Glycoregulation of Skp1 in the cytoplasm and nucleus

描述(申请人提供)：进化已经招募了大量的翻译后修饰，以提供对细胞蛋白质机制的时间、空间和功能调节。这个项目专注于一种特定的例子，这种类型似乎是从真核细胞的分泌途径--糖基化--借来的，但实际上可能首先是在细菌细胞的细胞质中进化的。我们认为，复杂的细胞质糖基化在真核生物中发挥着独特的糖调节功能，并且在分泌途径中受到相对于传统蛋白质糖基化的不同控制。最初的分析生物体是社会阿米巴，这里研究的通路的靶标是Skp1，它是E3泛素连接酶SCF类的一个适配器，其靶标经常被磷酸化激活，因此可能需要一种独立的共价调节模式。最值得注意的是，这种修饰包括六个酶促步骤，导致五糖与高度保守的脯氨酸残基相连。这种修饰具有与多肽相媲美的结构丰富性，假设仅针对Skp1并调节其对关键发育转变(高潮)的调节。对Pro-羟基酶表达的遗传操作控制着发育对O2-的需求，这表明该酶在O2-调节中具有正常的作用。最近对Skp1顺序羟脯氨酸依赖的糖基化所需的干扰酶基因的影响的分析为氧依赖的发育的额外水平的分级调控提供了证据，这将在本项目中得到表征。我们最近发现了构建五糖所需的最后一种酶(AgTA)，这使得我们最终能够从遗传和生物化学的角度解决这些想法。首先，我们将在目标1中定义两个1-连接的半乳糖的连接，它们的添加似乎是由AgTA催化的，这将使以后的目标能够化学合成葡聚糖。目的2将研究在添加这两种糖时表现出的AgTA加工性的基础，以及Skp1和AgTA的催化和2-螺旋桨样结构域如何相互调节彼此的活性，假设与质量控制有关。AIM 3将使用糖基化基因的反向遗传和上位性分析来测试分级调控是线性的还是涉及平行的信号通路。此外，将开发新的抗体来监测细胞中Skp1糖基化的进行性变化，这是信号发育的信号。最后，为了确定该修饰途径最重要的功能特征，Aim 4将对人类弓形虫病病原体顶复合体弓形虫Skp1糖调节的进化保守性进行测试。所获得的知识有望产生新的想法，即蛋白质组是如何在选定的原生生物中对外部信号(如O2)和内部信号(如糖代谢物)做出反应的。公共卫生相关性这项研究利用了美国国立卫生研究院的模式生物盘基网原体，这是一种在基因组上与人类寄生虫内阿米巴结盟的社会阿米巴。网柄网柄菌由于其自由生活、无壁生活方式和单倍体基因组，在分子、生化和细胞生物学研究中具有特殊的优势，已被证明是选择各种其他类型原生生物蛋白质糖基化途径的有用模型。一个例子是在这项研究中检查的细胞质糖基化途径。生物信息学和早期生化研究表明，该途径的主要部分存在于植物病原体的大型疫霉群、人类弓形虫感染的病原体和其他原生生物中。由于弓形虫是一种胞内病原体，网柄网柄菌为弓形虫基因的生化和反向遗传分析提供了一个有吸引力的替代宿主，这些基因是该生物体中Skp1修饰途径的候选基因。这将作为未来直接研究弓形虫O2调节途径功能的前奏，弓形虫在人类群体中广泛潜伏传播，如果重新激活，其药物治疗极其有限。

DESCRIPTION (provided by applicant): Evolution has enlisted a large variety of posttranslational modifications to provide temporal, spatial and functional regulation of the protein machinery of the cell. This project focuses on a specific example of a type that has seemingly been borrowed from the secretory pathway of eukaryotic cells, glycosylation, but might actually have first evolved in the cytoplasm of bacterial cells. We propose that complex cytoplasmic glycosylation exerts unique glycoregulatory functions in eukaryotes, and is subject to distinct controls relative to `conventional' protein glycosylation in the secretory pathway. The initial organism of analysis is the social amoeba Dictyostelium, and the target of the pathway studied here is Skp1, an adaptor of the SCF class of E3 ubiquitin ligases whose targets are frequently activated by phosphorylation and for which there may be a need for an independent mode of covalent regulation. Most remarkable is that this modification involves six enzymatic steps resulting in the assembly of a pentasaccharide attached to a highly conserved residue of proline. This modification, with a structural richness rivaling that of a peptide, is hypothesized to target only Skp1 and modulate its regulation of a critical developmental transition (culmination). Genetic manipulation of prolyl hydroxylase expression controls the O2-requirement for development suggesting a normal role for this enzyme in O2-regulation. Recent analysis of the effects of disrupting enzyme genes required for the sequential hydroxyproline-dependent glycosylation of Skp1 gives evidence for additional levels of hierarchical regulation of O2-dependent development, which is to be characterized in this project. Our recent discovery of the last enzyme (AgtA) needed to construct the pentasaccharide has positioned us finally to address these ideas genetically and biochemically. At the outset, we will in aim 1 define the linkages of the two 1-linked galactose sugars whose additions appear to be catalyzed by AgtA, which will enable chemical synthesis of the glycan for the later aims. Aim 2 will examine the basis for apparent AgtA processivity in adding the two sugars, and how Skp1 and the catalytic and 2-propeller-like domains of AgtA mutually regulate each other's activity, hypothesized to be associated with quality control. Aim 3 will employ reverse genetic and epistatic analysis of the glycosylation genes to test whether hierarchical regulation is linear or involves parallel signaling pathways. In addition, new antibodies will be developed to monitor progressive variations in Skp1 glycosylation in the cells which signal development. Finally, to identify the functionally most important features of the modification pathway, aim 4 will carry out tests for the evolutionary conservation of Skp1 glycoregulation in the apicomplexan Toxoplasma gondii, the agent for human toxoplasmosis. The knowledge gained is expected to generate new ideas of how the proteome is regulated in select protists in response to external signals such as O2 and internal signals such as sugar metabolites. PUBLIC HEALTH RELEVANCE The study utilizes the NIH model organism Dictyostelium discoideum, a social amoeba allied genomically with the human parasite Entamoeba. Dictyostelium, which offers special advantages for molecular, biochemical and cell biological studies owing to its free-living, wall-less lifestyle and haploid genome, has proven to be a useful model for select pathways of protein glycosylation of various other types of protists. One example is the cytoplasmic glycosylation pathway examined in this investigation. Bioinformatics and early biochemical studies indicate that the main part of the pathway is present in the large Phytophthora group of plant pathogens, the agent for human toxoplasmosis Toxoplasma gondii, and other protists. Since T. gondii is an intracellular pathogen, Dictyostelium offers an attractive surrogate host for the biochemical and reverse genetic analysis of the Toxoplasma genes that are candidates for the Skp1 modification pathway in this organism. This will serve as a prelude for future direct studies on the function of the pathway for O2-regulation of T. gondii, which is widely disseminated latently in the human population and for which, if it is re-activated, pharmacological therapies are extremely limited.