Collaborative Research: Arabidopsis 2010: Dissecting Cortical Actin Function during Arabidopsis-Pseudomonas Interactions

合作研究：拟南芥 2010：剖析拟南芥-假单胞菌相互作用期间的皮质肌动蛋白功能

• 批准号: 1021463
• 负责人: Jeffrey Chang
• 金额: $ 30.04万
• 依托单位: Oregon State University
• 依托单位国家: 美国
• 项目类别: Continuing Grant
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-15 至 2014-08-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=1021463&HistoricalAwards=false
• 关键词: Collaborative; Research; Arabidopsis; 2010; Dissecting

An exquisite and intricate crosstalk exists between bacterial phytopathogens and the host cells and tissues they invade. New information suggests that a dynamic network of filaments, the cytoskeleton, is essential for both resistance and susceptibility to plant pathogens. However, exactly which molecules from the bacterium stimulate cytoskeletal responses, and which plant proteins are necessary for these responses remains poorly understood. In this project, the investigators will dissect the genetic basis for crosstalk between bacterial effector proteins and the plant host cytoskeleton. Using both molecular genetics tools and advanced imaging technologies, the investigators will test the hypothesis that specific pathogen effector proteins perturb plant actin-binding proteins (ABPs), which in turn leads to alterations in the plant cytoskeleton during defense signaling. A toolbox of actin and actin-binding protein mutants will be developed, and a delivery system for introducing bacterial effectors into host cells will be exploited. Through this work, the PIs aim to identify the function of bacterial effector proteins and 39 plant genes/proteins in order to uncover the signaling network. Lead PI Staiger will coordinate activities between the groups and exploit state-of-the-art imaging modalities to evaluate the defects in actin dynamics in the ABP collection and in response to effector proteins. The Day and Chang laboratories will use genetic approaches to dissect whether crosstalk involves pathogen-associated molecular pattern recognition responses (PTI) or effector-triggered immunity (ETI), or both. These two labs will also use a novel bacterial delivery system to associate changes in actin dynamics to a corresponding bacterial effector protein. The two labs will also prepare constructs for protein-protein interaction assays and subcellular localization. All project data and resources created in this work will be disseminated in a timely fashion at a joint website: http://actinpathogen-network.msu.edu. The broader impact of this work will contribute to a deep understanding of host?pathogen signaling and will enable crop modifications to protect against diseases that devastate agricultural productivity. As a unique outreach component, we will establish a summer workshop to train all project scientists and other interested parties, including local high school students, in advanced methods for imaging cellular dynamics.

细菌植物病原体与它们入侵的宿主细胞和组织之间存在着一种精致而错综复杂的串扰。新的信息表明，一个动态的细丝网络，即细胞骨架，对植物病原体的抗性和敏感性都是必不可少的。然而，细菌中的哪些分子刺激细胞骨架反应，以及哪些植物蛋白是这些反应所必需的，仍然知之甚少。在这个项目中，研究人员将剖析细菌效应蛋白和植物寄主细胞骨架之间串扰的遗传基础。利用分子遗传学工具和先进的成像技术，研究人员将检验特定病原体效应蛋白扰乱植物肌动蛋白结合蛋白(ABPs)的假设，这反过来又会导致植物细胞骨架在防御信号过程中发生变化。将开发肌动蛋白和肌动蛋白结合蛋白突变体的工具箱，并开发将细菌效应物引入宿主细胞的递送系统。通过这项工作，PI旨在鉴定细菌效应蛋白和39个植物基因/蛋白的功能，以揭示信号网络。Lead Pi Staiger将协调小组之间的活动，并利用最先进的成像方法来评估ABP收集中肌动蛋白动力学和对效应器蛋白的反应中的缺陷。戴和张实验室将使用遗传学方法来剖析串扰是否涉及病原体相关的分子模式识别反应(PTI)或效应器触发的免疫(ETI)，或两者兼而有之。这两个实验室还将使用一种新的细菌输送系统，将肌动蛋白动力学的变化与相应的细菌效应蛋白联系起来。这两个实验室还将为蛋白质-蛋白质相互作用分析和亚细胞定位准备结构。在这项工作中创建的所有项目数据和资源将及时在一个联合网站上传播：http://actinpathogen-network.msu.edu.这项工作的更广泛影响将有助于深入了解寄主病原体信号，并将使作物改良能够防止破坏农业生产力的疾病。作为一个独特的推广部分，我们将设立一个暑期研讨会，培训所有项目科学家和其他感兴趣的各方，包括当地的高中生，学习先进的细胞动力学成像方法。