Literature DB >> 8752278

Dimeric ligands define a role for transcriptional activation domains in reinitiation.

S N Ho1, S R Biggar, D M Spencer, S L Schreiber, G R Crabtree.   

Abstract

Eukaryotic transcriptional activators mediate transcriptional induction through stabilization of the preinitiation complex, probably through direct interactions with basal transcription factors. In vitro studies on the role of an activator in the maintenance of on-going transcription (reinitiation) have been contradictory, suggesting that, after formation of a preinitiation complex, an activator may or may not be necessary for transcription to be maintained. We have developed a means of regulating transcription in living cells through the use of both homodimeric and heterodimerizing synthetic ligands that allow the ligand-dependent association and disassociation of a transcriptional activation domain with a promoter. Here we report that maintaining the transcription of endogenous genes in vivo, in both yeast and human cells, requires the continuous presence of the activation domain. The use of synthetic ligands as a transcriptional on-off switch represents a powerful means of controlling the transcription in vitro and in vivo for both experimental and therapeutic purposes.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8752278     DOI: 10.1038/382822a0

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


  67 in total

1.  A ligand-reversible dimerization system for controlling protein-protein interactions.

Authors:  C T Rollins; V M Rivera; D N Woolfson; T Keenan; M Hatada; S E Adams; L J Andrade; D Yaeger; M R van Schravendijk; D A Holt; M Gilman; T Clackson
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

2.  Protein-protein interactions monitored in mammalian cells via complementation of beta -lactamase enzyme fragments.

Authors:  Tom Wehrman; Benjamin Kleaveland; Jeng-Horng Her; Robert F Balint; Helen M Blau
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-19       Impact factor: 11.205

3.  The nucleosome remodeling complex, Snf/Swi, is required for the maintenance of transcription in vivo and is partially redundant with the histone acetyltransferase, Gcn5.

Authors:  P Sudarsanam; Y Cao; L Wu; B C Laurent; F Winston
Journal:  EMBO J       Date:  1999-06-01       Impact factor: 11.598

4.  Inducible gene expression and protein translocation using nontoxic ligands identified by a mammalian three-hybrid screen.

Authors:  S D Liberles; S T Diver; D J Austin; S L Schreiber
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-22       Impact factor: 11.205

5.  The Cyc8-Tup1 complex inhibits transcription primarily by masking the activation domain of the recruiting protein.

Authors:  Koon Ho Wong; Kevin Struhl
Journal:  Genes Dev       Date:  2011-12-01       Impact factor: 11.361

6.  An adaptable luminescence resonance energy transfer assay for measuring and screening protein-protein interactions and their inhibition.

Authors:  Engin Yapici; D Rajasekhar Reddy; Lawrence W Miller
Journal:  Chembiochem       Date:  2012-01-23       Impact factor: 3.164

7.  Small molecule control of pre-mRNA splicing.

Authors:  Brenton R Graveley
Journal:  RNA       Date:  2005-01-20       Impact factor: 4.942

8.  Self-organization vs Watchmaker: stochastic gene expression and cell differentiation.

Authors:  Alexei Kurakin
Journal:  Dev Genes Evol       Date:  2004-11-30       Impact factor: 0.900

9.  Exploiting protein destruction for constructive use.

Authors:  Kryn Stankunas; Gerald R Crabtree
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-02       Impact factor: 11.205

10.  A FRET-facilitated photoswitching using an orange fluorescent protein with the fast photoconversion kinetics.

Authors:  Oksana M Subach; David Entenberg; John S Condeelis; Vladislav V Verkhusha
Journal:  J Am Chem Soc       Date:  2012-08-27       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.