Literature DB >> 8490964

DNA topology and a minimal set of basal factors for transcription by RNA polymerase II.

J D Parvin1, P A Sharp.   

Abstract

Immunoglobulin heavy chain (IgH) gene transcription in vitro can be reconstituted with a minimal reaction containing only TATA-binding protein (TBP), TFIIB, and RNA polymerase II (pol II) when the template is negatively supercoiled. Transcription from linear DNA templates containing either the IgH or the adenovirus major late promoters (MLPs) requires in addition TFIIF, TFIIE, TFIIH, and a fraction containing TFIIA and TFIIJ. Promoters vary in their activities in the minimal reaction. Initiation at the adenovirus MLP site was not observed in this reaction, even with templates containing negative superhelical density. When only TBP, TFIIB, and pol II were present in the reaction, the more negatively supercoiled the IgH template DNA was, the more active the transcription. It is suggested that the free energy of supercoiling promotes the formation of an open complex for initiation of transcription by the minimal set of transcription factors.

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Year:  1993        PMID: 8490964     DOI: 10.1016/0092-8674(93)90140-l

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  144 in total

1.  The general transcription factors IIA, IIB, IIF, and IIE are required for RNA polymerase II transcription from the human U1 small nuclear RNA promoter.

Authors:  T C Kuhlman; H Cho; D Reinberg; N Hernandez
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

2.  Marking the start site of RNA polymerase III transcription: the role of constraint, compaction and continuity of the transcribed DNA strand.

Authors:  Anne Grove; Morgan S Adessa; E Peter Geiduschek; George A Kassavetis
Journal:  EMBO J       Date:  2002-02-15       Impact factor: 11.598

3.  Promoter opening by sigma(54) and sigma(70) RNA polymerases: sigma factor-directed alterations in the mechanism and tightness of control.

Authors:  Y Guo; C M Lew; J D Gralla
Journal:  Genes Dev       Date:  2000-09-01       Impact factor: 11.361

4.  An initiation element in the yeast CUP1 promoter is recognized by RNA polymerase II in the absence of TATA box-binding protein if the DNA is negatively supercoiled.

Authors:  B P Leblanc; C J Benham; D J Clark
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-26       Impact factor: 11.205

5.  Molecular mechanism of recruitment of TFIIF- associating RNA polymerase C-terminal domain phosphatase (FCP1) by transcription factor IIF.

Authors:  Katsuhiko Kamada; Robert G Roeder; Stephen K Burley
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-18       Impact factor: 11.205

6.  Genetic analysis of the large subunit of yeast transcription factor IIE reveals two regions with distinct functions.

Authors:  N H Kuldell; S Buratowski
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

7.  Mechanism of promoter melting by the xeroderma pigmentosum complementation group B helicase of transcription factor IIH revealed by protein-DNA photo-cross-linking.

Authors:  M Douziech; F Coin; J M Chipoulet; Y Arai; Y Ohkuma; J M Egly; B Coulombe
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

8.  Inactivated RNA polymerase II open complexes can be reactivated with TFIIE.

Authors:  Pavel Čabart; Donal S Luse
Journal:  J Biol Chem       Date:  2011-11-27       Impact factor: 5.157

9.  Revealing the functions of TFIIB.

Authors:  Robert O J Weinzierl; Simone C Wiesler
Journal:  Transcription       Date:  2011-11-01

10.  Mechanism of start site selection by RNA polymerase II: interplay between TFIIB and Ssl2/XPB helicase subunit of TFIIH.

Authors:  Shivani Goel; Shankarling Krishnamurthy; Michael Hampsey
Journal:  J Biol Chem       Date:  2011-11-11       Impact factor: 5.157

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