Literature DB >> 7518915

Sequence and position requirements for uridylate-rich downstream elements of polyadenylation signals.

Z F Chou1, F Chen, J Wilusz.   

Abstract

We have defined the positional and sequence requirements of U-rich downstream elements using a simian virus 40 late polyadenylation signal containing a substituted downstream region. A UUUUU element will significantly increase the efficiency of 3' end processing when placed between 6 and 25 bases downstream from the cleavage site. Positions in this interval closer than 15 bases from the cleavage site, however, were noticeably less efficient. Placement of the UUUUU element between +20 and +25 caused a partial shift in cleavage site usage to a CA motif at +4. Mutational analysis indicated that the sequence requirements at individual positions of the UUUUU element were somewhat flexible. Changing more than one base of the UUUUU sequence, however, severely diminished the ability of the element to mediate efficient 3' end processing. Finally, although hnRNP C proteins specifically interact with U-rich sequences, this protein--RNA interaction is not required for efficient in vitro polyadenylation.

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Year:  1994        PMID: 7518915      PMCID: PMC308205          DOI: 10.1093/nar/22.13.2525

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  27 in total

Review 1.  The biochemistry of 3'-end cleavage and polyadenylation of messenger RNA precursors.

Authors:  E Wahle; W Keller
Journal:  Annu Rev Biochem       Date:  1992       Impact factor: 23.643

Review 2.  Poly(A) signals.

Authors:  N Proudfoot
Journal:  Cell       Date:  1991-02-22       Impact factor: 41.582

3.  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

4.  An RNA-binding protein specifically interacts with a functionally important domain of the downstream element of the simian virus 40 late polyadenylation signal.

Authors:  Z W Qian; J Wilusz
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

5.  Bipartite structure of the downstream element of the mouse beta globin (major) poly(A) signal.

Authors:  J S Chen; J L Nordstrom
Journal:  Nucleic Acids Res       Date:  1992-05-25       Impact factor: 16.971

6.  Spatial constraints on polyadenylation signal function.

Authors:  C V Heath; R M Denome; C N Cole
Journal:  J Biol Chem       Date:  1990-06-05       Impact factor: 5.157

7.  Sequences upstream of AAUAAA influence poly(A) site selection in a complex transcription unit.

Authors:  J D DeZazzo; M J Imperiale
Journal:  Mol Cell Biol       Date:  1989-11       Impact factor: 4.272

Review 8.  hnRNP proteins and the biogenesis of mRNA.

Authors:  G Dreyfuss; M J Matunis; S Piñol-Roma; C G Burd
Journal:  Annu Rev Biochem       Date:  1993       Impact factor: 23.643

9.  Elements upstream of the AAUAAA within the human immunodeficiency virus polyadenylation signal are required for efficient polyadenylation in vitro.

Authors:  A Valsamakis; N Schek; J C Alwine
Journal:  Mol Cell Biol       Date:  1992-09       Impact factor: 4.272

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

Authors:  E A Weiss; G M Gilmartin; J R Nevins
Journal:  EMBO J       Date:  1991-01       Impact factor: 11.598

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  35 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.  Recruitment of a basal polyadenylation factor by the upstream sequence element of the human lamin B2 polyadenylation signal.

Authors:  S Brackenridge; N J Proudfoot
Journal:  Mol Cell Biol       Date:  2000-04       Impact factor: 4.272

Review 3.  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

4.  Bioinformatic identification of candidate cis-regulatory elements involved in human mRNA polyadenylation.

Authors:  Jun Hu; Carol S Lutz; Jeffrey Wilusz; Bin Tian
Journal:  RNA       Date:  2005-08-30       Impact factor: 4.942

5.  Multiple features contribute to the use of the immunoglobulin M secretion-specific poly(A) signal but are not required for developmental regulation.

Authors:  Martha L Peterson; Gina L Bingham; Clarissa Cowan
Journal:  Mol Cell Biol       Date:  2006-09       Impact factor: 4.272

Review 6.  Protein factors in pre-mRNA 3'-end processing.

Authors:  C R Mandel; Y Bai; L Tong
Journal:  Cell Mol Life Sci       Date:  2008-04       Impact factor: 9.261

7.  The hinge domain of the cleavage stimulation factor protein CstF-64 is essential for CstF-77 interaction, nuclear localization, and polyadenylation.

Authors:  J Andrew Hockert; Hsiang-Jui Yeh; Clinton C MacDonald
Journal:  J Biol Chem       Date:  2009-11-03       Impact factor: 5.157

8.  RNA structure is a critical determinant of poly(A) site recognition by cleavage and polyadenylation specificity factor.

Authors:  B R Graveley; E S Fleming; G M Gilmartin
Journal:  Mol Cell Biol       Date:  1996-09       Impact factor: 4.272

9.  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

10.  Structure of the Rna15 RRM-RNA complex reveals the molecular basis of GU specificity in transcriptional 3'-end processing factors.

Authors:  Christina Pancevac; David C Goldstone; Andres Ramos; Ian A Taylor
Journal:  Nucleic Acids Res       Date:  2010-01-21       Impact factor: 16.971

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