Literature DB >> 11250907

Structure, folding and activity of the VS ribozyme: importance of the 2-3-6 helical junction.

D A Lafontaine1, D G Norman, D M Lilley.   

Abstract

The VS nucleolytic ribozyme has a core comprising five helices organized by two three-way junctions. The ribozyme can act in trans on a hairpin-loop substrate, with which it interacts via tertiary contacts. We have determined that one of the junctions (2-3-6) undergoes two-stage ion-dependent folding into a stable conformation, and have determined the global structure of the folded junction using long-range distance restraints derived from fluorescence resonance energy transfer. A number of sequence variants in the junction are severely impaired in ribozyme cleavage, and there is good correlation between changes in activity and alteration in the folding of junction 2-3-6. These studies point to a special importance of G and A nucleotides immediately adjacent to helix II, and comparison with a similar junction of known structure indicates that this could adopt a guanine-wedge structure. We propose that the 2-3-6 junction organizes important aspects of the structure of the ribozyme to facilitate productive association with the substrate, and suggest that this results in an interaction between the substrate and the A730 loop to create the active complex.

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Year:  2001        PMID: 11250907      PMCID: PMC145516          DOI: 10.1093/emboj/20.6.1415

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  34 in total

1.  The crystal structure of an all-RNA hammerhead ribozyme: a proposed mechanism for RNA catalytic cleavage.

Authors:  W G Scott; J T Finch; A Klug
Journal:  Cell       Date:  1995-06-30       Impact factor: 41.582

2.  Ion-induced folding of the hammerhead ribozyme: a fluorescence resonance energy transfer study.

Authors:  G S Bassi; A I Murchie; F Walter; R M Clegg; D M Lilley
Journal:  EMBO J       Date:  1997-12-15       Impact factor: 11.598

3.  A long-range pseudoknot is required for activity of the Neurospora VS ribozyme.

Authors:  T Rastogi; T L Beattie; J E Olive; R A Collins
Journal:  EMBO J       Date:  1996-06-03       Impact factor: 11.598

4.  Capturing the structure of a catalytic RNA intermediate: the hammerhead ribozyme.

Authors:  W G Scott; J B Murray; J R Arnold; B L Stoddard; A Klug
Journal:  Science       Date:  1996-12-20       Impact factor: 47.728

5.  Identification of functional domains in the self-cleaving Neurospora VS ribozyme using damage selection.

Authors:  T L Beattie; R A Collins
Journal:  J Mol Biol       Date:  1997-04-11       Impact factor: 5.469

6.  Ionic interactions and the global conformations of the hammerhead ribozyme.

Authors:  G S Bassi; N E Møllegaard; A I Murchie; E von Kitzing; D M Lilley
Journal:  Nat Struct Biol       Date:  1995-01

7.  The global folding of four-way helical junctions in RNA, including that in U1 snRNA.

Authors:  D R Duckett; A I Murchie; D M Lilley
Journal:  Cell       Date:  1995-12-15       Impact factor: 41.582

8.  The ion-induced folding of the hammerhead ribozyme: core sequence changes that perturb folding into the active conformation.

Authors:  G S Bassi; A I Murchie; D M Lilley
Journal:  RNA       Date:  1996-08       Impact factor: 4.942

9.  A secondary-structure model for the self-cleaving region of Neurospora VS RNA.

Authors:  T L Beattie; J E Olive; R A Collins
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

10.  Efficient trans-cleavage of a stem-loop RNA substrate by a ribozyme derived from neurospora VS RNA.

Authors:  H C Guo; R A Collins
Journal:  EMBO J       Date:  1995-01-16       Impact factor: 11.598

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  32 in total

1.  Rapid formation of a solvent-inaccessible core in the Neurospora Varkud satellite ribozyme.

Authors:  S L Hiley; R A Collins
Journal:  EMBO J       Date:  2001-10-01       Impact factor: 11.598

Review 2.  Ribozyme speed limits.

Authors:  Gail Mitchell Emilsson; Shingo Nakamura; Adam Roth; Ronald R Breaker
Journal:  RNA       Date:  2003-08       Impact factor: 4.942

3.  The role of phosphate groups in the VS ribozyme-substrate interaction.

Authors:  Yana S Kovacheva; Svetomir B Tzokov; Iain A Murray; Jane A Grasby
Journal:  Nucleic Acids Res       Date:  2004-12-01       Impact factor: 16.971

4.  Topology of three-way junctions in folded RNAs.

Authors:  Aurélie Lescoute; Eric Westhof
Journal:  RNA       Date:  2006-01       Impact factor: 4.942

5.  A loop loop interaction and a K-turn motif located in the lysine aptamer domain are important for the riboswitch gene regulation control.

Authors:  Simon Blouin; Daniel A Lafontaine
Journal:  RNA       Date:  2007-06-21       Impact factor: 4.942

6.  An important role of G638 in the cis-cleavage reaction of the Neurospora VS ribozyme revealed by a novel nucleotide analog incorporation method.

Authors:  Dominic Jaikaran; M Duane Smith; Reza Mehdizadeh; Joan Olive; Richard A Collins
Journal:  RNA       Date:  2008-03-20       Impact factor: 4.942

7.  Constitutive regulatory activity of an evolutionarily excluded riboswitch variant.

Authors:  Renaud Tremblay; Jean-François Lemay; Simon Blouin; Jérôme Mulhbacher; Éric Bonneau; Pascale Legault; Paul Dupont; J Carlos Penedo; Daniel A Lafontaine
Journal:  J Biol Chem       Date:  2011-06-15       Impact factor: 5.157

8.  Structural Basis for Substrate Helix Remodeling and Cleavage Loop Activation in the Varkud Satellite Ribozyme.

Authors:  Saurja DasGupta; Nikolai B Suslov; Joseph A Piccirilli
Journal:  J Am Chem Soc       Date:  2017-07-03       Impact factor: 15.419

9.  Metal-ion-dependent folding of a uranyl-specific DNAzyme: insight into function from fluorescence resonance energy transfer studies.

Authors:  Ying He; Yi Lu
Journal:  Chemistry       Date:  2011-11-03       Impact factor: 5.236

10.  The complete VS ribozyme in solution studied by small-angle X-ray scattering.

Authors:  Jan Lipfert; Jonathan Ouellet; David G Norman; Sebastian Doniach; David M J Lilley
Journal:  Structure       Date:  2008-09-10       Impact factor: 5.006

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