Literature DB >> 10640279

ATP can be dispensable for prespliceosome formation in yeast.

R Perriman1, M Ares.   

Abstract

The first ATP-dependent step in pre-mRNA splicing involves the stable binding of U2 snRNP to form the prespliceosome. We show that a prespliceosome-like complex forms in the absence of ATP in yeast extracts lacking the U2 suppressor protein CUS2. These complexes display the same pre-mRNA and U snRNA requirements as authentic prespliceosomes and can be chased through the splicing pathway, indicating that they are a functional intermediate in the spliceosome assembly pathway. ATP-independent prespliceosome-like complexes are also observed in extracts containing a mutant U2 snRNA. Loss of CUS2 does not bypass the role of PRP5, an RNA helicase family member required for ATP-dependent prespliceosome formation. Genetic interactions between CUS2 and a heat-sensitive prp5 allele parallel those observed between CUS2 and U2, and suggest that CUS2 mediates functional interactions between U2 RNA and PRP5. We propose that CUS2 enforces ATP dependence during formation of the prespliceosome by brokering an interaction between PRP5 and the U2 snRNP that depends on correct U2 RNA structure.

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Year:  2000        PMID: 10640279      PMCID: PMC316341     

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


  47 in total

1.  Initial recognition of U12-dependent introns requires both U11/5' splice-site and U12/branchpoint interactions.

Authors:  M J Frilander; J A Steitz
Journal:  Genes Dev       Date:  1999-04-01       Impact factor: 11.361

2.  The HIV-1 Tat cellular coactivator Tat-SF1 is a general transcription elongation factor.

Authors:  X Y Li; M R Green
Journal:  Genes Dev       Date:  1998-10-01       Impact factor: 11.361

3.  Prp22, a DExH-box RNA helicase, plays two distinct roles in yeast pre-mRNA splicing.

Authors:  B Schwer; C H Gross
Journal:  EMBO J       Date:  1998-04-01       Impact factor: 11.598

Review 4.  Molecular movement inside the translational engine.

Authors:  K S Wilson; H F Noller
Journal:  Cell       Date:  1998-02-06       Impact factor: 41.582

5.  Phosphorylation of spliceosomal protein SAP 155 coupled with splicing catalysis.

Authors:  C Wang; K Chua; W Seghezzi; E Lees; O Gozani; R Reed
Journal:  Genes Dev       Date:  1998-05-15       Impact factor: 11.361

6.  Association of U2 snRNP with the spliceosomal complex E.

Authors:  W Hong; M Bennett; Y Xiao; R Feld Kramer; C Wang; R Reed
Journal:  Nucleic Acids Res       Date:  1997-01-15       Impact factor: 16.971

7.  Partial purification of the yeast U2 snRNP reveals a novel yeast pre-mRNA splicing factor required for pre-spliceosome assembly.

Authors:  F Caspary; A Shevchenko; M Wilm; B Séraphin
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

8.  cDNA cloning of a new member of the FTZ-F1 subfamily from a rainbow trout.

Authors:  M Ito; A Masuda; K Yumoto; A Otomo; Y Takahashi; N Takamatsu; H Kanda; S Yamashita; T Shiba
Journal:  Biochim Biophys Acta       Date:  1998-02-11

9.  Molecular characterization of a novel, widespread nuclear protein that colocalizes with spliceosome components.

Authors:  M S Schmidt-Zachmann; S Knecht; A Krämer
Journal:  Mol Biol Cell       Date:  1998-01       Impact factor: 4.138

10.  CUS2, a yeast homolog of human Tat-SF1, rescues function of misfolded U2 through an unusual RNA recognition motif.

Authors:  D Yan; R Perriman; H Igel; K J Howe; M Neville; M Ares
Journal:  Mol Cell Biol       Date:  1998-09       Impact factor: 4.272

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  35 in total

1.  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

2.  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

3.  The transcription elongation factor CA150 interacts with RNA polymerase II and the pre-mRNA splicing factor SF1.

Authors:  A C Goldstrohm; T R Albrecht; C Suñé; M T Bedford; M A Garcia-Blanco
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

4.  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

5.  Spliceosome assembly pathways for different types of alternative splicing converge during commitment to splice site pairing in the A complex.

Authors:  Matthew V Kotlajich; Tara L Crabb; Klemens J Hertel
Journal:  Mol Cell Biol       Date:  2008-12-08       Impact factor: 4.272

6.  Invariant U2 snRNA nucleotides form a stem loop to recognize the intron early in splicing.

Authors:  Rhonda Perriman; Manuel Ares
Journal:  Mol Cell       Date:  2010-05-14       Impact factor: 17.970

Review 7.  Functional integration of transcriptional and RNA processing machineries.

Authors:  Shatakshi Pandit; Dong Wang; Xiang-Dong Fu
Journal:  Curr Opin Cell Biol       Date:  2008-04-22       Impact factor: 8.382

8.  Characterization of novel SF3b and 17S U2 snRNP proteins, including a human Prp5p homologue and an SF3b DEAD-box protein.

Authors:  Cindy L Will; Henning Urlaub; Tilmann Achsel; Marc Gentzel; Matthias Wilm; Reinhard Lührmann
Journal:  EMBO J       Date:  2002-09-16       Impact factor: 11.598

9.  Rds3p is required for stable U2 snRNP recruitment to the splicing apparatus.

Authors:  Qiang Wang; Brian C Rymond
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

10.  The Isy1p component of the NineTeen complex interacts with the ATPase Prp16p to regulate the fidelity of pre-mRNA splicing.

Authors:  Tommaso Villa; Christine Guthrie
Journal:  Genes Dev       Date:  2005-08-15       Impact factor: 11.361

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