Ruez C, Payre F, Vincent A
Centre de Biologie du Développement, UMR 5547 CNRS/UPS, Bat 4R3, 118 route de Narbonne, 31062, Toulouse cedex 4, France.
Mech Dev. 1998 Nov;78(1-2):125-34. doi: 10.1016/s0925-4773(98)00159-2.
Concentration of maternal BICOID (BCD) establishes the anterior pattern in the Drosophila embryo. Successive deletions in the bcd promoter allowed us to localize an enhancer sequence in the 5'-UTR and a down-regulating element downstream of the ATG initiator codon, and identify a 49 bp region sufficient to drive transcription of a reporter gene specifically in nurse cells. This fragment contains two binding sites for the Serendipity (Sry) d zinc finger activator, that mediate its cooperative binding. Both sites (sdbs) are essential for bcd expression. Further analysis showed that the bcd promoter configuration is decisive for Sry d activating function. Replacement of sdbs by binding sites for Sry b, the Sry d paralog, restores bcd transcription in sry d mutant ovaries, demonstrating that the functional divergence between these two proteins during evolution was mainly driven by changes in their DNA-specific recognition properties, resulting in the control of separate developmental pathways.
母体双尾(BCD)的浓度在果蝇胚胎中建立了前部模式。bcd启动子的连续缺失使我们能够在5'-UTR中定位一个增强子序列以及ATG起始密码子下游的一个下调元件,并鉴定出一个49bp的区域,该区域足以驱动报告基因在滋养细胞中特异性转录。该片段包含两个用于偶然(Sry)d锌指激活剂的结合位点,介导其协同结合。这两个位点(sdbs)对于bcd表达至关重要。进一步的分析表明,bcd启动子构型对于Sry d激活功能具有决定性作用。用Sry b(Sry d的旁系同源物)的结合位点取代sdbs可恢复sry d突变卵巢中的bcd转录,表明这两种蛋白质在进化过程中的功能差异主要是由它们的DNA特异性识别特性的变化驱动的,从而导致对不同发育途径的控制。