Literature DB >> 9844638

Histone-like TAFs are essential for transcription in vivo.

B Michel1, P Komarnitsky, S Buratowski.   

Abstract

In yeast, the TBP-associated factors (TAFs) Taf17, Taf60, and Taf61(68) resemble histones H3, H4, and H2B, respectively. To analyze their roles in vivo, conditional alleles were isolated by mutagenizing their histone homology domains. Conditional alleles of TAF17 or TAF60 can be specifically suppressed by overexpression of any of the other histone-like TAFs. This and other genetic evidence supports the model of a histone octamer-like structure within TFIID. Shifting strains carrying the conditional TAF alleles to non-permissive conditions results in degradation of TFIID components and the rapid loss of mRNA production. Therefore, in contrast to previous studies in yeast that found only limited roles for TAFs in transcription, we find that the histone-like TAFs are generally required for in vivo transcription.

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Year:  1998        PMID: 9844638     DOI: 10.1016/s1097-2765(00)80164-1

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


  40 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.  Developmental and transcriptional consequences of mutations in Drosophila TAF(II)60.

Authors:  N Aoyagi; D A Wassarman
Journal:  Mol Cell Biol       Date:  2001-10       Impact factor: 4.272

4.  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

5.  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

6.  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

7.  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

8.  TFIIB-facilitated recruitment of preinitiation complexes by a TAF-independent mechanism.

Authors:  Roderick T Hori; Shuping Xu; Xianyuan Hu; Sung Pyo
Journal:  Nucleic Acids Res       Date:  2004-07-22       Impact factor: 16.971

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.  Yeast TFIID serves as a coactivator for Rap1p by direct protein-protein interaction.

Authors:  Krassimira A Garbett; Manish K Tripathi; Belgin Cencki; Justin H Layer; P Anthony Weil
Journal:  Mol Cell Biol       Date:  2006-10-30       Impact factor: 4.272

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