Literature DB >> 9844637

Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA.

L M Apone1, C A Virbasius, F C Holstege, J Wang, R A Young, M R Green.   

Abstract

The RNA polymerase II general transcription factor TFIID is a multisubunit complex comprising TATA box-binding protein (TBP) and associated factors (TAFIIs). Experiments in yeast have shown that although most TAFIIs are required for viability, many genes are transcribed normally upon inactivation of individual and even multiple yTAFIIs. Here we analyze yTAFII17, recently found to be present in both the SAGA HAT complex as well as TFIID. Functional inactivation of yTAFII17 by temperature-sensitive mutation or depletion results in loss of transcription of many, but not all, genes. The upstream activating sequence (UAS), which contains the activator binding sites, is the region that renders a gene yTAFII17 dependent. In conjunction with previous studies, our results reveal that different TAFIIs have remarkably distinct properties.

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Year:  1998        PMID: 9844637     DOI: 10.1016/s1097-2765(00)80163-x

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


  36 in total

1.  The alpha-helical FXXPhiPhi motif in p53: TAF interaction and discrimination by MDM2.

Authors:  M Uesugi; G L Verdine
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

2.  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

3.  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

4.  Core promoter elements and TAFs contribute to the diversity of transcriptional activation in vertebrates.

Authors:  Zheng Chen; James L Manley
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

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.  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

7.  TFIID and Spt-Ada-Gcn5-acetyltransferase functions probed by genome-wide synthetic genetic array analysis using a Saccharomyces cerevisiae taf9-ts allele.

Authors:  Elena Milgrom; Robert W West; Chen Gao; W-C Winston Shen
Journal:  Genetics       Date:  2005-08-22       Impact factor: 4.562

8.  Domain-wide displacement of histones by activated heat shock factor occurs independently of Swi/Snf and is not correlated with RNA polymerase II density.

Authors:  Jing Zhao; Jorge Herrera-Diaz; David S Gross
Journal:  Mol Cell Biol       Date:  2005-10       Impact factor: 4.272

9.  Displacement of histones at promoters of Saccharomyces cerevisiae heat shock genes is differentially associated with histone H3 acetylation.

Authors:  T Y Erkina; A M Erkine
Journal:  Mol Cell Biol       Date:  2006-10       Impact factor: 4.272

10.  SAGA and Rpd3 chromatin modification complexes dynamically regulate heat shock gene structure and expression.

Authors:  Selena B Kremer; David S Gross
Journal:  J Biol Chem       Date:  2009-09-15       Impact factor: 5.157

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