Literature DB >> 1671216

Poly(A) site efficiency reflects the stability of complex formation involving the downstream element.

E A Weiss1, G M Gilmartin, J R Nevins.   

Abstract

A critical step in mRNA biogenesis is the generation of the mRNA 3' end through an endonucleolytic cleavage of the primary transcript followed by the addition of a approximately 200 nucleotide (nt) poly(A) tail. The efficiency of poly(A) site function can vary widely and for those genes with multiple poly(A) sites, the choice can be a regulated event. A functional poly(A) site is characterized by cis-acting RNA sequences including the well-conserved AAUAAA hexamer, located 10-30 nt upstream of the cleavage site, and a highly variable downstream GU- or U-rich element. The gene specific nature of the downstream sequence suggests that it may be a primary determinant of poly(A) site efficiency. Several recent studies have detailed the purification of factors that mediate the cleavage and polyadenylation reaction and that recognize the cis-acting signals. Two of these factors are responsible for the formation of a stable, committed ternary complex with the pre-RNA. In order to define the role of this stable complex in poly(A) site function, we have compared the processing efficiency of several pre-mRNAs with the stability of the complex that forms on these RNAs. We show that ternary complex stability reflects both the in vivo and the in vitro efficiency of the poly(A) site and that the stability of this complex is dependent on the nature of the downstream sequence element. We conclude that the stability of these protein--RNA interactions, dictated by the downstream element, plays a major role in determining the processing efficiency of a particular poly(A) site.

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Year:  1991        PMID: 1671216      PMCID: PMC452632          DOI: 10.1002/j.1460-2075.1991.tb07938.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  27 in total

1.  An ordered pathway of assembly of components required for polyadenylation site recognition and processing.

Authors:  G M Gilmartin; J R Nevins
Journal:  Genes Dev       Date:  1989-12       Impact factor: 11.361

2.  Patterns of polyadenylation site selection in gene constructs containing multiple polyadenylation signals.

Authors:  R M Denome; C N Cole
Journal:  Mol Cell Biol       Date:  1988-11       Impact factor: 4.272

3.  Position-dependent sequence elements downstream of AAUAAA are required for efficient rabbit beta-globin mRNA 3' end formation.

Authors:  A Gil; N J Proudfoot
Journal:  Cell       Date:  1987-05-08       Impact factor: 41.582

4.  Separation and characterization of a poly(A) polymerase and a cleavage/specificity factor required for pre-mRNA polyadenylation.

Authors:  Y Takagaki; L C Ryner; J L Manley
Journal:  Cell       Date:  1988-03-11       Impact factor: 41.582

5.  The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini.

Authors:  J McLauchlan; D Gaffney; J L Whitton; J B Clements
Journal:  Nucleic Acids Res       Date:  1985-02-25       Impact factor: 16.971

6.  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

7.  3' cleavage and polyadenylation of mRNA precursors in vitro requires a poly(A) polymerase, a cleavage factor, and a snRNP.

Authors:  G Christofori; W Keller
Journal:  Cell       Date:  1988-09-09       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.  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.  Sequences capable of restoring poly(A) site function define two distinct downstream elements.

Authors:  M A McDevitt; R P Hart; W W Wong; J R Nevins
Journal:  EMBO J       Date:  1986-11       Impact factor: 11.598

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  63 in total

Review 1.  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

2.  Regulated adenovirus mRNA 3'-end formation in a coupled in vitro transcription-processing system.

Authors:  S I Wilson-Gunn; J E Kilpatrick; M J Imperiale
Journal:  J Virol       Date:  1992-09       Impact factor: 5.103

3.  Two distant upstream regions containing cis-acting signals regulating splicing facilitate 3'-end processing of avian sarcoma virus RNA.

Authors:  J T Miller; C M Stoltzfus
Journal:  J Virol       Date:  1992-07       Impact factor: 5.103

4.  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

5.  Inhibition of HIV-1 replication by eIF3f.

Authors:  Susana T Valente; Greg M Gilmartin; Christina Mott; Brie Falkard; Stephen P Goff
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-23       Impact factor: 11.205

6.  Sequences regulating temporal poly(A) site switching in the adenovirus major late transcription unit.

Authors:  J D DeZazzo; E Falck-Pedersen; M J Imperiale
Journal:  Mol Cell Biol       Date:  1991-12       Impact factor: 4.272

7.  Upstream sequences and cap proximity in the regulation of polyadenylation in ground squirrel hepatitis virus.

Authors:  J Cherrington; R Russnak; D Ganem
Journal:  J Virol       Date:  1992-12       Impact factor: 5.103

8.  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

9.  Sequences homologous to 5' splice sites are required for the inhibitory activity of papillomavirus late 3' untranslated regions.

Authors:  P A Furth; W T Choe; J H Rex; J C Byrne; C C Baker
Journal:  Mol Cell Biol       Date:  1994-08       Impact factor: 4.272

10.  Autoregulation at the level of mRNA 3' end formation of the suppressor of forked gene of Drosophila melanogaster is conserved in Drosophila virilis.

Authors:  A Audibert; M Simonelig
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

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