Literature DB >> 1279677

A region of group I introns that contains universally conserved residues but is not essential for self-splicing.

K P Williams1, D N Fujimoto, T Inoue.   

Abstract

The catalytic core of the self-splicing group I intron RNAs is composed of six paired regions together with their connecting sequences; these are thought to form two elongated domains, with paired regions P5, P4, and P6 aligned along one axis and P8, P3, and P7 along the other. Most of the very highly conserved residues of the group I introns lie in or near P7, but two occur in L4, the internal loop connecting P4 and P5. It is generally believed that such bases are conserved because they are essential for splicing. Mutants were created in a member of each of the two major subclasses of group I introns, in which P5, L4, and the distal portion of P4 were deleted. Splicing activity was still detected in these mutants, albeit substantially weakened; splicing was accurate and occurred by the normal group I mechanism, with addition of a guanosine molecule to the intron. Thus the deleted region, containing two universally conserved bases, is not essential but facilitates splicing. Another reaction characteristic of group I introns, hydrolysis of the 3' splice site, was less severely affected by the deletions. The results are discussed in terms of the prevailing three-dimensional model for the core structure of the group I introns.

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Year:  1992        PMID: 1279677      PMCID: PMC50346          DOI: 10.1073/pnas.89.21.10400

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  25 in total

1.  Phylogenetic and genetic evidence for base-triples in the catalytic domain of group I introns.

Authors:  F Michel; A D Ellington; S Couture; J W Szostak
Journal:  Nature       Date:  1990-10-11       Impact factor: 49.962

2.  RNA-catalysed synthesis of complementary-strand RNA.

Authors:  J A Doudna; J W Szostak
Journal:  Nature       Date:  1989-06-15       Impact factor: 49.962

Review 3.  Comparative and functional anatomy of group II catalytic introns--a review.

Authors:  F Michel; K Umesono; H Ozeki
Journal:  Gene       Date:  1989-10-15       Impact factor: 3.688

4.  Mutational analysis of conserved nucleotides in a self-splicing group I intron.

Authors:  S Couture; A D Ellington; A S Gerber; J M Cherry; J A Doudna; R Green; M Hanna; U Pace; J Rajagopal; J W Szostak
Journal:  J Mol Biol       Date:  1990-10-05       Impact factor: 5.469

5.  A thermodynamic study of unusually stable RNA and DNA hairpins.

Authors:  V P Antao; S Y Lai; I Tinoco
Journal:  Nucleic Acids Res       Date:  1991-11-11       Impact factor: 16.971

6.  U5 snRNA interacts with exon sequences at 5' and 3' splice sites.

Authors:  A J Newman; C Norman
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

7.  Deletion-tolerance and trans-splicing of the bacteriophage T4 td intron. Analysis of the P6-L6a region.

Authors:  J L Galloway Salvo; T Coetzee; M Belfort
Journal:  J Mol Biol       Date:  1990-02-05       Impact factor: 5.469

8.  Splicing of messenger RNA precursors.

Authors:  P A Sharp
Journal:  Science       Date:  1987-02-13       Impact factor: 47.728

9.  Activation of a cryptic 5' splice site in the upstream exon of the phage T4 td transcript: exon context, missplicing, and mRNA deletion in a fidelity mutant.

Authors:  P S Chandry; M Belfort
Journal:  Genes Dev       Date:  1987-11       Impact factor: 11.361

10.  New reactions of the ribosomal RNA precursor of Tetrahymena and the mechanism of self-splicing.

Authors:  T Inoue; F X Sullivan; T R Cech
Journal:  J Mol Biol       Date:  1986-05-05       Impact factor: 5.469

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  6 in total

1.  P5abc of the Tetrahymena ribozyme consists of three functionally independent elements.

Authors:  Y Naito; H Shiraishi; T Inoue
Journal:  RNA       Date:  1998-07       Impact factor: 4.942

2.  Quantitative studies of Mn(2+)-promoted specific and non-specific cleavages of a large RNA: Mn(2+)-GAAA ribozymes and the evolution of small ribozymes.

Authors:  T C Kuo; D L Herrin
Journal:  Nucleic Acids Res       Date:  2000-11-01       Impact factor: 16.971

3.  Methylation interference experiments identify bases that are essential for distinct catalytic functions of a group I ribozyme.

Authors:  U von Ahsen; H F Noller
Journal:  EMBO J       Date:  1993-12       Impact factor: 11.598

4.  Two group I ribozymes with different functions in a nuclear rDNA intron.

Authors:  W A Decatur; C Einvik; S Johansen; V M Vogt
Journal:  EMBO J       Date:  1995-09-15       Impact factor: 11.598

5.  Site-specific isotope labeling of long RNA for structural and mechanistic studies.

Authors:  Ikumi Kawahara; Kaichiro Haruta; Yuta Ashihara; Daichi Yamanaka; Mituhiro Kuriyama; Naoko Toki; Yoshinori Kondo; Kenta Teruya; Junya Ishikawa; Hiroyuki Furuta; Yoshiya Ikawa; Chojiro Kojima; Yoshiyuki Tanaka
Journal:  Nucleic Acids Res       Date:  2011-11-12       Impact factor: 16.971

6.  Use of a Fluorescent Aptamer RNA as an Exonic Sequence to Analyze Self-Splicing Ability of aGroup I Intron from Structured RNAs.

Authors:  Airi Furukawa; Takahiro Tanaka; Hiroyuki Furuta; Shigeyoshi Matsumura; Yoshiya Ikawa
Journal:  Biology (Basel)       Date:  2016-11-17
  6 in total

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