Literature DB >> 14517303

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

Zheng Chen1, James L Manley.   

Abstract

Gene-specific transcriptional activation is a multistep process that requires numerous protein factors and DNA elements, including enhancers and the core promoter. To investigate the roles of core promoter elements in transcriptional activation in vertebrates, we examined expression and factor occupancy on representative promoters in chicken DT40 cells containing a conditional TATA binding protein (TBP)-associated factor 9 allele (TAF9). Characterized core elements, including TATA box-flanking regions and the downstream promoter element, were found to play significant roles in determining promoter strength, response to activators, and factor occupancy and recruitment. The requirement for TAF9 was found to be highly promoter specific, and TAF9 dependence and promoter occupancy were not always correlated. We also describe contrasting examples of factor recruitment and activation mechanisms at different promoters, highlighted by the nearly opposite mechanisms utilized by the simian virus 40 enhancer and p53. With the core promoters analyzed, the former functions by facilitating RNA polymerase II (RNAP II) recruitment to a preassembled TBP/TFIIB-containing scaffold and p53 strongly recruits TBP and TFIIB while RNAP II levels remain modest. Taken together, our results illustrate both the important roles of core promoter elements and the remarkable diversity that characterizes transcriptional activation mechanisms in vertebrates.

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Year:  2003        PMID: 14517303      PMCID: PMC230314          DOI: 10.1128/MCB.23.20.7350-7362.2003

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  74 in total

1.  Core promoter specificities of the Sp1 and VP16 transcriptional activation domains.

Authors:  K H Emami; W W Navarre; S T Smale
Journal:  Mol Cell Biol       Date:  1995-11       Impact factor: 4.272

2.  Cooperation between core promoter elements influences transcriptional activity in vivo.

Authors:  J Colgan; J L Manley
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-14       Impact factor: 11.205

3.  Functional interaction between p53, the TATA-binding protein (TBP), andTBP-associated factors in vivo.

Authors:  G Farmer; J Colgan; Y Nakatani; J L Manley; C Prives
Journal:  Mol Cell Biol       Date:  1996-08       Impact factor: 4.272

4.  The ability to associate with activation domains in vitro is not required for the TATA box-binding protein to support activated transcription in vivo.

Authors:  W P Tansey; W Herr
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-07       Impact factor: 11.205

5.  p53 transcriptional activation mediated by coactivators TAFII40 and TAFII60.

Authors:  C J Thut; J L Chen; R Klemm; R Tjian
Journal:  Science       Date:  1995-01-06       Impact factor: 47.728

6.  Molecular cloning and expression of the 32-kDa subunit of human TFIID reveals interactions with VP16 and TFIIB that mediate transcriptional activation.

Authors:  R D Klemm; J A Goodrich; S Zhou; R Tjian
Journal:  Proc Natl Acad Sci U S A       Date:  1995-06-20       Impact factor: 11.205

7.  Several hydrophobic amino acids in the p53 amino-terminal domain are required for transcriptional activation, binding to mdm-2 and the adenovirus 5 E1B 55-kD protein.

Authors:  J Lin; J Chen; B Elenbaas; A J Levine
Journal:  Genes Dev       Date:  1994-05-15       Impact factor: 11.361

8.  Human TAFII31 protein is a transcriptional coactivator of the p53 protein.

Authors:  H Lu; A J Levine
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-23       Impact factor: 11.205

9.  Mapping Polycomb-repressed domains in the bithorax complex using in vivo formaldehyde cross-linked chromatin.

Authors:  V Orlando; R Paro
Journal:  Cell       Date:  1993-12-17       Impact factor: 41.582

10.  Reversal of in vitro p53 squelching by both TFIIB and TFIID.

Authors:  X Liu; A J Berk
Journal:  Mol Cell Biol       Date:  1995-11       Impact factor: 4.272

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  17 in total

1.  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

2.  The MTE, a new core promoter element for transcription by RNA polymerase II.

Authors:  Chin Yan Lim; Buyung Santoso; Thomas Boulay; Emily Dong; Uwe Ohler; James T Kadonaga
Journal:  Genes Dev       Date:  2004-07-01       Impact factor: 11.361

3.  A core promoter element downstream of the TATA box that is recognized by TFIIB.

Authors:  Wensheng Deng; Stefan G E Roberts
Journal:  Genes Dev       Date:  2005-10-15       Impact factor: 11.361

Review 4.  TFIIB and the regulation of transcription by RNA polymerase II.

Authors:  Wensheng Deng; Stefan G E Roberts
Journal:  Chromosoma       Date:  2007-06-26       Impact factor: 4.316

5.  TFIIB recognition elements control the TFIIA-NC2 axis in transcriptional regulation.

Authors:  Wensheng Deng; Barbora Malecová; Thomas Oelgeschläger; Stefan G E Roberts
Journal:  Mol Cell Biol       Date:  2008-12-29       Impact factor: 4.272

6.  A Filtration-based Method of Preparing High-quality Nuclei from Cross-linked Skeletal Muscle for Chromatin Immunoprecipitation.

Authors:  Kazunari Nohara; Zheng Chen; Seung-Hee Yoo
Journal:  J Vis Exp       Date:  2017-07-06       Impact factor: 1.355

7.  p53 modulates the activity of the GLI1 oncogene through interactions with the shared coactivator TAF9.

Authors:  Joon Won Yoon; Marilyn Lamm; Stephen Iannaccone; Nicole Higashiyama; King Fu Leong; Philip Iannaccone; David Walterhouse
Journal:  DNA Repair (Amst)       Date:  2015-08-01

8.  Variations in intracellular levels of TATA binding protein can affect specific genes by different mechanisms.

Authors:  Stephanie D Bush; Patricia Richard; James L Manley
Journal:  Mol Cell Biol       Date:  2007-10-22       Impact factor: 4.272

9.  Improved Tet-responsive promoters with minimized background expression.

Authors:  Rainer Loew; Niels Heinz; Mathias Hampf; Hermann Bujard; Manfred Gossen
Journal:  BMC Biotechnol       Date:  2010-11-24       Impact factor: 2.563

10.  TIPT2 and geminin interact with basal transcription factors to synergize in transcriptional regulation.

Authors:  Mara E Pitulescu; Martin Teichmann; Lingfei Luo; Michael Kessel
Journal:  BMC Biochem       Date:  2009-06-10       Impact factor: 4.059

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