Literature DB >> 9716404

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

J B McNeil1, H Agah, D Bentley.   

Abstract

We investigated whether the multisubunit holoenzyme complex of RNA polymerase II (Pol II) and mediator is universally required for transcription in budding yeast. DeltaCTD Pol II lacking the carboxy-terminal domain of the large subunit cannot assemble with mediator but can still transcribe the CUP1 gene. CUP1 transcripts made by DeltaCTD Pol II initiated correctly and some extended past the normal poly(A) site yielding a novel dicistronic mRNA. Most CUP1 transcripts made by DeltaCTD Pol II were degraded but could be stabilized by deletion of the XRN1 gene. Unlike other genes, transcription of CUP1 and HSP82 also persisted after inactivation of the CTD kinase Kin28 or the mediator subunit Srb4. The upstream-activating sequence (UAS) of the CUP1 promoter was sufficient to drive Cu2+ inducible transcription without Srb4 and heat shock inducible transcription without the CTD. We conclude that the Pol II holoenzyme is not essential for all UAS-dependent activated transcription in yeast.

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Year:  1998        PMID: 9716404      PMCID: PMC317099          DOI: 10.1101/gad.12.16.2510

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  57 in total

1.  RNA polymerase II carboxy-terminal domain contributes to the response to multiple acidic activators in vitro.

Authors:  S M Liao; I C Taylor; R E Kingston; R A Young
Journal:  Genes Dev       Date:  1991-12       Impact factor: 11.361

2.  Eucaryotic RNA polymerase conditional mutant that rapidly ceases mRNA synthesis.

Authors:  M Nonet; C Scafe; J Sexton; R Young
Journal:  Mol Cell Biol       Date:  1987-05       Impact factor: 4.272

3.  Tandemly duplicated upstream control sequences mediate copper-induced transcription of the Saccharomyces cerevisiae copper-metallothionein gene.

Authors:  D J Thiele; D H Hamer
Journal:  Mol Cell Biol       Date:  1986-04       Impact factor: 4.272

4.  RNA polymerase II C-terminal repeat influences response to transcriptional enhancer signals.

Authors:  C Scafe; D Chao; J Lopes; J P Hirsch; S Henry; R A Young
Journal:  Nature       Date:  1990-10-04       Impact factor: 49.962

5.  Nucleosome loss activates CUP1 and HIS3 promoters to fully induced levels in the yeast Saccharomyces cerevisiae.

Authors:  L K Durrin; R K Mann; M Grunstein
Journal:  Mol Cell Biol       Date:  1992-04       Impact factor: 4.272

6.  An RNA polymerase I enhancer in Saccharomyces cerevisiae.

Authors:  E A Elion; J R Warner
Journal:  Mol Cell Biol       Date:  1986-06       Impact factor: 4.272

7.  Transcriptional activation independent of TFIIH kinase and the RNA polymerase II mediator in vivo.

Authors:  D Lee; J T Lis
Journal:  Nature       Date:  1998-05-28       Impact factor: 49.962

8.  Functional redundancy and structural polymorphism in the large subunit of RNA polymerase II.

Authors:  M Nonet; D Sweetser; R A Young
Journal:  Cell       Date:  1987-09-11       Impact factor: 41.582

9.  Role of heat shock transcription factor in yeast metallothionein gene expression.

Authors:  W M Yang; W Gahl; D Hamer
Journal:  Mol Cell Biol       Date:  1991-07       Impact factor: 4.272

10.  A family of low and high copy replicative, integrative and single-stranded S. cerevisiae/E. coli shuttle vectors.

Authors:  N Bonneaud; O Ozier-Kalogeropoulos; G Y Li; M Labouesse; L Minvielle-Sebastia; F Lacroute
Journal:  Yeast       Date:  1991 Aug-Sep       Impact factor: 3.239

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  50 in total

1.  Remodeling of yeast CUP1 chromatin involves activator-dependent repositioning of nucleosomes over the entire gene and flanking sequences.

Authors:  C H Shen; B P Leblanc; J A Alfieri; D J Clark
Journal:  Mol Cell Biol       Date:  2001-01       Impact factor: 4.272

2.  Drosophila Mediator complex is broadly utilized by diverse gene-specific transcription factors at different types of core promoters.

Authors:  J M Park; B S Gim; J M Kim; J H Yoon; H S Kim; J G Kang; Y J Kim
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

3.  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

4.  The CUP1 upstream repeated element renders CUP1 promoter activation insensitive to mutations in the RNA polymerase II transcription complex.

Authors:  Laura Badi; Alcide Barberis
Journal:  Nucleic Acids Res       Date:  2002-03-15       Impact factor: 16.971

5.  T7 RNA polymerase-directed transcripts are processed in yeast and link 3' end formation to mRNA nuclear export.

Authors:  Ken Dower; Michael Rosbash
Journal:  RNA       Date:  2002-05       Impact factor: 4.942

6.  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

7.  Dynamic association of capping enzymes with transcribing RNA polymerase II.

Authors:  S C Schroeder; B Schwer; S Shuman; D Bentley
Journal:  Genes Dev       Date:  2000-10-01       Impact factor: 11.361

Review 8.  Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis.

Authors:  J Zhao; L Hyman; C Moore
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

9.  Cotranscriptional recruitment of the U1 snRNP to intron-containing genes in yeast.

Authors:  Kimberly M Kotovic; Daniel Lockshon; Lamia Boric; Karla M Neugebauer
Journal:  Mol Cell Biol       Date:  2003-08       Impact factor: 4.272

10.  Cdk7 is required for full activation of Drosophila heat shock genes and RNA polymerase II phosphorylation in vivo.

Authors:  Brian E Schwartz; Stephane Larochelle; Beat Suter; John T Lis
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

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