Literature DB >> 7720718

Frequent use of the same tertiary motif by self-folding RNAs.

M Costa1, F Michel.   

Abstract

We have identified an 11 nucleotide RNA motif, [CCUAAG...UAUGG], that is extraordinarily abundant in group I and group II self-splicing introns at sites known, or suspected from co-variation analysis, to interact with hairpin terminal loops with a GNRA consensus sequence. Base substitution experiments using a ribozyme-substrate system derived from a group I intron reveal that this motif interacts preferentially with GAAA terminal loops and binds them with remarkable affinity, compared with other known combinations of GNRA loops and matched targets. A copy of the [CCUAAG...UAUGG] motif which is present in domain I of many group II introns is shown to interact with the GAAA terminal loop that caps domain V. This is the first interaction to be identified between these two domains, whose mutual recognition is known to be necessary and sufficient for group II ribozymic activity. We conclude that interaction of [CCUAAG...UAUGG] with GAAA loops is one of the most common solutions used by nature to solve the problem of compacting and bringing together RNA structural domains.

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Year:  1995        PMID: 7720718      PMCID: PMC398207          DOI: 10.1002/j.1460-2075.1995.tb07111.x

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


  39 in total

1.  Context dependence of hydrogen bond free energy revealed by substitutions in an RNA hairpin.

Authors:  J SantaLucia; R Kierzek; D H Turner
Journal:  Science       Date:  1992-04-10       Impact factor: 47.728

2.  Group II introns deleted for multiple substructures retain self-splicing activity.

Authors:  J L Koch; S C Boulanger; S D Dib-Hajj; S K Hebbar; P S Perlman
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

3.  Activation of the catalytic core of a group I intron by a remote 3' splice junction.

Authors:  F Michel; L Jaeger; E Westhof; R Kuras; F Tihy; M Q Xu; D A Shub
Journal:  Genes Dev       Date:  1992-08       Impact factor: 11.361

4.  The conformation of the sarcin/ricin loop from 28S ribosomal RNA.

Authors:  A A Szewczak; P B Moore; Y L Chang; I G Wool
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

5.  Crystallization of ribozymes and small RNA motifs by a sparse matrix approach.

Authors:  J A Doudna; C Grosshans; A Gooding; C E Kundrot
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-15       Impact factor: 11.205

6.  Monitoring of the cooperative unfolding of the sunY group I intron of bacteriophage T4. The active form of the sunY ribozyme is stabilized by multiple interactions with 3' terminal intron components.

Authors:  L Jaeger; E Westhof; F Michel
Journal:  J Mol Biol       Date:  1993-11-20       Impact factor: 5.469

7.  An independently folding domain of RNA tertiary structure within the Tetrahymena ribozyme.

Authors:  F L Murphy; T R Cech
Journal:  Biochemistry       Date:  1993-05-25       Impact factor: 3.162

8.  Replacement of RNA hairpins by in vitro selected tetranucleotides.

Authors:  B Dichtl; T Pan; A B DiRenzo; O C Uhlenbeck
Journal:  Nucleic Acids Res       Date:  1993-02-11       Impact factor: 16.971

9.  Dynamics of ribozyme binding of substrate revealed by fluorescence-detected stopped-flow methods.

Authors:  P C Bevilacqua; R Kierzek; K A Johnson; D H Turner
Journal:  Science       Date:  1992-11-20       Impact factor: 47.728

10.  Interaction of intronic boundaries is required for the second splicing step efficiency of a group II intron.

Authors:  G Chanfreau; A Jacquier
Journal:  EMBO J       Date:  1993-12-15       Impact factor: 11.598

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  136 in total

1.  In vitro selection of RNAs with increased tertiary structure stability.

Authors:  K Juneau; T R Cech
Journal:  RNA       Date:  1999-08       Impact factor: 4.942

2.  A selection system for functional internal ribosome entry site (IRES) elements: analysis of the requirement for a conserved GNRA tetraloop in the encephalomyocarditis virus IRES.

Authors:  M E Robertson; R A Seamons; G J Belsham
Journal:  RNA       Date:  1999-09       Impact factor: 4.942

3.  TectoRNA: modular assembly units for the construction of RNA nano-objects.

Authors:  L Jaeger; E Westhof; N B Leontis
Journal:  Nucleic Acids Res       Date:  2001-01-15       Impact factor: 16.971

4.  Visualizing the solvent-inaccessible core of a group II intron ribozyme.

Authors:  J Swisher; C M Duarte; L J Su; A M Pyle
Journal:  EMBO J       Date:  2001-04-17       Impact factor: 11.598

5.  Phylogenetic analysis of tmRNA genes within a bacterial subgroup reveals a specific structural signature.

Authors:  B Felden; C Massire; E Westhof; J F Atkins; R F Gesteland
Journal:  Nucleic Acids Res       Date:  2001-04-01       Impact factor: 16.971

6.  Influence of specific mutations on the thermal stability of the td group I intron in vitro and on its splicing efficiency in vivo: a comparative study.

Authors:  P Brion; R Schroeder; F Michel; E Westhof
Journal:  RNA       Date:  1999-07       Impact factor: 4.942

7.  A complex ligase ribozyme evolved in vitro from a group I ribozyme domain.

Authors:  L Jaeger; M C Wright; G F Joyce
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

8.  Tight binding of the 5' exon to domain I of a group II self-splicing intron requires completion of the intron active site.

Authors:  M Costa; F Michel
Journal:  EMBO J       Date:  1999-02-15       Impact factor: 11.598

Review 9.  Coupled nucleotide covariations reveal dynamic RNA interaction patterns.

Authors:  A P Gultyaev; T Franch; K Gerdes
Journal:  RNA       Date:  2000-11       Impact factor: 4.942

10.  Recruitment of intron-encoded and co-opted proteins in splicing of the bI3 group I intron RNA.

Authors:  Gurminder S Bassi; Daniela M de Oliveira; Malcolm F White; Kevin M Weeks
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-02       Impact factor: 11.205

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