Literature DB >> 7882984

The requirement for the basal transcription factor IIE is determined by the helical stability of promoter DNA.

F C Holstege1, D Tantin, M Carey, P C van der Vliet, H T Timmers.   

Abstract

The role of the basal transcription factor TFIIE was investigated in RNA polymerase II transcription reactions reconstituted with purified proteins. Using negatively supercoiled templates, which circumvent the requirement for TFIIH, we observed that transcription from the adenovirus major-late (ML) core promoter is more dependent on TFIIE than transcription from the adenovirus E4 (E4) or mouse mammary tumor virus (MMTV) promoters. For all three promoters, an increase in the ionic strength of the reaction mixtures led to an increased dependence on TFIIE. Analysis of hybrid ML/MMTV promoters showed that the region encompassing the start site, from -10 to +10, dictates this dependence. Transcription from a relaxed E4 template with a pre-melted -8 to +2 region was completely independent of both TFIIE and TFIIH. We propose that on negatively supercoiled templates TFIIE can facilitate promoter melting.

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Year:  1995        PMID: 7882984      PMCID: PMC398147          DOI: 10.1002/j.1460-2075.1995.tb07059.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  50 in total

1.  Structure of a new nucleic-acid-binding motif in eukaryotic transcriptional elongation factor TFIIS.

Authors:  X Qian; C Jeon; H Yoon; K Agarwal; M A Weiss
Journal:  Nature       Date:  1993-09-16       Impact factor: 49.962

2.  Transcription factors IIE and IIH and ATP hydrolysis direct promoter clearance by RNA polymerase II.

Authors:  J A Goodrich; R Tjian
Journal:  Cell       Date:  1994-04-08       Impact factor: 41.582

Review 3.  Transcriptional activation: a complex puzzle with few easy pieces.

Authors:  R Tjian; T Maniatis
Journal:  Cell       Date:  1994-04-08       Impact factor: 41.582

4.  Factors involved in specific transcription by mammalian RNA polymerase II: purification and characterization of general transcription factor TFIIE.

Authors:  Y Ohkuma; H Sumimoto; M Horikoshi; R G Roeder
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

5.  Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function.

Authors:  L Ma; A Westbroek; A G Jochemsen; G Weeda; A Bosch; D Bootsma; J H Hoeijmakers; A J van der Eb
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

6.  Regulation of TFIIH ATPase and kinase activities by TFIIE during active initiation complex formation.

Authors:  Y Ohkuma; R G Roeder
Journal:  Nature       Date:  1994-03-10       Impact factor: 49.962

7.  Identification of a minimal set of proteins that is sufficient for accurate initiation of transcription by RNA polymerase II.

Authors:  C M Tyree; C P George; L M Lira-DeVito; S L Wampler; M E Dahmus; L Zawel; J T Kadonaga
Journal:  Genes Dev       Date:  1993-07       Impact factor: 11.361

8.  The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor.

Authors:  L Schaeffer; V Moncollin; R Roy; A Staub; M Mezzina; A Sarasin; G Weeda; J H Hoeijmakers; J M Egly
Journal:  EMBO J       Date:  1994-05-15       Impact factor: 11.598

9.  A TATA sequence-dependent transcriptional repressor activity associated with mammalian transcription factor IIA.

Authors:  T Aso; H Serizawa; R C Conaway; J W Conaway
Journal:  EMBO J       Date:  1994-01-15       Impact factor: 11.598

10.  Transcription initiation by RNA polymerase II does not require hydrolysis of the beta-gamma phosphoanhydride bond of ATP.

Authors:  H T Timmers
Journal:  EMBO J       Date:  1994-01-15       Impact factor: 11.598

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  62 in total

Review 1.  DNA wrapping in transcription initiation by RNA polymerase II.

Authors:  B Coulombe
Journal:  Biochem Cell Biol       Date:  1999       Impact factor: 3.626

2.  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

3.  Corepressor required for adenovirus E1B 55,000-molecular-weight protein repression of basal transcription.

Authors:  M E Martin; A J Berk
Journal:  Mol Cell Biol       Date:  1999-05       Impact factor: 4.272

4.  RNA polymerase II holoenzyme modifications accompany transcription reprogramming in herpes simplex virus type 1-infected cells.

Authors:  H L Jenkins; C A Spencer
Journal:  J Virol       Date:  2001-10       Impact factor: 5.103

5.  Analysis of the open region of RNA polymerase II transcription complexes in the early phase of elongation.

Authors:  U Fiedler; H T Timmers
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

6.  RNA polymerase II complexes in the very early phase of transcription are not susceptible to TFIIS-induced exonucleolytic cleavage.

Authors:  Robert Sijbrandi; Ulrike Fiedler; H Th Marc Timmers
Journal:  Nucleic Acids Res       Date:  2002-06-01       Impact factor: 16.971

7.  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

8.  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

9.  Photo-cross-linking of a purified preinitiation complex reveals central roles for the RNA polymerase II mobile clamp and TFIIE in initiation mechanisms.

Authors:  Diane Forget; Marie-France Langelier; Cynthia Thérien; Vincent Trinh; Benoit Coulombe
Journal:  Mol Cell Biol       Date:  2004-02       Impact factor: 4.272

10.  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

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