Shykind B M, Kim J, Stewart L, Champoux J J, Sharp P A
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139-4307, USA.
Genes Dev. 1997 Feb 1;11(3):397-407. doi: 10.1101/gad.11.3.397.
The mechanism of coactivation by DNA topoisomerase I (topo I) was examined in a highly defined in vitro transcription system containing Pol II and purified factors. Both stimulation of the basal reaction and coactivation occurred dependent on TAF(II)s. Activation was first observed at the TFIID-TFIIA stage of initiation and maximal activation required the concomitant presence of TFIID, TFIIA, topo I, and activator. Electrophoretic mobility shift assay demonstrated a dramatic enhancement in the formation of the TFIID-TFIIA complex by topo I and activator, dependent on the TAF(II)s. DNase I footprinting confirmed this recruitment. A catalytically inactive topo I, which coactivated transcription, similarly stimulated the rapid formation of the TFIID-TFIIA complex in the presence of activator. A camptothecin-mediated DNA cleavage assay demonstrated the recruitment of topo I to the template by TFIID. Topo I likely functions during activation by enhancing the formation of an active TFIID-TFIIA complex on the promoter.
在一个包含RNA聚合酶II(Pol II)和纯化因子的高度明确的体外转录系统中,研究了DNA拓扑异构酶I(拓扑异构酶I)的共激活机制。基础反应的刺激和共激活都依赖于II型TATA盒结合蛋白(TAF(II)s)而发生。激活首先在起始的TFIID-TFIIA阶段被观察到,最大激活需要TFIID、TFIIA、拓扑异构酶I和激活剂同时存在。电泳迁移率变动分析表明,拓扑异构酶I和激活剂显著增强了TFIID-TFIIA复合物的形成,这依赖于TAF(II)s。DNA酶I足迹法证实了这种募集。一种共激活转录的无催化活性的拓扑异构酶I,在存在激活剂的情况下同样刺激了TFIID-TFIIA复合物的快速形成。喜树碱介导的DNA切割分析表明,TFIID将拓扑异构酶I募集到模板上。拓扑异构酶I可能在激活过程中通过增强启动子上活性TFIID-TFIIA复合物的形成而发挥作用。