Literature DB >> 2304466

A multicomponent complex is required for the AAUAAA-dependent cross-linking of a 64-kilodalton protein to polyadenylation substrates.

J Wilusz1, T Shenk, Y Takagaki, J L Manley.   

Abstract

A 64-kilodalton (kDa) polypeptide that is cross-linked by UV light specifically to polyadenylation substrate RNAs containing a functional AAUAAA element has been identified previously. Fractionated HeLa nuclear components that can be combined to regenerate efficient and accurate polyadenylation in vitro have now been screened for the presence of the 64-kDa protein. None of the individual components contained an activity which could generate the 64-kDa species upon UV cross-linking in the presence of substrate RNA. It was necessary to mix two components, cleavage stimulation factor and specificity factor, to reconstitute 64-kDa protein-RNA cross-linking. The addition of cleavage factors to this mixture very efficiently reconstituted the AAUAAA-specific 64-kDa protein-RNA interaction. The 64-kDa protein, therefore, is present in highly purified, reconstituted polyadenylation reactions. However, it is necessary to form a multicomponent complex to efficiently cross-link the protein to a substrate RNA.

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Year:  1990        PMID: 2304466      PMCID: PMC361011          DOI: 10.1128/mcb.10.3.1244-1248.1990

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  41 in total

Review 1.  Transcription termination and 3' processing: the end is in site!

Authors:  M L Birnstiel; M Busslinger; K Strub
Journal:  Cell       Date:  1985-06       Impact factor: 41.582

2.  Accurate and specific polyadenylation of mRNA precursors in a soluble whole-cell lysate.

Authors:  J L Manley
Journal:  Cell       Date:  1983-06       Impact factor: 41.582

3.  The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs.

Authors:  M Fitzgerald; T Shenk
Journal:  Cell       Date:  1981-04       Impact factor: 41.582

4.  3' non-coding region sequences in eukaryotic messenger RNA.

Authors:  N J Proudfoot; G G Brownlee
Journal:  Nature       Date:  1976-09-16       Impact factor: 49.962

5.  Role of the conserved AAUAAA sequence: four AAUAAA point mutants prevent messenger RNA 3' end formation.

Authors:  M Wickens; P Stephenson
Journal:  Science       Date:  1984-11-30       Impact factor: 47.728

6.  Inhibition of RNA cleavage but not polyadenylation by a point mutation in mRNA 3' consensus sequence AAUAAA.

Authors:  C Montell; E F Fisher; M H Caruthers; A J Berk
Journal:  Nature       Date:  1983 Oct 13-19       Impact factor: 49.962

7.  Requirement of a downstream sequence for generation of a poly(A) addition site.

Authors:  M A McDevitt; M J Imperiale; H Ali; J R Nevins
Journal:  Cell       Date:  1984-07       Impact factor: 41.582

8.  Four factors are required for 3'-end cleavage of pre-mRNAs.

Authors:  Y Takagaki; L C Ryner; J L Manley
Journal:  Genes Dev       Date:  1989-11       Impact factor: 11.361

9.  Sequences on the 3' side of hexanucleotide AAUAAA affect efficiency of cleavage at the polyadenylation site.

Authors:  M Sadofsky; J C Alwine
Journal:  Mol Cell Biol       Date:  1984-08       Impact factor: 4.272

10.  Alpha-thalassaemia caused by a polyadenylation signal mutation.

Authors:  D R Higgs; S E Goodbourn; J Lamb; J B Clegg; D J Weatherall; N J Proudfoot
Journal:  Nature       Date:  1983 Nov 24-30       Impact factor: 49.962

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  46 in total

1.  Intercistronic region required for polycistronic pre-mRNA processing in Caenorhabditis elegans.

Authors:  T Huang; S Kuersten; A M Deshpande; J Spieth; M MacMorris; T Blumenthal
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

2.  hnRNP F influences binding of a 64-kilodalton subunit of cleavage stimulation factor to mRNA precursors in mouse B cells.

Authors:  K L Veraldi; G K Arhin; K Martincic; L H Chung-Ganster; J Wilusz; C Milcarek
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

3.  Isolation and characterization of polyadenylation complexes assembled in vitro.

Authors:  K L Veraldi; G Edwalds-Gilbert; C C MacDonald; A M Wallace; C Milcarek
Journal:  RNA       Date:  2000-05       Impact factor: 4.942

Review 4.  Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis.

Authors:  J Zhao; L Hyman; C Moore
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

5.  An uncapped RNA suggests a model for Caenorhabditis elegans polycistronic pre-mRNA processing.

Authors:  Yingmiao Liu; Scott Kuersten; Tao Huang; Alison Larsen; Margaret MacMorris; Thomas Blumenthal
Journal:  RNA       Date:  2003-06       Impact factor: 4.942

6.  Potential role of poly(A) polymerase in the assembly of polyadenylation-specific RNP complexes.

Authors:  M P Terns; S T Jacob
Journal:  Nucleic Acids Res       Date:  1991-01-25       Impact factor: 16.971

7.  The poly A polymerase Star-PAP controls 3'-end cleavage by promoting CPSF interaction and specificity toward the pre-mRNA.

Authors:  Rakesh S Laishram; Richard A Anderson
Journal:  EMBO J       Date:  2010-11-19       Impact factor: 11.598

8.  A uridylate tract mediates efficient heterogeneous nuclear ribonucleoprotein C protein-RNA cross-linking and functionally substitutes for the downstream element of the polyadenylation signal.

Authors:  J Wilusz; T Shenk
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

9.  p54nrb is a component of the snRNP-free U1A (SF-A) complex that promotes pre-mRNA cleavage during polyadenylation.

Authors:  Songchun Liang; Carol S Lutz
Journal:  RNA       Date:  2006-01       Impact factor: 4.942

10.  The upstream sequence element of the C2 complement poly(A) signal activates mRNA 3' end formation by two distinct mechanisms.

Authors:  A Moreira; Y Takagaki; S Brackenridge; M Wollerton; J L Manley; N J Proudfoot
Journal:  Genes Dev       Date:  1998-08-15       Impact factor: 11.361

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