Literature DB >> 10889027

Impact of phosphorothioate substitutions on the thermodynamic stability of an RNA GAAA tetraloop: an unexpected stabilization.

T E Horton1, M Maderia, V J DeRose.   

Abstract

This study analyzes the impact of phosphorothioate substitutions on the thermodynamic stability of a 12-nt RNA hairpin containing a (5')GAAA(3') tetraloop. The thermodynamic consequences of stereospecific phosphorothioate substitutions 5' to each adenosine in the loop region are measured using optical melting and calorimetry experiments. Surprisingly, a single stereospecific phosphorothioate substitution 5' to the second adenosine of the tetraloop, R(p)-A7, results in a stabilization corresponding to a Delta(DeltaG(37)(degrees)(C)) of approximately -2.9 kcal mol(-1) (0.1 M NaCl) when compared with that of an unmodified sample. Five other phosphorothioate-substituted samples did not show significant thermodynamic differences in comparison with the unsubstituted samples. Addition of Mg(2+) to all of the hairpins studied results in increased t(m's) that are fit with a general electrostatic model to a dissociation constant of K(d)(Mg(2+)) approximately 2-3 mM (0.1 M NaCl). The R(p)-A7 phosphorothioate-substituted hairpin showed an unusual decrease in t(m) and apparent increase in enthalpy of unfolding upon addition of Cd(2+). These results may impact the interpretation of interference mapping experiments that use phosphorothioate substitutions to characterize RNAs in solution.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10889027     DOI: 10.1021/bi000141d

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  7 in total

1.  Common and distinctive features of GNRA tetraloops based on a GUAA tetraloop structure at 1.4 A resolution.

Authors:  Carl C Correll; Kerren Swinger
Journal:  RNA       Date:  2003-03       Impact factor: 4.942

2.  Distinct sites of phosphorothioate substitution interfere with folding and splicing of the Anabaena group I intron.

Authors:  Andrej Lupták; Jennifer A Doudna
Journal:  Nucleic Acids Res       Date:  2004-04-23       Impact factor: 16.971

3.  Specific metal-ion binding sites in a model of the P4-P6 triple-helical domain of a group I intron.

Authors:  M Lindqvist; K Sandström; V Liepins; R Strömberg; A Gräslund
Journal:  RNA       Date:  2001-08       Impact factor: 4.942

4.  Specific phosphorothioate substitutions probe the active site of Bacillus subtilis ribonuclease P.

Authors:  Sharon M Crary; Jeffrey C Kurz; Carol A Fierke
Journal:  RNA       Date:  2002-07       Impact factor: 4.942

5.  Recruitment of divalent metal ions by incorporation of 4-thio-2'-deoxythymidine or 4-thio-2'-deoxyuridine into DNA.

Authors:  Olga Iranzo; Homayoon Khalili; Daniel M Epstein; Janet R Morrow
Journal:  J Biol Inorg Chem       Date:  2004-04-30       Impact factor: 3.358

6.  Multiple metal-binding cores are required for metalloregulation by M-box riboswitch RNAs.

Authors:  Catherine A Wakeman; Arati Ramesh; Wade C Winkler
Journal:  J Mol Biol       Date:  2009-07-17       Impact factor: 5.469

7.  NMR localization of divalent cations at the active site of the Neurospora VS ribozyme provides insights into RNA-metal-ion interactions.

Authors:  Eric Bonneau; Pascale Legault
Journal:  Biochemistry       Date:  2014-01-10       Impact factor: 3.162

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.