Lehmann M, Korge G
Institut für Genetik der Freien Universität Berlin, Germany.
EMBO J. 1996 Sep 16;15(18):4825-34.
Here we describe the identification of four binding sites of secretion enhancer binding protein 2 (SEBP2) in the regulatory region of the Drosophila salivary gland secretion protein gene 4 (Sgs-4) and show that despite these sites' correspondence with previously described Broad-Complex protein binding sites, SEBP2 is a Broad-Complex-independent factor encoded by the region-specific homeotic gene fork head (fkh). Two of the Fork head/SEBP2 binding sites are located within an ecdysone response unit which controls the tissue- and stage-specific responses of Sgs-4 to the steroid hormone 20-hydroxyecdysone. We demonstrate that these binding sites are relevant to the transcriptional activation of Sgs-4 and show that Fork head also binds to the Sgs-4 ecdysone response unit in vivo. Aside from being involved in the control of decisions during embryonic development, fkh thus participates directly in the control of specialized functions of differentiated cells at later stages of development.
在此,我们描述了在果蝇唾液腺分泌蛋白基因4(Sgs-4)调控区域中分泌增强子结合蛋白2(SEBP2)四个结合位点的鉴定,并表明尽管这些位点与先前描述的Broad-Complex蛋白结合位点相对应,但SEBP2是由区域特异性同源异型基因叉头(fkh)编码的不依赖于Broad-Complex的因子。其中两个叉头/SEBP2结合位点位于一个蜕皮激素反应单元内,该单元控制Sgs-4对类固醇激素20-羟基蜕皮激素的组织和阶段特异性反应。我们证明这些结合位点与Sgs-4的转录激活相关,并表明叉头在体内也与Sgs-4蜕皮激素反应单元结合。因此,除了参与胚胎发育过程中的决策控制外,fkh还直接参与发育后期分化细胞特殊功能的控制。