Literature DB >> 3160483

Stepwise assembly of a pre-mRNA splicing complex requires U-snRNPs and specific intron sequences.

D Frendewey, W Keller.   

Abstract

We have investigated the early events of pre-mRNA splicing in vitro by sucrose gradient sedimentation analysis. Time course experiments revealed the assembly, in two steps, of a large (50S) pre-mRNA splicing complex, preceded by formation of two other complexes that sediment at approximately 22S and 35S. Pre-mRNA and the intermediates and products of the in vitro splicing reaction cosediment with the 50S complex, while only pre-mRNA is associated with the 22S and 35S complexes. No splicing is observed in the absence of a 50S complex. Formation of the 50S complex requires ATP, whereas formation of the 22S and 35S complexes does not. U-snRNPs are necessary for assembly of the 35S and the 50S complexes but not for assembly of the 22S complex. Analysis with mutant substrate RNAs demonstrated that a polypyrimidine stretch near the 3' splice site and an intact 5' splice site are absolutely required for splicing complex formation.

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Year:  1985        PMID: 3160483     DOI: 10.1016/s0092-8674(85)80131-8

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


  224 in total

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Authors:  C A Collins; C Guthrie
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5.  cis-acting sequences involved in exon selection in the chicken beta-tropomyosin gene.

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7.  The spliceosome assembly pathway in mammalian extracts.

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

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9.  Model for tissue specific Calcitonin/CGRP-I RNA processing from in vitro experiments.

Authors:  R A Bovenberg; G J Adema; H S Jansz; P D Baas
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10.  Unusual branch point selection involved in splicing of the alternatively processed Calcitonin/CGRP-I pre-mRNA.

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