Literature DB >> 2406615

A 3' splice site-binding sequence in the catalytic core of a group I intron.

J M Burke1, J S Esherick, W R Burfeind, J L King.   

Abstract

Ribozymes use specific RNA-RNA interactions for substrate binding and active-site formation. Self-splicing group I introns have approximately 70 nucleotides constituting the core, a region containing sequences and structures indispensable for catalytic function. The catalytic core must interact with the substrates used for the two steps of the self-splicing reaction, that is, guanosine, the 5'-splice-site helix (P1) and the 3' splice site. Mutational evidence suggests that core sequences near segment J6/7 that joins the base-paired stems P6 and P7, and the bulged base of P7(5'), participate in binding guanosine substrate, but nothing is known about the interactions between the core, the 5'-splice-site helix and the 3' splice site. On the basis of comparative sequence data, it has been suggested that two specific bases in the catalytic core of group I introns might form a binding sequence for the 3' splice site. Here we present genetic evidence that such a binding site exists in the core of the Tetrahymena large subunit ribosomal RNA intron. We demonstrate that this pairing, termed P9.0, is functionally important in the exon ligation step of self-splicing, but is not itself responsible for 3'-splice-site selection.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2406615     DOI: 10.1038/344080a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  20 in total

1.  In vivo excision of a single targeted nucleotide from an mRNA by a trans excision-splicing ribozyme.

Authors:  Dana A Baum; Stephen M Testa
Journal:  RNA       Date:  2005-05-04       Impact factor: 4.942

2.  Yeast transcripts cleaved by an internal ribozyme provide new insight into the role of the cap and poly(A) tail in translation and mRNA decay.

Authors:  Stacie Meaux; Ambro Van Hoof
Journal:  RNA       Date:  2006-05-19       Impact factor: 4.942

3.  The Cbp2 protein suppresses splice site mutations in a group I intron.

Authors:  L C Shaw; J Thomas; A S Lewin
Journal:  Nucleic Acids Res       Date:  1996-09-01       Impact factor: 16.971

4.  A small insertion in the SSU rDNA of the lichen fungus Arthonia lapidicola is a degenerate group-I intron.

Authors:  M Grube; A Gargas; P T DePriest
Journal:  Curr Genet       Date:  1996-05       Impact factor: 3.886

5.  The site-specific DNA endonuclease encoded by a group I intron in the Chlamydomonas pallidostigmatica chloroplast small subunit rRNA gene introduces a single-strand break at low concentrations of Mg2+.

Authors:  M Turmel; J P Mercier; V Côté; C Otis; C Lemieux
Journal:  Nucleic Acids Res       Date:  1995-07-11       Impact factor: 16.971

6.  Cooperative and anticooperative binding to a ribozyme.

Authors:  P C Bevilacqua; K A Johnson; D H Turner
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-15       Impact factor: 11.205

7.  Novel system for analysis of group I 3' splice site reactions based on functional trans-interaction of the P1/P10 reaction helix with the ribozyme's catalytic core.

Authors:  B M Chowrira; A Berzal-Herranz; J M Burke
Journal:  Nucleic Acids Res       Date:  1995-03-11       Impact factor: 16.971

8.  Interlocked circle formation by group I introns: structural requirements and mechanism.

Authors:  A J Winter; M J Alkema; M J Groot Koerkamp; G van der Horst; Y Mul; H F Tabak
Journal:  Nucleic Acids Res       Date:  1993-07-11       Impact factor: 16.971

9.  Group I introns interrupt the chloroplast psaB and psbC and the mitochondrial rrnL gene in Chlamydomonas.

Authors:  M Turmel; J P Mercier; M J Côté
Journal:  Nucleic Acids Res       Date:  1993-11-11       Impact factor: 16.971

10.  Splice site selection by intron aI3 of the COX1 gene from Saccharomyces cerevisiae.

Authors:  A J Winter; M J Groot Koerkamp; H F Tabak
Journal:  Nucleic Acids Res       Date:  1992-08-11       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.