Literature DB >> 1712333

Effect of RNA secondary structure on polyadenylation site selection.

P H Brown1, L S Tiley, B R Cullen.   

Abstract

Functional polyadenylation [poly(A)] sites consist of two sequence elements, the AAUAAA and G/U box signals, that closely flank the site of mRNA 3'-end formation. In agreement with previous results, random sequence insertions between the AAUAAA and G/U box signals were observed to inhibit poly(A) site function. However, sequence insertions of similar size that were predicted to form RNA stem-loop structures were found to have little effect on the efficiency of polyadenylation and instead induced a 3' shift in the site of polyadenylation that was equal to the length of the inserted stem-loop. The in vivo utilization of a poly(A) site bearing an internal RNA stem-loop structure was inhibited by mutations that destabilized the predicted stem but was restored by compensatory mutations. These results strongly support the hypothesis that the appropriate spacing of the AAUAAA and G/U box signals is critical for poly(A) site function. Sequence insertions that are able to form RNA secondary structures that maintain the correct spacing of these two RNA target sequences are well tolerated, whereas sequence insertions that disturb this spacing inhibit poly(A) site recognition. It is proposed that the effect of sequence insertions on poly(A) site function may be sufficiently predictable to allow the development of an assay for in vivo RNA secondary structure that uses poly(A) site selection as a readout.

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Year:  1991        PMID: 1712333     DOI: 10.1101/gad.5.7.1277

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


  23 in total

1.  Recognition efficiency of the hepatitis B virus polyadenylation signals is tissue specific in transgenic mice.

Authors:  S Perfumo; L Amicone; S Colloca; M Giorgio; L Pozzi; M Tripodi
Journal:  J Virol       Date:  1992-11       Impact factor: 5.103

2.  A novel 7-nucleotide motif located in 3' untranslated sequences of the immediate-early gene set mediates platelet-derived growth factor induction of the JE gene.

Authors:  R R Freter; J C Irminger; J A Porter; S D Jones; C D Stiles
Journal:  Mol Cell Biol       Date:  1992-12       Impact factor: 4.272

3.  RNA secondary structure in mutually exclusive splicing.

Authors:  Yun Yang; Leilei Zhan; Wenjing Zhang; Feng Sun; Wenfeng Wang; Nan Tian; Jingpei Bi; Haitao Wang; Dike Shi; Yajian Jiang; Yaozhou Zhang; Yongfeng Jin
Journal:  Nat Struct Mol Biol       Date:  2011-01-09       Impact factor: 15.369

4.  Contributions of the brome mosaic virus RNA-3 3'-nontranslated region to replication and translation.

Authors:  F C Lahser; L E Marsh; T C Hall
Journal:  J Virol       Date:  1993-06       Impact factor: 5.103

5.  Inhibition of polyadenylation by stable RNA secondary structure.

Authors:  B I Klasens; A T Das; B Berkhout
Journal:  Nucleic Acids Res       Date:  1998-04-15       Impact factor: 16.971

Review 6.  Alternative poly(A) site selection in complex transcription units: means to an end?

Authors:  G Edwalds-Gilbert; K L Veraldi; C Milcarek
Journal:  Nucleic Acids Res       Date:  1997-07-01       Impact factor: 16.971

7.  DeepPASTA: deep neural network based polyadenylation site analysis.

Authors:  Ashraful Arefeen; Xinshu Xiao; Tao Jiang
Journal:  Bioinformatics       Date:  2019-11-01       Impact factor: 6.937

8.  Human adenovirus type 5 variants with sequence alterations flanking the E2A gene: effects on E2 expression and DNA replication.

Authors:  C Caravokyri; K N Leppard
Journal:  Virus Genes       Date:  1996       Impact factor: 2.332

9.  Pre-mRNA topology is important for 3'-end formation in Saccharomyces cerevisiae and mammals.

Authors:  G Stumpf; A Goppelt; H Domdey
Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

10.  Polyadenylation site selection cannot occur in vivo after excision of the 3'-terminal intron.

Authors:  X Liu; J E Mertz
Journal:  Nucleic Acids Res       Date:  1993-11-11       Impact factor: 16.971

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