Sauer F, Hansen S K, Tjian R
Science. 1995 Dec 15;270(5243):1783-8. doi: 10.1126/science.270.5243.1783.
Coordinate activation of transcription by multiple enhancer binding factors is essential for the regulation of pattern formation during development of Drosophila melanogaster. Cell-free transcription reactions are described that recapitulate transcriptional synergism directed by the Drosophila developmental regulators Bicoid (BCD) and Hunchback (HB). Within the basal transcription factor complex TFIID, two specific targets, TAFII110 and TAFII60, served as coactivators to mediate transcriptional activation by these two enhancer binding proteins. A quadruple complex containing TATA binding protein (TBP), TAFII250, TAFII110, and TAFII60 mediated transcriptional synergism by BCD and HB, whereas triple TBP-TAFII complexes lacking one or the other target coactivator failed to support synergistic activation. Deoxyribonuclease I footprint protection experiments revealed that an integral step leading to transcriptional synergism involves the recruitment of TBP-TAFII complexes to the promoter by way of multivalent contacts between activators and selected TAFIIs. Thus, the concerted action of multiple regulators with different coactivators helps to establish the pattern and level of segmentation gene transcription during Drosophila development.
多个增强子结合因子对转录的协同激活对于黑腹果蝇发育过程中模式形成的调控至关重要。本文描述了无细胞转录反应,该反应概括了由果蝇发育调节因子双胸蛋白(BCD)和驼背蛋白(HB)指导的转录协同作用。在基础转录因子复合物TFIID中,两个特定靶点TAFII110和TAFII60作为共激活因子,介导这两种增强子结合蛋白的转录激活。一种包含TATA结合蛋白(TBP)、TAFII250、TAFII110和TAFII60的四重复合物介导了BCD和HB的转录协同作用,而缺少其中一个或另一个靶点共激活因子的三重TBP-TAFII复合物则无法支持协同激活。脱氧核糖核酸酶I足迹保护实验表明,导致转录协同作用的一个不可或缺的步骤涉及通过激活因子与选定的TAFII之间的多价接触,将TBP-TAFII复合物募集到启动子上。因此,多个调节因子与不同共激活因子的协同作用有助于在果蝇发育过程中建立分割基因转录的模式和水平。