Literature DB >> 9445475

Transcription factor-specific requirements for coactivators and their acetyltransferase functions.

E Korzus1, J Torchia, D W Rose, L Xu, R Kurokawa, E M McInerney, T M Mullen, C K Glass, M G Rosenfeld.   

Abstract

Different classes of mammalian transcription factors-nuclear receptors, cyclic adenosine 3',5'-monophosphate-regulated enhancer binding protein (CREB), and signal transducer and activator of transcription-1 (STAT-1)-functionally require distinct components of the coactivator complex, including CREB-binding protein (CBP/p300), nuclear receptor coactivators (NCoAs), and p300/CBP-associated factor (p/CAF), based on their platform or assembly properties. Retinoic acid receptor, CREB, and STAT-1 also require different histone acetyltransferase (HAT) activities to activate transcription. Thus, transcription factor-specific differences in configuration and content of the coactivator complex dictate requirements for specific acetyltransferase activities, providing an explanation, at least in part, for the presence of multiple HAT components of the complex.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9445475     DOI: 10.1126/science.279.5351.703

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  172 in total

Review 1.  Regulation of inducible gene expression by the transcription factor NF-kappaB.

Authors:  S Ghosh
Journal:  Immunol Res       Date:  1999       Impact factor: 2.829

2.  Independent repressor domains in ZEB regulate muscle and T-cell differentiation.

Authors:  A A Postigo; D C Dean
Journal:  Mol Cell Biol       Date:  1999-12       Impact factor: 4.272

3.  Targeted histone acetylation and altered nuclease accessibility over short regions of the pea plastocyanin gene.

Authors:  Y L Chua; A P Brown; J C Gray
Journal:  Plant Cell       Date:  2001-03       Impact factor: 11.277

4.  MLL and CREB bind cooperatively to the nuclear coactivator CREB-binding protein.

Authors:  P Ernst; J Wang; M Huang; R H Goodman; S J Korsmeyer
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

5.  Transcriptional activation by NF-kappaB requires multiple coactivators.

Authors:  K A Sheppard; D W Rose; Z K Haque; R Kurokawa; E McInerney; S Westin; D Thanos; M G Rosenfeld; C K Glass; T Collins
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

6.  The p300/CBP acetyltransferases function as transcriptional coactivators of beta-catenin in vertebrates.

Authors:  A Hecht; K Vleminckx; M P Stemmler; F van Roy; R Kemler
Journal:  EMBO J       Date:  2000-04-17       Impact factor: 11.598

7.  Distribution of acetylated histones resulting from Gal4-VP16 recruitment of SAGA and NuA4 complexes.

Authors:  M Vignali; D J Steger; K E Neely; J L Workman
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

8.  p300 requires its histone acetyltransferase activity and SRC-1 interaction domain to facilitate thyroid hormone receptor activation in chromatin.

Authors:  J Li; B W O'Malley; J Wong
Journal:  Mol Cell Biol       Date:  2000-03       Impact factor: 4.272

9.  Factor-specific modulation of CREB-binding protein acetyltransferase activity.

Authors:  V Perissi; J S Dasen; R Kurokawa; Z Wang; E Korzus; D W Rose; C K Glass; M G Rosenfeld
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

10.  The amino-terminal C/H1 domain of CREB binding protein mediates zta transcriptional activation of latent Epstein-Barr virus.

Authors:  D Zerby; C J Chen; E Poon; D Lee; R Shiekhattar; P M Lieberman
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.