Schier A F, Gehring W J
Biozentrum der Universität Basel, Switzerland.
Nature. 1992 Apr 30;356(6372):804-7. doi: 10.1038/356804a0.
A major problem in the elucidation of the molecular mechanisms governing development is the distinction between direct and indirect regulatory interactions among developmental control genes. In vivo studies have indicated that the Drosophila segmentation gene fushi tarazu (ftz) directly or indirectly autoregulates its expression. Here we describe a generally applicable experimental approach which establishes a direct in vivo interaction of the homeodomain protein ftz with the ftz cis-autoregulatory control region. In vitro studies have shown that the DNA-binding specificity of the ftz homeodomain can be changed by a single amino-acid substitution in the recognition helix (Gln 50----Lys). Whereas wild-type ftz homeodomain binds preferentially to a CCATTA motif, the mutant homeodomain (ftzQ50K) recognizes a GGATTA motif. We now find that the in vivo activity of an ftz autoregulatory enhancer element is reduced by mutations of putative ftz-binding sites to GGATTA. This down-regulatory effect is specifically suppressed in vivo by the DNA-binding specificity mutant ftzQ50K. These results establish a direct positive autoregulatory feedback mechanism in the regulation of this homeobox gene.
阐明发育调控分子机制的一个主要问题是区分发育控制基因之间直接和间接的调控相互作用。体内研究表明,果蝇体节基因ftz(fushi tarazu)直接或间接自我调节其表达。在此,我们描述了一种普遍适用的实验方法,该方法确定了同源结构域蛋白ftz与ftz顺式自我调节控制区之间的直接体内相互作用。体外研究表明,ftz同源结构域的DNA结合特异性可通过识别螺旋中的单个氨基酸取代(Gln 50→Lys)而改变。野生型ftz同源结构域优先结合CCATTA基序,而突变型同源结构域(ftzQ50K)识别GGATTA基序。我们现在发现,ftz自我调节增强子元件的体内活性因假定的ftz结合位点突变为GGATTA而降低。这种下调效应在体内被DNA结合特异性突变体ftzQ50K特异性抑制。这些结果在该同源框基因的调控中建立了一种直接的正向自我调节反馈机制。