Literature DB >> 7489486

Self-assembly of a group I intron active site from its component tertiary structural domains.

J A Doudna1, T R Cech.   

Abstract

The catalytic core of Group I self-splicing introns has been proposed to consist of two structural domains, P4-P6 and P3-P9. Each contains helical segments and conserved unpaired nucleotides, and the isolated P4-P6 domain has been shown to have substantial native tertiary structure. The proposed tertiary structure domains of the Tetrahymena intron were synthesized separately and shown to self-assemble into a catalytically active complex. Surprisingly, the concentration dependence of these reactions revealed that the domains interact with nanomolar apparent dissociation constants, even though there is no known base pairing between P4-P6 and P3-P9. This suggests that the domains interact through multiple tertiary contacts, the nature of which can now be explored in this system. For example, a circularly permuted version of the P4-P6 domain, which folds similarly to the native P4-P6 molecule, formed a stable but inactive complex. Interestingly, activity was demonstrated with the permuted molecule when nucleotides proposed to form a triple-strand interaction with P4 and P6 were restored as part of the P1-P3 substrate or as part of the P3-P9 RNA. Thus, beyond stabilization of the P4-P6 domain, the triple-strand region may facilitate correct orientation of the RNA domains or participate more directly in catalysis.

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Year:  1995        PMID: 7489486      PMCID: PMC1369057     

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  24 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.  Two inactive fragments of the integral RNA cooperate to assemble active telomerase with the human protein catalytic subunit (hTERT) in vitro.

Authors:  V M Tesmer; L P Ford; S E Holt; B C Frank; X Yi; D L Aisner; M Ouellette; J W Shay; W E Wright
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

3.  Quantifying the energetic interplay of RNA tertiary and secondary structure interactions.

Authors:  S K Silverman; M Zheng; M Wu; I Tinoco; T R Cech
Journal:  RNA       Date:  1999-12       Impact factor: 4.942

4.  A hierarchy of RNA subdomains in assembly of the central domain of the 30 S ribosomal subunit.

Authors:  S C Agalarov; J R Williamson
Journal:  RNA       Date:  2000-03       Impact factor: 4.942

5.  De novo synthesis and development of an RNA enzyme.

Authors:  Yoshiya Ikawa; Kentaro Tsuda; Shigeyoshi Matsumura; Tan Inoue
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-13       Impact factor: 11.205

6.  Communication between RNA folding domains revealed by folding of circularly permuted ribozymes.

Authors:  Richard A Lease; Tadepalli Adilakshmi; Susan Heilman-Miller; Sarah A Woodson
Journal:  J Mol Biol       Date:  2007-07-12       Impact factor: 5.469

7.  Toward predicting self-splicing and protein-facilitated splicing of group I introns.

Authors:  Quentin Vicens; Paul J Paukstelis; Eric Westhof; Alan M Lambowitz; Thomas R Cech
Journal:  RNA       Date:  2008-09-03       Impact factor: 4.942

8.  A map of the binding site for catalytic domain 5 in the core of a group II intron ribozyme.

Authors:  B B Konforti; Q Liu; A M Pyle
Journal:  EMBO J       Date:  1998-12-01       Impact factor: 11.598

9.  Multiple substrate binding sites in the ribozyme from Bacillus subtilis RNase P.

Authors:  T Pan; M Jakacka
Journal:  EMBO J       Date:  1996-05-01       Impact factor: 11.598

10.  Oligonucleotide directed misfolding of RNA inhibits Candida albicans group I intron splicing.

Authors:  Jessica L Childs; Matthew D Disney; Douglas H Turner
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-08       Impact factor: 11.205

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