Spatial Control of Proteolysis in Dorsoventral Polarity

背腹极性蛋白水解的空间控制

• 批准号: 6868969
• 负责人: ELLEN K LEMOSY
• 金额: $ 24.81万
• 依托单位: AUGUSTA UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-04-01 至 2009-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6868969
• 关键词: Drosophilidae; biological signal transduction; cellular polarity; enzyme activity; enzyme linked immunosorbent assay; fluorescence resonance energy transfer; laboratory rabbit; ligands; mass spectrometry; mucopolysaccharides; oogenesis; protein localization; proteoglycan; proteolysis; toll like receptor; transcription factor; western blottings; zymogens

DESCRIPTION (provided by applicant): The dorsoventral axis of the Drosophila embryo is established by ventral activation of the Toll signaling pathway, resulting in the graded nuclear uptake of the Dorsal transcription factor. Pathway activation relies on a ventral cue synthesized during oogenesis through the action of Pipe, a putative heparan sulfate 2-O- sulfotransferase, on an unknown carbohydrate substrate. In the embryo, the ligand for the receptor Toll is generated by a proteolytic processing reaction involving 4 members of a serine protease cascade, Nude1, Gastrulation Defective (GD), Snake and Easter. Published work has shown that early cascade events occur independently of pipe activity and are not ventrally restricted, while new data shows that activation of the Easter protease requires pipe and is probably ventrally restricted. These observations establish that spatial control occurs within the protease cascade. To investigate the mechanism by which pipe regulates the cascade, three aims are proposed to test the hypothesis that glycosaminoglycans (GAGs) modified by Pipe serve as cofactors promoting the ventral activity of GD and/or Snake. These include: (1) determining where spatial regulation occurs in the protease cascade in vivo, by Western blotting and localization of active proteases; (2) characterizing the functional consequences of GAG interactions with GD and Snake in vitro using purified proteases, and determining whether the specificity of these interactions is consistent with that expected for Pipe-modified GAGs; and (3) identifying GAGs and proteoglycans involved in protease regulation by pipe in vivo, using novel selection strategies to isolate species structurally altered in the absence of pipe. This work is relevant to understanding the regulation of protease cascades, such as those involved in the innate immune response, hemostasis, wound healing, and synaptic plasticity. Additionally, knowledge of how glycosaminoglycan microheterogeneity contributes to patterning is important to understanding the many emerging roles of heparan sulfate proteoglycans in vertebrate and invertebrate development, where, for example, a knock-out of a mouse gene related to pipe results in renal agenesis and skeletal and eye defects.

描述（由申请方提供）：果蝇胚胎的背腹轴是通过腹侧激活Toll信号通路建立的，导致背侧转录因子的分级核摄取。途径激活依赖于卵子发生过程中通过Pipe（一种假定的硫酸乙酰肝素2-O-磺基转移酶）对未知碳水化合物底物的作用合成的腹侧线索。在胚胎中，受体Toll的配体通过涉及丝氨酸蛋白酶级联的4个成员Nude 1、Gastrulation Defective（GD）、Snake和Easter的蛋白水解加工反应产生。已发表的工作表明，早期级联事件发生独立的管道活动，并没有腹侧限制，而新的数据表明，复活节蛋白酶的激活需要管道，可能是腹侧限制。这些观察结果表明，空间控制发生在蛋白酶级联。为了研究管道调节级联的机制，提出了三个目的来检验由管道修饰的糖胺聚糖（GAGs）作为促进GD和/或蛇腹侧活动的辅因子的假设。其中包括：（2）使用纯化的蛋白酶在体外表征GAG与GD和Snake相互作用的功能结果，并确定这些相互作用的特异性是否与Pipe修饰的GAG的预期特异性一致;和（3）使用新的选择策略来分离在没有pipe的情况下结构改变的物种，鉴定体内pipe参与蛋白酶调节的GAG和蛋白聚糖。这项工作与理解蛋白酶级联的调节有关，例如参与先天免疫反应，止血，伤口愈合和突触可塑性的蛋白酶级联。此外，糖胺聚糖微异质性如何有助于图案化的知识对于理解硫酸乙酰肝素蛋白聚糖在脊椎动物和无脊椎动物发育中的许多新兴作用是重要的，例如，敲除与管道相关的小鼠基因导致肾发育不全和骨骼及眼睛缺陷。