Mg2+∈modulation of EMCV IRES key activity fragment equilibria and r(G•C) base-pair kinetics

J. A. Dupont, K. Snoussi

Research output: Contribution to journalArticle

Abstract

NMR magnetization transfer from water and ammonia-catalyzed exchange of the imino proton have been used to probe enhanced thermostability and conformational rearrangements induced by Mg2∈+∈ in two key activity fragments r(CACCUGGCGACAGGUG) and r(GGCCAAAAGCC) of the encephalomyocarditis virus (EMCV) picornavirus internal ribosome entry site (IRES). We have measured some of their r(G•C) base-pair lifetimes and dissociation constants under different MgCl2 conditions, and we compare them with those of other short RNA duplexes. The RNA fragment r(CACCUGGCGACAGGUG) adopts two topologies, a palindromic duplex with two conformations and a hairpin, whose equilibrium can be monitored: the duplex form is destabilized by Mg2∈+∈ and temperature, a delicate balance wherein the entropic contribution of the free energy helps populate the hairpin state. For both fragments, the opening rates of the r(G•C) pairs are lower in the presence of Mg2∈+∈ and their dissociation constants are smaller or comparable. Analysis of the results suggests that Mg2∈+∈ has a preferential and specific effect on the r(CACCUGGCGACAGGUG) hairpin in the region close to the r(G•C) closing pair of the GCGA tetraloop, and the ion moves diffusively around r(GGCCAAAAGCC), thereby differentiating the GNRA and RAAA hairpin motifs that are both involved in the biological regulation functions of the EMCV IRES.

Original languageEnglish (US)
Pages (from-to)231-243
Number of pages13
JournalJournal of Biological Physics
Volume35
Issue number3
DOIs
Publication statusPublished - Aug 2009
Externally publishedYes

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Keywords

  • Base-pair kinetics
  • EMCV IRES
  • GNRA tetraloop
  • Imino proton exchange
  • Mg2+
  • NMR
  • RAAA hairpin motif

ASJC Scopus subject areas

  • Biophysics
  • Cell Biology
  • Molecular Biology
  • Atomic and Molecular Physics, and Optics

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