Literature DB >> 7753848

General requirement for RNA polymerase II holoenzymes in vivo.

C M Thompson1, R A Young.   

Abstract

Yeast RNA polymerase II holoenzymes have been described that consist of RNA polymerase II, a subset of general transcription factors, and nine SRB regulatory proteins. The feature that distinguishes the RNA polymerase II holoenzymes from other forms of RNA polymerase II in the cell is their tight association with SRB proteins. We investigated the fraction of genes that require SRB proteins in vivo by examining the effect of temperature-sensitive mutations in SRB genes on transcription by RNA polymerase II. Upon transfer to the restrictive temperature, there is a rapid and general shutdown of mRNA synthesis in srb mutant cells. These data, combined with the observation that essentially all of the SRB protein in cells is tightly associated with RNA polymerase II molecules, argue that SRB-containing holoenzymes are the form of RNA polymerase II recruited to most promoters in the cell.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7753848      PMCID: PMC41989          DOI: 10.1073/pnas.92.10.4587

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  38 in total

1.  A mediator required for activation of RNA polymerase II transcription in vitro.

Authors:  P M Flanagan; R J Kelleher; M H Sayre; H Tschochner; R D Kornberg
Journal:  Nature       Date:  1991-04-04       Impact factor: 49.962

2.  Inducing and assaying heat-shock response in Saccharomyces cerevisiae.

Authors:  C M Nicolet; E A Craig
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

3.  A novel transcription factor reveals a functional link between the RNA polymerase II CTD and TFIID.

Authors:  A J Koleske; S Buratowski; M Nonet; R A Young
Journal:  Cell       Date:  1992-05-29       Impact factor: 41.582

4.  Factors involved in specific transcription by mammalian RNA polymerase II. Identification and characterization of factor IIH.

Authors:  O Flores; H Lu; D Reinberg
Journal:  J Biol Chem       Date:  1992-02-05       Impact factor: 5.157

5.  Purification and interaction properties of the human RNA polymerase B(II) general transcription factor BTF2.

Authors:  M Gerard; L Fischer; V Moncollin; J M Chipoulet; P Chambon; J M Egly
Journal:  J Biol Chem       Date:  1991-11-05       Impact factor: 5.157

6.  A general topoisomerase I-dependent transcriptional repression in the stationary phase in yeast.

Authors:  M Choder
Journal:  Genes Dev       Date:  1991-12       Impact factor: 11.361

7.  The TATA-binding protein is required for transcription by all three nuclear RNA polymerases in yeast cells.

Authors:  B P Cormack; K Struhl
Journal:  Cell       Date:  1992-05-15       Impact factor: 41.582

8.  Five intermediate complexes in transcription initiation by RNA polymerase II.

Authors:  S Buratowski; S Hahn; L Guarente; P A Sharp
Journal:  Cell       Date:  1989-02-24       Impact factor: 41.582

9.  A heteromeric transcription factor required for mammalian RNA polymerase II.

Authors:  S Kitajima; Y Tanaka; T Kawaguchi; T Nagaoka; S M Weissman; Y Yasukochi
Journal:  Nucleic Acids Res       Date:  1990-08-25       Impact factor: 16.971

10.  Identification and comparison of stable and unstable mRNAs in Saccharomyces cerevisiae.

Authors:  D Herrick; R Parker; A Jacobson
Journal:  Mol Cell Biol       Date:  1990-05       Impact factor: 4.272

View more
  111 in total

1.  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

2.  Genome-wide association of mediator and RNA polymerase II in wild-type and mediator mutant yeast.

Authors:  Emily Paul; Z Iris Zhu; David Landsman; Randall H Morse
Journal:  Mol Cell Biol       Date:  2014-11-03       Impact factor: 4.272

3.  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

Review 4.  Multi-protein complexes in eukaryotic gene transcription.

Authors:  Ernest Martinez
Journal:  Plant Mol Biol       Date:  2002-12       Impact factor: 4.076

5.  Systematic analysis of essential yeast TAFs in genome-wide transcription and preinitiation complex assembly.

Authors:  Wu-Cheng Shen; Sukesh R Bhaumik; Helen C Causton; Itamar Simon; Xiaochun Zhu; Ezra G Jennings; Tseng-Hsing Wang; Richard A Young; Michael R Green
Journal:  EMBO J       Date:  2003-07-01       Impact factor: 11.598

6.  Targeting of Swi/Snf to the yeast GAL1 UAS G requires the Mediator, TAF IIs, and RNA polymerase II.

Authors:  Karine Lemieux; Luc Gaudreau
Journal:  EMBO J       Date:  2004-09-23       Impact factor: 11.598

7.  In vivo target of a transcriptional activator revealed by fluorescence resonance energy transfer.

Authors:  Sukesh R Bhaumik; Tamal Raha; David P Aiello; Michael R Green
Journal:  Genes Dev       Date:  2004-02-01       Impact factor: 11.361

8.  Distinct role of Mediator tail module in regulation of SAGA-dependent, TATA-containing genes in yeast.

Authors:  Suraiya A Ansari; Mythily Ganapathi; Joris J Benschop; Frank C P Holstege; Joseph T Wade; Randall H Morse
Journal:  EMBO J       Date:  2011-10-04       Impact factor: 11.598

9.  Requirement for a functional interaction between mediator components Med6 and Srb4 in RNA polymerase II transcription.

Authors:  Y C Lee; Y J Kim
Journal:  Mol Cell Biol       Date:  1998-09       Impact factor: 4.272

10.  Activated transcription independent of the RNA polymerase II holoenzyme in budding yeast.

Authors:  J B McNeil; H Agah; D Bentley
Journal:  Genes Dev       Date:  1998-08-15       Impact factor: 11.361

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.