Literature DB >> 1633439

The basic RNA polymerase II transcriptional machinery.

R Weinmann1.   

Abstract

All genes encoding proteins in eukaryotes are transcribed by RNA polymerase II. The first step in analyzing transcriptional regulation requires understanding the general mechanisms of RNA polymerase II-specific gene transcription. The basal promoter, a template containing a TATA box devoid of upstream regulatory sequences, has been used to identify and characterize the factors which, together with RNA polymerase II, govern transcription in mammalian systems: TFIIA, TFIIB, TFIID, TFIIE, TFIIF, TFIIG, TFIIH, and TFIIJ. Interactions between regulatory transcription factors and basal elements of the transcriptional machinery affect the transcriptional rate in a positive or negative fashion. As these multiple proteins are purified, and their coding sequences are isolated, we come closer to reproducing these processes in vitro with pure components, and thus to elucidating the complex interactions among them.

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Year:  1992        PMID: 1633439      PMCID: PMC6057384     

Source DB:  PubMed          Journal:  Gene Expr        ISSN: 1052-2166


  119 in total

1.  Transcriptional repression by YY1, a human GLI-Krüppel-related protein, and relief of repression by adenovirus E1A protein.

Authors:  Y Shi; E Seto; L S Chang; T Shenk
Journal:  Cell       Date:  1991-10-18       Impact factor: 41.582

2.  Binding of general transcription factor TFIIB to an acidic activating region.

Authors:  Y S Lin; I Ha; E Maldonado; D Reinberg; M R Green
Journal:  Nature       Date:  1991-10-10       Impact factor: 49.962

3.  Purification of protein kinases that phosphorylate the repetitive carboxyl-terminal domain of eukaryotic RNA polymerase II.

Authors:  L J Cisek; J L Corden
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

4.  A novel mediator between activator proteins and the RNA polymerase II transcription apparatus.

Authors:  R J Kelleher; P M Flanagan; R D Kornberg
Journal:  Cell       Date:  1990-06-29       Impact factor: 41.582

5.  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

6.  Factors involved in specific transcription by mammalian RNA polymerase II: role of transcription factors IIA, IID, and IIB during formation of a transcription-competent complex.

Authors:  E Maldonado; I Ha; P Cortes; L Weis; D Reinberg
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

7.  Factors involved in specific transcription by mammalian RNA polymerase II. Role of factors IID and MLTF in transcription from the adenovirus major late and IVa2 promoters.

Authors:  J Carcamo; S Lobos; A Merino; L Buckbinder; R Weinmann; V Natarajan; D Reinberg
Journal:  J Biol Chem       Date:  1989-05-05       Impact factor: 5.157

8.  Identification of phosphorylation sites in the repetitive carboxyl-terminal domain of the mouse RNA polymerase II largest subunit.

Authors:  J Zhang; J L Corden
Journal:  J Biol Chem       Date:  1991-02-05       Impact factor: 5.157

9.  A unique structure at the carboxyl terminus of the largest subunit of eukaryotic RNA polymerase II.

Authors:  J L Corden; D L Cadena; J M Ahearn; M E Dahmus
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

10.  RAP30/74: a general initiation factor that binds to RNA polymerase II.

Authors:  Z F Burton; M Killeen; M Sopta; L G Ortolan; J Greenblatt
Journal:  Mol Cell Biol       Date:  1988-04       Impact factor: 4.272

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  10 in total

1.  Isolation and characterization of Aquaporin 1 (AQP1), sodium/potassium-transporting ATPase subunit alpha-1 (Na/K-ATPase α1), Heat Shock Protein 90 (HSP90), Heat Shock Cognate 71 (HSC71), Osmotic Stress Transcription Factor 1 (OSTF1) and Transcription Factor II B (TFIIB) genes from a euryhaline fish, Etroplus suratensis.

Authors:  Wilson Sebastian; Sandhya Sukumaran; P U Zacharia; A Gopalakrishnan
Journal:  Mol Biol Rep       Date:  2018-09-07       Impact factor: 2.316

2.  Unusual charge configurations in transcription factors of the basic RNA polymerase II initiation complex.

Authors:  S Karlin
Journal:  Proc Natl Acad Sci U S A       Date:  1993-06-15       Impact factor: 11.205

3.  The human immunodeficiency virus type 1 long terminal repeat specifies two different transcription complexes, only one of which is regulated by Tat.

Authors:  X Lu; T M Welsh; B M Peterlin
Journal:  J Virol       Date:  1993-04       Impact factor: 5.103

4.  Evidence for a protein domain superfamily shared by the cyclins, TFIIB and RB/p107.

Authors:  T J Gibson; J D Thompson; A Blocker; T Kouzarides
Journal:  Nucleic Acids Res       Date:  1994-03-25       Impact factor: 16.971

5.  C-terminal domain (CTD) of RNA-polymerase II and N-terminal segment of the human TATA binding protein (TBP) can mediate remote and proximal transcriptional activation, respectively.

Authors:  K Seipel; O Georgiev; H P Gerber; W Schaffner
Journal:  Nucleic Acids Res       Date:  1993-12-11       Impact factor: 16.971

Review 6.  Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions.

Authors:  J A Eisen; K S Sweder; P C Hanawalt
Journal:  Nucleic Acids Res       Date:  1995-07-25       Impact factor: 16.971

7.  Identification of a mouse protein whose homolog in Saccharomyces cerevisiae is a component of the CCR4 transcriptional regulatory complex.

Authors:  M P Draper; C Salvadore; C L Denis
Journal:  Mol Cell Biol       Date:  1995-07       Impact factor: 4.272

8.  Modulation of transcriptional activation of the proliferating cell nuclear antigen promoter by the adenovirus E1A 243-residue oncoprotein depends on proximal activators.

Authors:  G F Morris; C Labrie; M B Mathews
Journal:  Mol Cell Biol       Date:  1994-01       Impact factor: 4.272

9.  Sfh1p, a component of a novel chromatin-remodeling complex, is required for cell cycle progression.

Authors:  Y Cao; B R Cairns; R D Kornberg; B C Laurent
Journal:  Mol Cell Biol       Date:  1997-06       Impact factor: 4.272

10.  A C-terminal domain in FosB, absent in FosB/SF and Fra-1, which is able to interact with the TATA binding protein, is required for altered cell growth.

Authors:  R Metz; T Kouzarides; R Bravo
Journal:  EMBO J       Date:  1994-08-15       Impact factor: 11.598

  10 in total

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