Literature DB >> 16483935

Repositioning of the reaction intermediate within the catalytic center of the spliceosome.

Maria M Konarska1, Josep Vilardell, Charles C Query.   

Abstract

Conformational change within the spliceosome is required between the first catalytic step of pre-mRNA splicing, when the branch site attacks the 5' splice site (SS), and the second step, when the 5' exon attacks the 3'SS. Little is known, however, about repositioning of the reaction substrates during this transition. Whereas the 5'SS is positioned for the first step by pairing with the invariant U6 snRNA-ACAGAG site, we demonstrate that this pairing interaction must be disrupted to allow transition to the second step. We propose that removal of the branch structure from the catalytic center is in competition with binding of the 3'SS substrate for the second step. Changes in the relative occupancy of first and second step substrates at the catalytic center alter efficiency of the two steps of splicing, allowing use of suboptimal intron sequences and thereby altering substrate selectivity.

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Substances:

Year:  2006        PMID: 16483935     DOI: 10.1016/j.molcel.2006.01.017

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  63 in total

1.  CEF1/CDC5 alleles modulate transitions between catalytic conformations of the spliceosome.

Authors:  Charles C Query; Maria M Konarska
Journal:  RNA       Date:  2012-03-08       Impact factor: 4.942

2.  Structure of the yeast U2/U6 snRNA complex.

Authors:  Jordan E Burke; Dipali G Sashital; Xiaobing Zuo; Yun-Xing Wang; Samuel E Butcher
Journal:  RNA       Date:  2012-02-10       Impact factor: 4.942

3.  RPL30 regulation of splicing reveals distinct roles for Cbp80 in U1 and U2 snRNP cotranscriptional recruitment.

Authors:  Mireia Bragulat; Markus Meyer; Sara Macías; Maria Camats; Mireia Labrador; Josep Vilardell
Journal:  RNA       Date:  2010-08-27       Impact factor: 4.942

Review 4.  Roles of DEAD-box proteins in RNA and RNP Folding.

Authors:  Cynthia Pan; Rick Russell
Journal:  RNA Biol       Date:  2010-11-01       Impact factor: 4.652

5.  Genomic mRNA profiling reveals compensatory mechanisms for the requirement of the essential splicing factor U2AF.

Authors:  Vinod Sridharan; Joseph Heimiller; Ravinder Singh
Journal:  Mol Cell Biol       Date:  2010-12-13       Impact factor: 4.272

6.  Proximity of conserved U6 and U2 snRNA elements to the 5' splice site region in activated spliceosomes.

Authors:  Britta M Rhode; Klaus Hartmuth; Eric Westhof; Reinhard Lührmann
Journal:  EMBO J       Date:  2006-05-11       Impact factor: 11.598

7.  Genomic splice-site analysis reveals frequent alternative splicing close to the dominant splice site.

Authors:  Yimeng Dou; Kristi L Fox-Walsh; Pierre F Baldi; Klemens J Hertel
Journal:  RNA       Date:  2006-10-19       Impact factor: 4.942

8.  Rearrangement of competing U2 RNA helices within the spliceosome promotes multiple steps in splicing.

Authors:  Rhonda J Perriman; Manuel Ares
Journal:  Genes Dev       Date:  2007-04-01       Impact factor: 11.361

9.  trans-splicing to spliceosomal U2 snRNA suggests disruption of branch site-U2 pairing during pre-mRNA splicing.

Authors:  Duncan J Smith; Charles C Query; Maria M Konarska
Journal:  Mol Cell       Date:  2007-06-22       Impact factor: 17.970

10.  A large intrinsically disordered region in SKIP and its disorder-order transition induced by PPIL1 binding revealed by NMR.

Authors:  Xingsheng Wang; Shaojie Zhang; Jiahai Zhang; Xiaojuan Huang; Chao Xu; Weiwei Wang; Zhijun Liu; Jihui Wu; Yunyu Shi
Journal:  J Biol Chem       Date:  2009-12-09       Impact factor: 5.157

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