Literature DB >> 11940675

Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns.

Doris B Kirschner1, Elmar vom Baur, Christelle Thibault, Steven L Sanders, Yann-Gaël Gangloff, Irwin Davidson, P Anthony Weil, Làszlò Tora.   

Abstract

The RNA polymerase II transcription factor TFIID, composed of the TATA-binding protein (TBP) and TBP-associated factors (TAF(II)s), nucleates preinitiation complex formation at protein-coding gene promoters. SAGA, a second TAF(II)-containing multiprotein complex, is involved in transcription regulation in Saccharomyces cerevisiae. One of the essential protein components common to SAGA and TFIID is yTAF(II)25. We define a minimal evolutionarily conserved 91-amino-acid region of TAF(II)25 containing a histone fold domain that is necessary and sufficient for growth in vivo. Different temperature-sensitive mutations of yTAF(II)25 or chimeras with the human homologue TAF(II)30 arrested cell growth at either the G(1) or G(2)/M cell cycle phase and displayed distinct phenotypic changes and gene expression patterns. Immunoprecipitation studies revealed that TAF(II)25 mutation-dependent gene expression and phenotypic changes correlated at least partially with the integrity of SAGA and TFIID. Genome-wide expression analysis revealed that the five TAF(II)25 temperature-sensitive mutant alleles individually affect the expression of between 18 and 33% of genes, whereas taken together they affect 64% of all class II genes. Thus, different yTAF(II)25 mutations induce distinct phenotypes and affect the regulation of different subsets of genes, demonstrating that no individual TAF(II) mutant allele reflects the full range of its normal functions.

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Year:  2002        PMID: 11940675      PMCID: PMC133751          DOI: 10.1128/MCB.22.9.3178-3193.2002

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  81 in total

1.  TAF25p, a non-histone-like subunit of TFIID and SAGA complexes, is essential for total mRNA gene transcription in vivo.

Authors:  S L Sanders; E R Klebanow; P A Weil
Journal:  J Biol Chem       Date:  1999-07-02       Impact factor: 5.157

Review 2.  Regulation of gene expression by multiple forms of TFIID and other novel TAFII-containing complexes.

Authors:  B Bell; L Tora
Journal:  Exp Cell Res       Date:  1999-01-10       Impact factor: 3.905

3.  The ATM-related cofactor Tra1 is a component of the purified SAGA complex.

Authors:  P A Grant; D Schieltz; M G Pray-Grant; J R Yates; J L Workman
Journal:  Mol Cell       Date:  1998-12       Impact factor: 17.970

4.  Genetic isolation of ADA2: a potential transcriptional adaptor required for function of certain acidic activation domains.

Authors:  S L Berger; B Piña; N Silverman; G A Marcus; J Agapite; J L Regier; S J Triezenberg; L Guarente
Journal:  Cell       Date:  1992-07-24       Impact factor: 41.582

5.  TFIID-specific yeast TAF40 is essential for the majority of RNA polymerase II-mediated transcription in vivo.

Authors:  P B Komarnitsky; B Michel; S Buratowski
Journal:  Genes Dev       Date:  1999-10-01       Impact factor: 11.361

6.  Identification of TATA-binding protein-free TAFII-containing complex subunits suggests a role in nucleosome acetylation and signal transduction.

Authors:  M Brand; K Yamamoto; A Staub; L Tora
Journal:  J Biol Chem       Date:  1999-06-25       Impact factor: 5.157

7.  NuA4, an essential transcription adaptor/histone H4 acetyltransferase complex containing Esa1p and the ATM-related cofactor Tra1p.

Authors:  S Allard; R T Utley; J Savard; A Clarke; P Grant; C J Brandl; L Pillus; J L Workman; J Côté
Journal:  EMBO J       Date:  1999-09-15       Impact factor: 11.598

8.  Mammalian TAF(II)30 is required for cell cycle progression and specific cellular differentiation programmes.

Authors:  D Metzger; E Scheer; A Soldatov; L Tora
Journal:  EMBO J       Date:  1999-09-01       Impact factor: 11.598

9.  Drosophila TAFII40 interacts with both a VP16 activation domain and the basal transcription factor TFIIB.

Authors:  J A Goodrich; T Hoey; C J Thut; A Admon; R Tjian
Journal:  Cell       Date:  1993-11-05       Impact factor: 41.582

10.  Functional analysis of the human estrogen receptor using a phenotypic transactivation assay in yeast.

Authors:  B Pierrat; D M Heery; Y Lemoine; R Losson
Journal:  Gene       Date:  1992-10-01       Impact factor: 3.688

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  18 in total

1.  Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo.

Authors:  Sukesh R Bhaumik; Michael R Green
Journal:  Mol Cell Biol       Date:  2002-11       Impact factor: 4.272

2.  Mapping histone fold TAFs within yeast TFIID.

Authors:  Claire Leurent; Steven Sanders; Christine Ruhlmann; Véronique Mallouh; P Anthony Weil; Doris B Kirschner; Laszlo Tora; Patrick Schultz
Journal:  EMBO J       Date:  2002-07-01       Impact factor: 11.598

3.  Mapping key functional sites within yeast TFIID.

Authors:  Claire Leurent; Steven L Sanders; Màté A Demény; Krassimira A Garbett; Christine Ruhlmann; P Anthony Weil; Làszlò Tora; Patrick Schultz
Journal:  EMBO J       Date:  2004-02-12       Impact factor: 11.598

4.  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

5.  Architecture of the Saccharomyces cerevisiae SAGA transcription coactivator complex.

Authors:  Yan Han; Jie Luo; Jeffrey Ranish; Steven Hahn
Journal:  EMBO J       Date:  2014-09-12       Impact factor: 11.598

6.  Effect of curcumin on aged Drosophila melanogaster: a pathway prediction analysis.

Authors:  Zhi-guo Zhang; Xu-yan Niu; Ai-ping Lu; Gary Guishan Xiao
Journal:  Chin J Integr Med       Date:  2013-10-23       Impact factor: 1.978

7.  Mutations in the histone fold domain of the TAF12 gene show synthetic lethality with the TAF1 gene lacking the TAF N-terminal domain (TAND) by different mechanisms from those in the SPT15 gene encoding the TATA box-binding protein (TBP).

Authors:  Akiko Kobayashi; Tsuyoshi Miyake; Masashi Kawaichi; Tetsuro Kokubo
Journal:  Nucleic Acids Res       Date:  2003-02-15       Impact factor: 16.971

8.  Genome-wide localization analysis of a complete set of Tafs reveals a specific effect of the taf1 mutation on Taf2 occupancy and provides indirect evidence for different TFIID conformations at different promoters.

Authors:  Kazushige Ohtsuki; Koji Kasahara; Katsuhiko Shirahige; Tetsuro Kokubo
Journal:  Nucleic Acids Res       Date:  2009-12-21       Impact factor: 16.971

9.  TAF10 (TAF(II)30) is necessary for TFIID stability and early embryogenesis in mice.

Authors:  William S Mohan; Elisabeth Scheer; Olivia Wendling; Daniel Metzger; Làszlò Tora
Journal:  Mol Cell Biol       Date:  2003-06       Impact factor: 4.272

10.  Quantitative mass spectrometry of TATA binding protein-containing complexes and subunit phosphorylations during the cell cycle.

Authors:  Wwm Pim Pijnappel; Annemieke Kolkman; Marijke Pa Baltissen; Albert Jr Heck; Ht Marc Timmers
Journal:  Proteome Sci       Date:  2009-12-24       Impact factor: 2.480

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