Literature DB >> 2216758

Complex requirements for RNA polymerase III transcription of the Xenopus U6 promoter.

K A Simmen1, I W Mattaj.   

Abstract

The role of various sequences in determining the RNA polymerase III (pol III) specificity of the Xenopus U6 gene promoter has been investigated. A sequence closely resembling an RNA polymerase II (pol II) TATA box, which has previously been implicated in determining the pol III specificity of the U6 promoter, was analyzed in detail. The U6 TATA-like element, in a different promoter context, is shown to be capable of mediating RNA polymerase II transcription both in vitro and in oocyte microinjection experiments. Extensive mutagenesis of the TATA-like element in the context of the pol III and pol II promoters leads to the conclusion that the sequence requirements for function in the two contexts are dissimilar, suggesting that different factors may be involved in mediating pol II and pol III transcription. Further, as implied by the above results, it is shown that the polymerase III specificity of the U6 gene is not solely dependent upon the TATA-like element but rather reflects complex interaction between multiple components of the promoter.

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Year:  1990        PMID: 2216758      PMCID: PMC332296          DOI: 10.1093/nar/18.19.5649

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


  57 in total

1.  E1A-dependent trans-activation of the c-fos promoter requires the TATAA sequence.

Authors:  M C Simon; R J Rooney; T M Fisch; N Heintz; J R Nevins
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

2.  Cloning and structure of a yeast gene encoding a general transcription initiation factor TFIID that binds to the TATA box.

Authors:  M Horikoshi; C K Wang; H Fujii; J A Cromlish; P A Weil; R G Roeder
Journal:  Nature       Date:  1989-09-28       Impact factor: 49.962

3.  Transcription of a human U6 small nuclear RNA gene in vivo withstands deletion of intragenic sequences but not of an upstream TATATA box.

Authors:  G R Kunkel; T Pederson
Journal:  Nucleic Acids Res       Date:  1989-09-25       Impact factor: 16.971

4.  Fine structure genetic analysis of a beta-globin promoter.

Authors:  R M Myers; K Tilly; T Maniatis
Journal:  Science       Date:  1986-05-02       Impact factor: 47.728

5.  The 5S gene internal control region is composed of three distinct sequence elements, organized as two functional domains with variable spacing.

Authors:  T Pieler; J Hamm; R G Roeder
Journal:  Cell       Date:  1987-01-16       Impact factor: 41.582

6.  The SV40 early region TATA box is required for accurate in vitro initiation of transcription.

Authors:  D J Mathis; P Chambon
Journal:  Nature       Date:  1981-03-26       Impact factor: 49.962

7.  Identification of regulatory sequences in the prelude sequences of an H2A histone gene by the study of specific deletion mutants in vivo.

Authors:  R Grosschedl; M L Birnstiel
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

8.  Interaction of a gene-specific transcription factor with the adenovirus major late promoter upstream of the TATA box region.

Authors:  M Sawadogo; R G Roeder
Journal:  Cell       Date:  1985-11       Impact factor: 41.582

9.  A TATA box implicated in E1A transcriptional activation of a simple adenovirus 2 promoter.

Authors:  L Wu; D S Rosser; M C Schmidt; A Berk
Journal:  Nature       Date:  1987 Apr 2-8       Impact factor: 49.962

10.  Drosophila Sgs3 TATA: effects of point mutations on expression in vivo and protein binding in vitro with staged nuclear extracts.

Authors:  A Giangrande; C Mettling; M Martin; C Ruiz; G Richards
Journal:  EMBO J       Date:  1989-11       Impact factor: 11.598

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  7 in total

1.  A role for the TATA-box-binding protein component of the transcription factor IID complex as a general RNA polymerase III transcription factor.

Authors:  R J White; S P Jackson; P W Rigby
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-01       Impact factor: 11.205

2.  The different positioning of the proximal sequence element in the Xenopus RNA polymerase II and III snRNA promoters is a key determinant which confers RNA polymerase III specificity.

Authors:  A Lescure; P Carbon; A Krol
Journal:  Nucleic Acids Res       Date:  1991-02-11       Impact factor: 16.971

3.  Characterization of two developmentally regulated sea urchin U2 small nuclear RNA promoters: a common required TATA sequence and independent proximal and distal elements.

Authors:  B Stefanovic; W F Marzluff
Journal:  Mol Cell Biol       Date:  1992-02       Impact factor: 4.272

4.  Effect of anthracycline antitumor antibiotics (adriamycin and nogalamycin) and cycloheximide on the biosynthesis and processing of major UsnRNAs.

Authors:  R Ray; B K Chakraborty; K Ray; S Mukherji; J R Chowdhury; C K Panda
Journal:  Mol Cell Biochem       Date:  1996-09-06       Impact factor: 3.396

5.  TFIID is required for in vitro transcription of the human U6 gene by RNA polymerase III.

Authors:  K A Simmen; J Bernués; H D Parry; H G Stunnenberg; A Berkenstam; B Cavallini; J M Egly; I W Mattaj
Journal:  EMBO J       Date:  1991-07       Impact factor: 11.598

6.  Transcription of the Xenopus laevis selenocysteine tRNA(Ser)Sec gene: a system that combines an internal B box and upstream elements also found in U6 snRNA genes.

Authors:  P Carbon; A Krol
Journal:  EMBO J       Date:  1991-03       Impact factor: 11.598

7.  Both Arabidopsis TATA binding protein (TBP) isoforms are functionally identical in RNA polymerase II and III transcription in plant cells: evidence for gene-specific changes in DNA binding specificity of TBP.

Authors:  D J Heard; T Kiss; W Filipowicz
Journal:  EMBO J       Date:  1993-09       Impact factor: 11.598

  7 in total

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