Orb Gene Function in Translational Regulation

描述（由申请人提供）：本提案的主要目标是更好地了解Orb如何自动调节其自身表达，以及它如何控制mRNA编码因子的现场翻译，这些因子对于确定卵母细胞/保育细胞身份和定义卵室和胚胎的极性至关重要。这些问题的部分答案将来自识别和表征对orb自动调节和/或功能重要的其他基因。在形成本申请的基础的实验中，我们使用了两种互补的方法来识别潜在的“辅因子”。在第一个实验中，我们生成了一个敏感的orb突变体背景，可以用来筛选与orb基因“相互作用”的第二个位点突变。第二，我们使用生物化学方法来鉴定体内与Orb相关的蛋白质。我们发现了许多有趣的“候选”基因与这些程序在以前的资助期间。我们还详细描述了其中三个“候选者”，Squid（Sqd），Rasputin（Rin）和dFMR 1。Sqd和Rin作为正调节因子发挥作用，促进Orb表达/活性，而dFMR 1是负调节因子。在即将到来的资助期间，我们建议在我们以前的研究基础上，重点了解这些蛋白质中的每一种如何与其他因素合作来调节Orb的表达/活性。我们的生化实验表明，奥布形成了一系列独特的复合物。由于在这些不同的Orb复合物中发现的许多因子也在我们的遗传筛选中独立鉴定，我们知道Orb相关蛋白可能对Orb功能很重要。我们将集中我们的初步研究与Orb：dFMR 1和（或）Orb：Rin复合物的因素，并将这些因素的特点，使用的方法，在早期的工作中开发的Sqd，Rin和dFMR 1。其他感兴趣的候选人也将使用相同的程序进行研究。为了补充对Orb的分析，我们已经开始分析体细胞Orb样基因orb-2。

DESCRIPTION (provided by applicant): The primary goal of the present proposal is to better understand how Orb auto-regulates its own expression and how it controls the on site translation of mRNAs encoding factors critical for establishing oocyte/nurse cell identity and defining the polarity of the egg chamber and embryo. Part of the answer to these questions will come from identifying and characterizing other genes that are important for orb auto-regulation and/or function. In experiments that form the basis of the present application, we have used two complementary approaches to identify potential "co-factors." In the first we generated a sensitized orb mutant background which could be used to screen for second site mutations that "interact" genetically with orb. In the second, we used a biochemical approach to identify proteins that are associated with Orb in vivo. We uncovered many interesting "candidate" genes with these procedures during the previous grant period. We also characterized three of these "candidates", Squid (Sqd), Rasputin (Rin) and dFMR1 in some detail. Sqd and Rin function as positive regulators, promoting Orb expression/ activity, while dFMR1 is a negative regulator. During the upcoming grant period we propose to build on our previous studies, focusing on understanding how each of these proteins collaborates with other factors to regulate Orb expression/ activity. Our biochemical experiments suggest that Orb forms a series of distinct complexes. Since many of the factors found in these different Orb complexes were also identified independently in our genetic screen, we know that the Orb associated proteins are likely to be important for Orb function. We will focus our initial studies on factors associated with Orb:dFMR1 and(or) Orb:Rin complexes and will characterize these factors using approaches that were developed in earlier work on Sqd, Rin and dFMR1. Other interesting candidates will also be studied using the same procedures. To complement this analysis of Orb, we have begun analyzing the somatic Orb-like gene, orb-2.