Rivera-Pomar R, Lu X, Perrimon N, Taubert H, Jäckle H
Abteilung Molekulare Entwicklungsbiologie, Max-Planck-Institut für biophysikalische Chemie, Göttingen, Germany.
Nature. 1995 Jul 20;376(6537):253-6. doi: 10.1038/376253a0.
The process of body prepatterning during Drosophila blastoderm formation relies on the localized activities of zygotic segmentation genes, which are controlled by asymmetrically distributed maternal determinants. The anterior determinant bicoid, a homeodomain transcription factor, forms an anterior-to-posterior concentration gradient. It interacts with the maternal transcription factor hunchback to activate the anterior zygotic patterning genes, including the central gap gene Krüppel (Kr). In contrast, the posterior maternal system does not provide such a decisive transcription factor, but rather prevents the repressor hunchback from acting in the posterior half so that the gap genes giant (gt) and knirps (kni) are activated by an as yet unknown transcription factor. Here we show that caudal, a conserved homeodomain protein that forms a posterior-to-anterior concentration gradient, and the anterior determinant bicoid cooperate to form a partly redundant activator system in the posterior region of the embryo.
果蝇胚盘形成过程中的身体预模式形成过程依赖于合子分割基因的局部活性,这些基因由不对称分布的母体决定因素控制。前部决定因素双胸,一种同源结构域转录因子,形成从前到后的浓度梯度。它与母体转录因子驼背相互作用,以激活前部合子模式形成基因,包括中央间隙基因Krüppel(Kr)。相比之下,后部母体系统并不提供这样一个决定性的转录因子,而是阻止阻遏物驼背在后半部分发挥作用,以便间隙基因巨头(gt)和克尼普斯(kni)由一个尚未知的转录因子激活。在这里,我们表明,尾,一种形成从后到前浓度梯度的保守同源结构域蛋白,与前部决定因素双胸协同作用,在胚胎的后部区域形成一个部分冗余的激活系统。