Benson M, Pirrotta V
Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030.
EMBO J. 1988 Dec 1;7(12):3907-15. doi: 10.1002/j.1460-2075.1988.tb03277.x.
The Drosophila zeste protein binds in vitro to several sites in the white, Ultrabithorax, decapentaplegic, Antennapedia, and engrailed genes and to at least one site in the zeste gene itself. The distribution of these sites corresponds often with that of regulatory elements in these genes as defined by mutations or, in the case of white, by molecular analysis. A zeste binding site is frequently found in the immediate vicinity of the promoter. zeste binding sites are composed of two or more zeste recognition sequences T/CGAGT/CG. Isolated consensus sequences do not bind or footprint. Cooperative interactions are involved both in binding to a given site and between proteins bound at independent sites. zeste bound to one DNA molecule can in fact bind simultaneously to another DNA molecule. These results suggest a general role for zeste in bringing together distant regulatory elements controlling the activity of a target gene. In this model, transvection effects are a by-product of normal intragenic zeste action.
果蝇zeste蛋白在体外可与白色基因、超双胸基因、五体不全基因、触角足基因和 engrailed基因中的多个位点结合,还可与zeste基因自身的至少一个位点结合。这些位点的分布通常与这些基因中由突变定义的调控元件的分布相对应,对于白色基因而言,则与分子分析所定义的调控元件分布相对应。zeste结合位点常常位于启动子的紧邻区域。zeste结合位点由两个或更多的zeste识别序列T/CGAGT/CG组成。分离的共有序列不具有结合或足迹效应。协同相互作用既参与与给定位点的结合,也参与在独立位点结合的蛋白质之间的相互作用。实际上,与一个DNA分子结合的zeste能够同时与另一个DNA分子结合。这些结果表明zeste在聚集控制靶基因活性的远距离调控元件方面具有普遍作用。在这个模型中,转座效应是正常基因内zeste作用的副产物。