplexes do not entirely explain the mechanisms responsible for the stabilizing effect of s2U or whether this effect is entropic or enthalpic in origin. We present here thermodynamic evaluations of duplex formation using ITC and UV thermal denaturation with RNA duplexes containing internal s2U:A and s2U:U pairs and their native counterparts. These results indicate that s2U stabilizes both duplexes. The stabilizing effect is entropic in origin and likely results from the s2U-induced preorganization of the single-stranded RNA prior to hybridization. The same preorganizing effect is likely responsible for structurally resolving the s2U:U pair-containing duplex into a single conformation with a well-defined H-bond geometry. We also evaluate the effect of s2U on single strand conformation using UV- and CD-monitored thermal denaturation and on nucleoside conformation using 1H NMR spectroscopy, MD and umbrella sampling. These results provide insights into the effects that nucleobase modification has on RNA structure and thermodynamics and inform efforts toward improving both ribozyme-catalyzed and nonenzymatic RNA copying.

Highlights

  • RNA plays an essential and diverse role in living systems, acting as genetic information carrier, catalyst and regulator [1,2,3,4]

  • We evaluated the thermodynamic contributions of structure and thermodynamics. 2-thiouridine (s2U) toward RNA duplex stability by Isothermal titration calorimetry (ITC)

  • A favorable change in enthalpy is associated with both steps: heat is released as the bases stack during the ordering of the single strands; and as H-bonds are formed during duplex formation

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Summary

Introduction

RNA plays an essential and diverse role in living systems, acting as genetic information carrier, catalyst and regulator [1,2,3,4]. Functional RNAs adopt many well-defined 3D structures resulting from specific base–base interactions including normal Watson–Crick base pairs and a variety of other associations [5]. Nucleobase modification diversifies nucleic acid structure and function [7] The significance of this role is reflected by the fact that certain modified nucleobases are among the most highly conserved features of RNA and, for this reason, are regarded as chemical fossils of molecular evolution. Of the approximately 140 known post-transcriptional RNA modifications, 60 are specific to uridine (U) and 16 feature thiolation at the C2 position of U [8]. These modified nucleobases include s2U and various 5-modified derivatives of s2U. Improved codon-anticodon recognition resulting from 2-thiolation in the human tRNALys3UUU has proved to be important for reverse transcription of the HIV-1 viral genome [12]

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