Literature DB >> 7440579

Multiple factors are required for the accurate transcription of purified genes by RNA polymerase III.

J Segall, T Matsui, R G Roeder.   

Abstract

Cell-free extracts (S-100) prepared from cultured mammalian KB cells have previously been shown to direct accurate and selective transcription of class III genes by RNA polymerase III. We have fractionated the KB S-100 and have found that multiple components are essential for the accurate transcription of these genes. After the S-100 has been separated into four different protein fractions by chromatography on phosphocellulose, two fractions are required, in addition to RNA polymerase III, for active and selective transcription of the virus-associated RNAI gene of adenovirus 2 and a tRNA gene; a third fraction is required, along with these components, for the reconstitution of 5 S RNA gene transcription. At least two of these components are distinct from the four factors required for accurate initiation of transcription by RNA polymerase II (Matsui, T., Segall, J., Weil, P. A., and Roeder, R. G. (1980) J. Biol. Chem. 255, 11992-11996).

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Year:  1980        PMID: 7440579

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  151 in total

1.  RNA polymerase III transcription factor IIIB is a target for repression by pocket proteins p107 and p130.

Authors:  J E Sutcliffe; C A Cairns; A McLees; S J Allison; K Tosh; R J White
Journal:  Mol Cell Biol       Date:  1999-06       Impact factor: 4.272

2.  Chromosomal footprinting of transcriptionally active and inactive oocyte-type 5S RNA genes of Xenopus laevis.

Authors:  D R Engelke; J M Gottesfeld
Journal:  Nucleic Acids Res       Date:  1990-10-25       Impact factor: 16.971

3.  The retinoblastoma tumor suppressor protein targets distinct general transcription factors to regulate RNA polymerase III gene expression.

Authors:  H A Hirsch; L Gu; R W Henry
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

4.  Transcription termination by RNA polymerase III: uncoupling of polymerase release from termination signal recognition.

Authors:  F E Campbell; D R Setzer
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

5.  Differential expression of oocyte-type class III genes with fraction TFIIIC from immature or mature oocytes.

Authors:  W F Reynolds; D L Johnson
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

6.  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

7.  A transcriptionally active form of TFIIIC is modified in poliovirus-infected HeLa cells.

Authors:  M E Clark; A Dasgupta
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

8.  Specific transcription of an Acanthamoeba castellanii 5S RNA gene in homologous nuclear extracts.

Authors:  M G Zwick; M A Imboden; M R Paule
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

Review 9.  Contributions of in vitro transcription to the understanding of human RNA polymerase III transcription.

Authors:  Hélène Dumay-Odelot; Stéphanie Durrieu-Gaillard; Leyla El Ayoubi; Camila Parrot; Martin Teichmann
Journal:  Transcription       Date:  2014

10.  Ty3 transposes in mating populations of yeast: a novel transposition assay for Ty3.

Authors:  P T Kinsey; S B Sandmeyer
Journal:  Genetics       Date:  1995-01       Impact factor: 4.562

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