Genetic analysis of FRG1 function in Drosophila

描述(由申请人提供)：面肩肩周肌营养不良症(FSHD)是一种渐进性衰弱综合征，是美国第三大最常见的营养不良类型，但由于我们对其分子基础缺乏了解，定向治疗的发展仍然受阻。使用小鼠模型系统的最新进展表明，FRG1基因的过度表达足以引起一些FSHD症状。因此，降低FRG1的表达和/或功能是治疗干预的一个有前途的途径。几条证据表明，FRG1与RNA剪接机制有关，当过表达时可能会改变正常的剪接，但FRG1的特定生化活性仍不清楚。在这个项目中，我们将利用果蝇黑腹果蝇可用的强大遗传方法来确定FRG1发挥作用的分子途径。利用GAL4-UAS系统，我们将针对FRG1的过度表达而特异性地针对成蝇的间接飞行肌肉。这种肌肉的形态和功能很容易评估，因此它是遗传学研究的理想目标。由于FSHD具有多种肌外效应，我们还将研究FRG1过表达对果蝇复眼的影响，复眼是一种高度有序的组织，经常被用于基因功能分析。利用这些组织中的过度表达表型，我们将进行遗传筛选，以确定能够逆转过度表达FRG1的有害影响的修饰突变。因为这种筛查是以公正的方式进行的，它们提供了确定新的相互作用因素的可能性，否则就不会考虑或调查这些因素。由于之前没有特定的生化活性与FSHD有关，这些因素将为旨在治疗抑制FRG1功能的策略提供新的靶点。在平行研究中，我们将利用已经在果蝇中开发的RNA剪接机制的广泛知识来询问FRG1是否是剪接体的必需组件。使用体外剪接系统，我们将确定剪接和剪接复杂组装的具体步骤和FRG1发挥作用的功能。因此，这些研究将提供果蝇FRG1的第一个遗传和生化分析。通过将果蝇作为FSHD的模型，这项工作将为未来的研究奠定基础，这些研究将详细了解FRG1的正常分子功能及其在肌肉中过度表达的影响。因此，这些研究提供了发现影响肌肉功能和疾病的新的生化途径的可能性。

DESCRIPTION (provided by applicant): Facioscapulohumeral muscular dystrophy (FSHD) is a progressively debilitating syndrome that is the nation's third most common type of dystrophy, yet the development of directed therapies remains hampered by our poor understanding of its molecular basis. Recent progress using a mouse model system suggests that overexpression of the FRG1 gene is sufficient to cause a number of FSHD symptoms. Thus a promising avenue for therapeutic intervention is the reduction of FRG1 expression and/or function. Several lines of evidence suggest that FRG1 associates with the RNA splicing machinery and may alter normal splicing when overexpressed, but the specific biochemical activity of FRG1 remains unknown. In this project we will utilize the powerful genetic approaches available in the fruitfly Drosophila melanogaster to identify molecular pathways through which FRG1 functions. Using the GAL4-UAS system we will target overexpression of FRG1 specifically to the indirect flight muscle of the adult fly. The morphology and function of this muscle are easily assessed and it therefore an ideal target for genetic studies. Because FSHD has a variety of extramuscular effects we will also examine the effects of FRG1 overexpression on the Drosophila compound eye, a highly ordered tissue that is frequently exploited for analysis of gene function. Using overexpression phenotypes in these tissues we will carry out genetic screens to identify modifier mutations that reverse the harmful effects of excess FRG1 expression. Because such screens are carried out in unbiased manner they offer the potential to identify novel interacting factors that would not otherwise have been considered or investigated. As no specific biochemical activity has previously been linked with FSHD, these factors will provide new targets for strategies aimed at therapeutic inhibition of FRG1 function. In parallel studies we will exploit the extensive knowledge of RNA splicing mechanisms already developed in Drosophila to ask whether FRG1 is a required component of the spliceosome. Using an in vitro splicing system we will identify the specific steps in splicing and splicing complex assembly and function where FRG1 acts. These studies will thus provide the first genetic and biochemical analysis of FRG1 in Drosophila. By developing Drosophila as a model for FSHD this work will form a basis for future studies that will elaborate a detailed understanding of both the normal molecular function of FRG1 and the effects of its overexpression in muscle. These studies thus offer the potential to uncover novel biochemical pathways that affect muscle function and disease.