Literature DB >> 2294406

Polyadenylation-specific complexes undergo a transition early in the polymerization of a poly(A) tail.

V J Bardwell1, M Wickens.   

Abstract

We have analyzed several properties of the complex that forms between RNAs that end at the poly(A) site of simian virus 40 late mRNA and factors present in a HeLa cell nuclear extract. Formation of this polyadenylation-specific complex requires the sequence AAUAAA and a proximal 3' end. We have observed three changes in the polyadenylation complex early in the addition of the poly(A) tail. First, the complex becomes heparin sensitive after the addition of approximately 10 adenosines. Second, a 68-kilodalton protein present in the complex, which can be cross-linked by UV light to the RNA before polyadenylation has begun, no longer can be cross-linked after approximately 10 adenosines have been added. Third, after 30 adenosines have been added, the AAUAAA sequence becomes accessible to a complementary oligonucleotide and RNase H. This accessibility gradually increases with longer poly(A) tail lengths until, with the addition of 60 A's, all substrates are accessible at AAUAAA. Sheets and Wickens (Genes Dev. 3:1401-1412, 1989) have recently demonstrated two phases in the addition of a poly(A) tail: the first requires AAUAAA, whereas the second is independent of AAUAAA but requires a short oligo(A) primer. The data reported here further support a biphasic model for poly(A) addition and may indicate disengagement of specific factors from AAUAAA after the initiation phase.

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Year:  1990        PMID: 2294406      PMCID: PMC360737          DOI: 10.1128/mcb.10.1.295-302.1990

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


  27 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.  Two phases in the addition of a poly(A) tail.

Authors:  M D Sheets; M Wickens
Journal:  Genes Dev       Date:  1989-09       Impact factor: 11.361

Review 3.  Structure and function of bacterial sigma factors.

Authors:  J D Helmann; M J Chamberlin
Journal:  Annu Rev Biochem       Date:  1988       Impact factor: 23.643

4.  Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter.

Authors:  D A Melton; P A Krieg; M R Rebagliati; T Maniatis; K Zinn; M R Green
Journal:  Nucleic Acids Res       Date:  1984-09-25       Impact factor: 16.971

5.  Poly(A) polymerase purified from HeLa cell nuclear extract is required for both cleavage and polyadenylation of pre-mRNA in vitro.

Authors:  G Christofori; W Keller
Journal:  Mol Cell Biol       Date:  1989-01       Impact factor: 4.272

6.  Multiple forms of poly(A) polymerases purified from HeLa cells function in specific mRNA 3'-end formation.

Authors:  L C Ryner; Y Takagaki; J L Manley
Journal:  Mol Cell Biol       Date:  1989-10       Impact factor: 4.272

7.  Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose.

Authors:  H Aviv; P Leder
Journal:  Proc Natl Acad Sci U S A       Date:  1972-06       Impact factor: 11.205

8.  Assembly of a polyadenylation-specific 25S ribonucleoprotein complex in vitro.

Authors:  J E Stefano; D E Adams
Journal:  Mol Cell Biol       Date:  1988-05       Impact factor: 4.272

9.  Multiple factors are required for poly(A) addition to a mRNA 3' end.

Authors:  M A McDevitt; G M Gilmartin; W H Reeves; J R Nevins
Journal:  Genes Dev       Date:  1988-05       Impact factor: 11.361

10.  Two proteins crosslinked to RNA containing the adenovirus L3 poly(A) site require the AAUAAA sequence for binding.

Authors:  C L Moore; J Chen; J Whoriskey
Journal:  EMBO J       Date:  1988-10       Impact factor: 11.598

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  7 in total

1.  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

2.  Ara-ATP impairs 3'-end processing of pre-mRNAs by inhibiting both cleavage and polyadenylation.

Authors:  K Ghoshal; S T Jacob
Journal:  Nucleic Acids Res       Date:  1991-11-11       Impact factor: 16.971

3.  Polyadenylation of mRNA: minimal substrates and a requirement for the 2' hydroxyl of the U in AAUAAA.

Authors:  P L Wigley; M D Sheets; D A Zarkower; M E Whitmer; M Wickens
Journal:  Mol Cell Biol       Date:  1990-04       Impact factor: 4.272

4.  Transcriptional termination in the Balbiani ring 1 gene is closely coupled to 3'-end formation and excision of the 3'-terminal intron.

Authors:  G Baurén; S Belikov; L Wieslander
Journal:  Genes Dev       Date:  1998-09-01       Impact factor: 11.361

5.  The enzyme that adds poly(A) to mRNAs is a classical poly(A) polymerase.

Authors:  V J Bardwell; D Zarkower; M Edmonds; M Wickens
Journal:  Mol Cell Biol       Date:  1990-02       Impact factor: 4.272

6.  Multiple forms of poly(A) polymerases in human cells.

Authors:  A C Thuresson; J Aström; A Aström; K O Grönvik; A Virtanen
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-01       Impact factor: 11.205

7.  Polyadenylation releases mRNA from RNA polymerase II in a process that is licensed by splicing.

Authors:  Frank Rigo; Harold G Martinson
Journal:  RNA       Date:  2009-03-20       Impact factor: 4.942

  7 in total

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