Literature DB >> 2836265

A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II.

S Connelly1, J L Manley.   

Abstract

Polyadenylation of pre-mRNAs requires the conserved hexanucleotide AAUAAA, as well as sequences located downstream from the poly(A) addition site. The role of these sequences in the production of functional mRNAs was studied by analyzing a series of mutants containing deletions or substitutions in the SV40 early region poly(A) site. As expected, both a previously defined GU-rich downstream element and an AAUAAA sequence were required for efficient usage of the wild-type poly(A) addition site. However, when either of these elements was deleted, greatly increased levels of SV40-specific RNA were detected in the nuclei of transfected cells. Evidence is presented that this accumulation of RNA resulted from a failure of transcription termination, leading to multiple rounds of transcription of the circular templates. We conclude that the sequences required for efficient cleavage/polyadenylation of the SV40 early pre-mRNA also constitute an important element of an RNA polymerase II termination signal. A model proposing a mechanism by which the act of pre-mRNA 3' end formation is signaled to the elongating RNA polymerase, resulting in termination, is presented.

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Year:  1988        PMID: 2836265     DOI: 10.1101/gad.2.4.440

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


  157 in total

1.  Transcriptional termination and coupled polyadenylation in vitro.

Authors:  M Yonaha; N J Proudfoot
Journal:  EMBO J       Date:  2000-07-17       Impact factor: 11.598

2.  Mechanism of poly(A) signal transduction to RNA polymerase II in vitro.

Authors:  D P Tran; S J Kim; N J Park; T M Jew; H G Martinson
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

3.  Two distinct forms of the 64,000 Mr protein of the cleavage stimulation factor are expressed in mouse male germ cells.

Authors:  A M Wallace; B Dass; S E Ravnik; V Tonk; N A Jenkins; D J Gilbert; N G Copeland; C C MacDonald
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

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.  Evidence that poly(A) binding protein has an evolutionarily conserved function in facilitating mRNA biogenesis and export.

Authors:  Julia A Chekanova; Dmitry A Belostotsky
Journal:  RNA       Date:  2003-12       Impact factor: 4.942

6.  Independent functions of yeast Pcf11p in pre-mRNA 3' end processing and in transcription termination.

Authors:  Martin Sadowski; Bernhard Dichtl; Wolfgang Hübner; Walter Keller
Journal:  EMBO J       Date:  2003-05-01       Impact factor: 11.598

7.  The primary transcription unit of the human alpha 2 globin gene defined by quantitative RT/PCR.

Authors:  C M Owczarek; P Enriquez-Harris; N J Proudfoot
Journal:  Nucleic Acids Res       Date:  1992-02-25       Impact factor: 16.971

8.  Elongation factor-dependent transcript shortening by template-engaged RNA polymerase II.

Authors:  D Reines
Journal:  J Biol Chem       Date:  1992-02-25       Impact factor: 5.157

9.  Map of cis-acting sequences that determine alternative pre-mRNA processing in the E3 complex transcription unit of adenovirus.

Authors:  H A Brady; A Scaria; W S Wold
Journal:  J Virol       Date:  1992-10       Impact factor: 5.103

10.  Loss of Marek's disease virus tumorigenicity is associated with truncation of RNAs transcribed within BamHI-H.

Authors:  G Bradley; G Lancz; A Tanaka; M Nonoyama
Journal:  J Virol       Date:  1989-10       Impact factor: 5.103

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