Literature DB >> 3286372

A chemical modification/interference study of yeast pre-mRNA spliceosome assembly and splicing.

B C Rymond1, M Rosbash.   

Abstract

A chemical modification/interference assay was used to determine the yeast pre-mRNA sequence requirements for in vitro spliceosome assembly and splicing. Modifications of any of the nucleotides within the 5' splice site and branch point (TACTAAC box) consensus sequences as well as less conserved intron and exon positions were found to inhibit assembly and/or splicing. The interference pattern of the 5' splice site and TACTAAC box lesions increased as spliceosome assembly proceeded (complex III----complex I----complex II) and as splicing proceeded, suggesting that these sequence elements play multiple roles in the assembly of yeast spliceosomes and in the removal of intervening sequences. Furthermore, modification (or mutation) of a TACTAAC-like sequence upstream of the branch point was found to inhibit the rate of spliceosome assembly, implying a possible role for degenerate branch point sequences in modulating the efficiency of spliceosome assembly.

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Year:  1988        PMID: 3286372     DOI: 10.1101/gad.2.4.428

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  18 in total

1.  Differential recognition of the polypyrimidine-tract by the general splicing factor U2AF65 and the splicing repressor sex-lethal.

Authors:  R Singh; H Banerjee; M R Green
Journal:  RNA       Date:  2000-06       Impact factor: 4.942

2.  Requirements for U2 snRNP addition to yeast pre-mRNA.

Authors:  X C Liao; H V Colot; Y Wang; M Rosbash
Journal:  Nucleic Acids Res       Date:  1992-08-25       Impact factor: 16.971

3.  Domain structure of U2 and U4/U6 small nuclear ribonucleoprotein particles from Trypanosoma brucei: identification of trans-spliceosomal specific RNA-protein interactions.

Authors:  A Günzl; M Cross; A Bindereif
Journal:  Mol Cell Biol       Date:  1992-02       Impact factor: 4.272

4.  Sequence requirements in different steps of the pre-mRNA splicing reaction: analysis by the RNA modification-exclusion technique.

Authors:  K M Lang; W Keller
Journal:  Mol Cell Biol       Date:  1990-09       Impact factor: 4.272

5.  Sequence requirements for branch formation in a group II self-splicing intron.

Authors:  R Altura; B Rymond; B Seraphin; M Rosbash
Journal:  Nucleic Acids Res       Date:  1989-01-11       Impact factor: 16.971

Review 6.  RNA nanotechnology: engineering, assembly and applications in detection, gene delivery and therapy.

Authors:  Peixuan Guo
Journal:  J Nanosci Nanotechnol       Date:  2005-12

7.  Phosphorothioate substitution identifies phosphate groups important for pre-mRNA splicing.

Authors:  K L Maschhoff; R A Padgett
Journal:  Nucleic Acids Res       Date:  1992-04-25       Impact factor: 16.971

8.  Progression through the spliceosome cycle requires Prp38p function for U4/U6 snRNA dissociation.

Authors:  J Xie; K Beickman; E Otte; B C Rymond
Journal:  EMBO J       Date:  1998-05-15       Impact factor: 11.598

9.  Identification and characterization of a yeast homolog of U1 snRNP-specific protein C.

Authors:  J Tang; N Abovich; M L Fleming; B Seraphin; M Rosbash
Journal:  EMBO J       Date:  1997-07-01       Impact factor: 11.598

10.  Commitment of yeast pre-mRNA to the splicing pathway requires a novel U1 small nuclear ribonucleoprotein polypeptide, Prp39p.

Authors:  S R Lockhart; B C Rymond
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

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