Ma X, Yuan D, Diepold K, Scarborough T, Ma J
Division of Developmental Biology, Children's Hospital Research Foundation, Cincinnati, OH 45229-3039, USA.
Development. 1996 Apr;122(4):1195-206. doi: 10.1242/dev.122.4.1195.
The Drosophila morphogenetic protein Bicoid, encoded by the maternal gene bicoid, is required for the development of the anterior structures in the embryo. Bicoid, a transcriptional activator containing a homeodomain, is distributed in an anterior-to-posterior gradient in the embryo. In response to this gradient, the zygotic gene hunchback is expressed uniformly in the anterior half of the embryo in a nearly all-or-none manner. In this report we demonstrate that a recombinant Bicoid protein binds cooperatively to its sites within a hunchback enhancer element. A less than 4-fold increase in Bicoid concentration is sufficient to achieve an unbound/bound transition in DNA binding. Using various biochemical and genetic methods we further demonstrate that Bicoid molecules can interact with each other. Our results are consistent with previous studies performed in the embryo, and they suggest that one mechanism to achieve a sharp on/off switch of gene expression in response to a morphogenetic gradient is cooperative DNA binding facilitated by protein-protein interaction.
由母体基因双胸蛋白(bicoid)编码的果蝇形态发生蛋白双胸蛋白(Bicoid)是胚胎前部结构发育所必需的。双胸蛋白是一种含有同源结构域的转录激活因子,在胚胎中以前后梯度分布。响应于这种梯度,合子基因驼背蛋白(hunchback)在胚胎前半部分以几乎全或无的方式均匀表达。在本报告中,我们证明重组双胸蛋白(Bicoid)与驼背蛋白增强子元件内的位点协同结合。双胸蛋白(Bicoid)浓度增加不到4倍就足以实现DNA结合的未结合/结合转变。使用各种生化和遗传方法,我们进一步证明双胸蛋白(Bicoid)分子可以相互作用。我们的结果与之前在胚胎中进行的研究一致,并且表明响应形态发生梯度实现基因表达的急剧开启/关闭开关的一种机制是由蛋白质-蛋白质相互作用促进的协同DNA结合。