Literature DB >> 8774886

Transcription activation in cells lacking TAFIIS.

S S Walker1, J C Reese, L M Apone, M R Green.   

Abstract

The general transcription factor TFIID is composed of the TATA-box-binding protein (TBP) and a set of TBP-associated factors (TAFIIs). In vitro, TAFIIs are required for activated transcription, and have been proposed to be obligatory targets of transcriptional activator proteins (activators)2. The function of TAFIIs has not been investigated systematically in vivo. A Saccharomyces cerevisiae TAFII complex (yTAFII complex) has been identified that shares functional and structural similarities with higher eukaryotic TFIID. In particular, most yTAFIIs are the homologue of a higher eukaryotic TAFII. Here we report that inactivation or depletion of six different yTAFIIs, including the core yTAFII, that contacts TBP, does not compromise transcriptional activation. We conclude that in vivo, activated transcription of many genes can occur in the absence of functional yTAFIIS, and that in these instances another transcription component(s) must be the target of the activator.

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Year:  1996        PMID: 8774886     DOI: 10.1038/383185a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  97 in total

1.  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

2.  Drosophila Mediator complex is broadly utilized by diverse gene-specific transcription factors at different types of core promoters.

Authors:  J M Park; B S Gim; J M Kim; J H Yoon; H S Kim; J G Kang; Y J Kim
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

3.  Requirement for TAF(II)250 acetyltransferase activity in cell cycle progression.

Authors:  E L Dunphy; T Johnson; S S Auerbach; E H Wang
Journal:  Mol Cell Biol       Date:  2000-02       Impact factor: 4.272

4.  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

5.  In vivo requirement of activator-specific binding targets of mediator.

Authors:  J M Park; H S Kim; S J Han; M S Hwang; Y C Lee; Y J Kim
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

6.  The coactivator dTAF(II)110/hTAF(II)135 is sufficient to recruit a polymerase complex and activate basal transcription mediated by CREB.

Authors:  E A Felinski; P G Quinn
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-30       Impact factor: 11.205

7.  The TFIID components human TAF(II)140 and Drosophila BIP2 (TAF(II)155) are novel metazoan homologues of yeast TAF(II)47 containing a histone fold and a PHD finger.

Authors:  Y G Gangloff; J C Pointud; S Thuault; L Carré; C Romier; S Muratoglu; M Brand; L Tora; J L Couderc; I Davidson
Journal:  Mol Cell Biol       Date:  2001-08       Impact factor: 4.272

8.  Association of the Mediator complex with enhancers of active genes.

Authors:  Laurent Kuras; Tilman Borggrefe; Roger D Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-17       Impact factor: 11.205

9.  TFIID and human mediator coactivator complexes assemble cooperatively on promoter DNA.

Authors:  Kristina M Johnson; Jin Wang; Andrea Smallwood; Charina Arayata; Michael Carey
Journal:  Genes Dev       Date:  2002-07-15       Impact factor: 11.361

10.  Activated transcription independent of the RNA polymerase II holoenzyme in budding yeast.

Authors:  J B McNeil; H Agah; D Bentley
Journal:  Genes Dev       Date:  1998-08-15       Impact factor: 11.361

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