Literature DB >> 10383379

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

S L Sanders1, E R Klebanow, P A Weil.   

Abstract

We demonstrate, utilizing a temperature conditional mutant allele of the gene encoding TAF25p, that this non-histone-like TBP-associated factor, which is shared between the TFIID and SAGA complexes, is required for bulk mRNA gene transcription by RNA polymerase II in vivo. Immunoblotting experiments indicate that at the restrictive temperature, inactivation of TAF25p function results in a reduction of the levels of numerous TFIID and SAGA subunits, indicating its loss of function, like the histone-like TAFs, causes degradation of the constituents of these two multisubunit complexes. These data suggest that TAF25p plays a key structural role in maintaining TFIID and SAGA complex integrity. This is the first demonstration that a non-histone-like TAF is required for continuous, high level RNA polymerase II-mediated mRNA gene transcription in living yeast cells.

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Year:  1999        PMID: 10383379     DOI: 10.1074/jbc.274.27.18847

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  27 in total

1.  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

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.  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

6.  Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells.

Authors:  Lisa S Martel; Helen J Brown; Arnold J Berk
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

7.  TFIIA interacts with TFIID via association with TATA-binding protein and TAF40.

Authors:  S M Kraemer; R T Ranallo; R C Ogg; L A Stargell
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

8.  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

9.  Molecular and genetic characterization of a Taf1p domain essential for yeast TFIID assembly.

Authors:  Madhu V Singh; Christin E Bland; P Anthony Weil
Journal:  Mol Cell Biol       Date:  2004-06       Impact factor: 4.272

10.  Molecular characterization of Saccharomyces cerevisiae TFIID.

Authors:  Steven L Sanders; Krassimira A Garbett; P Anthony Weil
Journal:  Mol Cell Biol       Date:  2002-08       Impact factor: 4.272

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