Literature DB >> 9844640

yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex.

K Natarajan1, B M Jackson, E Rhee, A G Hinnebusch.   

Abstract

We obtained a recessive insertion mutation in the gene encoding yeast TBP-associated factor yTAFII61/68 that impairs Gcn4p-independent and Gcn4p-activated HIS3 transcription. This mutation also reduces transcription of seven other class II genes, thus indicating a broad role for this yTAFII in RNA polymerase II transcription. The Gcn4p activation domain interacts with multiple components of the SAGA complex in cell extracts, including the yTAFII proteins associated with SAGA, but not with two yTAFIIs restricted to TFIID. The taf61-1 mutation impairs binding of Gcn4p to SAGA/yTAFII subunits but not to components of holoenzyme mediator. Our results provide strong evidence that recruitment of SAGA, in addition to holoenzyme, is crucial for activation by Gcn4p in vivo and that yTAFII61 plays a key role in this process.

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Year:  1998        PMID: 9844640     DOI: 10.1016/s1097-2765(00)80166-5

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  37 in total

1.  The Spt components of SAGA facilitate TBP binding to a promoter at a post-activator-binding step in vivo.

Authors:  A M Dudley; C Rougeulle; F Winston
Journal:  Genes Dev       Date:  1999-11-15       Impact factor: 11.361

2.  The proteasome regulates the UV-induced activation of the AP-1-like transcription factor Gcn4.

Authors:  M L Stitzel; R Durso; J C Reese
Journal:  Genes Dev       Date:  2001-01-15       Impact factor: 11.361

3.  Histone folds mediate selective heterodimerization of yeast TAF(II)25 with TFIID components yTAF(II)47 and yTAF(II)65 and with SAGA component ySPT7.

Authors:  Y G Gangloff; S L Sanders; C Romier; D Kirschner; P A Weil; L Tora; I Davidson
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

4.  GCN5 dependence of chromatin remodeling and transcriptional activation by the GAL4 and VP16 activation domains in budding yeast.

Authors:  G A Stafford; R H Morse
Journal:  Mol Cell Biol       Date:  2001-07       Impact factor: 4.272

5.  Components of the SAGA histone acetyltransferase complex are required for repressed transcription of ARG1 in rich medium.

Authors:  Andrea R Ricci; Julie Genereaux; Christopher J Brandl
Journal:  Mol Cell Biol       Date:  2002-06       Impact factor: 4.272

6.  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

7.  A mammalian homologue of GCN2 protein kinase important for translational control by phosphorylation of eukaryotic initiation factor-2alpha.

Authors:  R Sood; A C Porter; D A Olsen; D R Cavener; R C Wek
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

8.  The human TFIID components TAF(II)135 and TAF(II)20 and the yeast SAGA components ADA1 and TAF(II)68 heterodimerize to form histone-like pairs.

Authors:  Y G Gangloff; S Werten; C Romier; L Carré; O Poch; D Moras; I Davidson
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

9.  The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation.

Authors:  Malika Saint; Sonal Sawhney; Ishani Sinha; Rana Pratap Singh; Rashmi Dahiya; Anushikha Thakur; Rahul Siddharthan; Krishnamurthy Natarajan
Journal:  Mol Cell Biol       Date:  2014-02-18       Impact factor: 4.272

10.  A triad of subunits from the Gal11/tail domain of Srb mediator is an in vivo target of transcriptional activator Gcn4p.

Authors:  Fan Zhang; Laarni Sumibcay; Alan G Hinnebusch; Mark J Swanson
Journal:  Mol Cell Biol       Date:  2004-08       Impact factor: 4.272

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