Dimeric ligands define a role for transcriptional activation domains in reinitiation

被引:232
作者
Ho, SN
Biggar, SR
Spencer, DM
Schreiber, SL
Crabtree, GR
机构
[1] STANFORD UNIV,SCH MED,BECKMAN CTR MOL & GENET MED,HOWARD HUGHES MED INST,DEPT PATHOL,STANFORD,CA 94305
[2] STANFORD UNIV,SCH MED,BECKMAN CTR MOL & GENET MED,HOWARD HUGHES MED INST,DEPT DEV BIOL,STANFORD,CA 94305
[3] HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
关键词
D O I
10.1038/382822a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
EUKARYOTIC transcriptional activators mediate transcriptional induction through stabilization of the preinitiation complex(1-4), probably through direct interactions with basal transcription factors(5-7). In vitro studies on the role of an activator in the maintenance of on-going transcription (reinitiation) hare been contradictory, suggesting that, after formation of a preinitiation complex, an activator may(8) or may not(9) 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.
引用
收藏
页码:822 / 826
页数:5
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