Literature DB >> 3552247

Recognition of the TACTAAC box during mRNA splicing in yeast involves base pairing to the U2-like snRNA.

R Parker, P G Siliciano, C Guthrie.   

Abstract

The U2 snRNP binds to the site of branch formation during splicing of mammalian pre-mRNA in vitro. In Saccharomyces cerevisiae the branch site is within the so-called TACTAAC box (UACUAAC box), an absolutely conserved intron sequence required for splicing. Based on the identification and sequence of a U2 analogue in yeast, a specific base pairing interaction between the UACUAAC box and a highly conserved region of this snRNA can be proposed. To test this hypothesis, we have taken advantage of two mutations constructed previously in the UACUAAC box of an actin-HIS4 fusion. These mutant strains were transformed with stable plasmids bearing U2-like snRNAs into which changes predicted to restore base pairing had been introduced. Allele-specific suppression of biological and biochemical phenotypes was observed in both cases. Recognition of the UACUAAC box thus relies, at least in part, on Watson-Crick base pairing with the yeast U2 analogue.

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Year:  1987        PMID: 3552247     DOI: 10.1016/0092-8674(87)90564-2

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  210 in total

1.  A splice site mutant of maize activates cryptic splice sites, elicits intron inclusion and exon exclusion, and permits branch point elucidation.

Authors:  S Lal; J H Choi; J R Shaw; L C Hannah
Journal:  Plant Physiol       Date:  1999-10       Impact factor: 8.340

2.  Sequences upstream of the branch site are required to form helix II between U2 and U6 snRNA in a trans-splicing reaction.

Authors:  G Ast; T Pavelitz; A M Weiner
Journal:  Nucleic Acids Res       Date:  2001-04-15       Impact factor: 16.971

3.  Splicing enhancement in the yeast rp51b intron.

Authors:  D Libri; A Lescure; M Rosbash
Journal:  RNA       Date:  2000-03       Impact factor: 4.942

4.  Evolutionary conservation of post-transcriptional 3' end adenylation of small RNAs: S. cerevisiae signal recognition particle RNA and U2 small nuclear RNA are post-transcriptionally adenylated.

Authors:  K Perumal; J Gu; R Reddy
Journal:  Mol Cell Biochem       Date:  2000-05       Impact factor: 3.396

5.  ATP-dependent interaction of yeast U5 snRNA loop 1 with the 5' splice site.

Authors:  R K Alvi; M Lund; R T Okeefe
Journal:  RNA       Date:  2001-07       Impact factor: 4.942

6.  The ATP requirement for U2 snRNP addition is linked to the pre-mRNA region 5' to the branch site.

Authors:  C M Newnham; C C Query
Journal:  RNA       Date:  2001-09       Impact factor: 4.942

7.  Crystal structure of a model branchpoint-U2 snRNA duplex containing bulged adenosines.

Authors:  J A Berglund; M Rosbash; S C Schultz
Journal:  RNA       Date:  2001-05       Impact factor: 4.942

8.  Unusual branch point selection involved in splicing of the alternatively processed Calcitonin/CGRP-I pre-mRNA.

Authors:  G J Adema; R A Bovenberg; H S Jansz; P D Baas
Journal:  Nucleic Acids Res       Date:  1988-10-25       Impact factor: 16.971

9.  Oligonucleotide-targeted degradation of U1 and U2 snRNAs reveals differential interactions of simian virus 40 pre-mRNAs with snRNPs.

Authors:  Z Q Pan; H Ge; X Y Fu; J L Manley; C Prives
Journal:  Nucleic Acids Res       Date:  1989-08-25       Impact factor: 16.971

10.  UACUAAC is the preferred branch site for mammalian mRNA splicing.

Authors:  Y A Zhuang; A M Goldstein; A M Weiner
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

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