REGULATION OF BETA-CATENIN NUCLEARIZATION

超出所提供的空间。 连环蛋白在特定卵裂球细胞核中的积累是动物发育的关键早期步骤。在所有已研究的后口动物（棘皮动物和脊索动物/脊椎动物）中，_-连环蛋白沿卵裂期胚胎的轴沿着在特定卵裂球的细胞核中积累是胚胎极性的最初指示之一。连环蛋白的这种差异性“核化”对于适当的胚层形成和诱导中心的建立是必不可少的。海胆胚胎是研究β-连环蛋白核化的一个强有力的模型系统。胚胎在外部发育，并且是光学透明的，便于各种光学技术的应用。该系统的独特之处在于可以从早期胚胎中大量分离出特定类型的细胞。大部分的_-连环蛋白途径的分子已被克隆从海胆和大量的分子生物学工具是可用的。基因表达可以通过显性负性构建体的表达和通过显微注射“吗啉代”反义寡核苷酸来操纵。 这项工作将确定早期胚胎中连环蛋白核化的机制。有两个主要目标：1）使用GFP标记的蛋白质和时间推移，3-D共聚焦显微镜，将在体内研究_-连环蛋白降解的关键调节因子的动力学和周转。我们将测量在早期胚胎的特定卵裂球中的_-连环蛋白的半衰期，这将提供关于差异核化的细胞和分子机制的重要信息。通过卵裂球分离实验，我们将测试细胞-细胞相互作用在调节f_-连环蛋白核化中的作用。2)我们将测试沿着胚胎轴的三种主要的GSK 3调节模型。此外，使用显性负性结构和吗啉代，我们将检查GSK 3活性的两个调节因子，disevelled和Akt/PKB的发育ftmction。性能现场=

EXCEED THE SPACE PROVIDED. The accumulation of _-catenin in the nuclei of specific blastomeres is a critical early step in animal development. In all deuterostomes (echinoderms and chordates/vertebrates) that have been studied, accumulation of _-catenin in the nuclei of specific blastomeres along the axis of the cleavage stage embryo is one of the first indications of embryonic polarity. This differential "nuclearization" of _-catenin is essential for proper germ layer formation and the establishment of inductive centers. The sea urchin embryo is a powerful model system for studying _-catenin nuclearization. The embryo develops externally and is optically transparent, facilitating the application of a wide variety of light optical technologies. The system is unique in that specific cell types can be isolated from early embryos in large quantities. Most of the molecules of the _-catenin pathway have been cloned from sea urchin and a large number of molecular biological tools are available. Gene expression can be manipulated by expression of dominant negative constructs and by microinjection of "morpholino" antisense oligonucleotides. The proposed work will identify the mechanisms that underlie _-catenin nuclearization in early embryos. There are two major aims: 1) Using GFP-tagged proteins and time-lapse, 3-D confocal microscopy, the dynamics and turnover of key regulators of _-catenin degradation will be studied in vivo. We will measure the half-life of _-catenin in specific blastomeres of the early embryo, which will provide essential information concerning the cellular and molecular mechanisms of differential nuclearization. Through blastomere isolation experiments, we will test the role of cell-cell interactions in regulating f_-catenin nuclearization. 2) We will test three major models of GSK3 regulation along the embryo axis. In addition, using dominant negative constructs and morpholinos, we will examine the developmental ftmction of two regulators of GSK3 activity, dishevelled and Akt/PKB. PERFORMANCE SITE ========================================Section End===========================================