Dissecting the role of cellular transport in neurodegeneration using A.nidulans

使用构巢曲霉剖析细胞运输在神经退行性变中的作用

• 批准号: 8522623
• 负责人: Mark Alan McClintock
• 金额: $ 3.39万
• 依托单位: HARVARD MEDICAL SCHOOL
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-03-01 至 2016-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8522623
• 关键词: Actins; Affect; Alzheimer' s Disease; Amyotrophic Lateral Sclerosis; Aspergillus nidulans; Automobile Driving; Axon; Axonal Transport; Behavior; Biological; Biological Models; Biology; Cell Nucleus; Chemicals; Complex; Cytoplasm; Defect; Dendrites; Disease; Dynein ATPase; Etiology; Event; Exhibits; Fibrinogen; Functional disorder; Genetic; Goals; Human; Huntington Disease; Hyphae; Individual; Length; Measurable; Mediating; Methods; Microscope; Microscopy; Microtubules; Modeling; Molds; Mutagenesis; Mutation; Nerve Degeneration; Neurodegenerative Disorders; Neurons; Organelles; Parkinson Disease; Pathogenesis; Pathology; Phenotype; Point Mutation; Process; Production; Proteins; RNA; Reporting; Reproduction spores; Research; Risk Factors; Role; Running; Symptoms; Testing; Toxic effect; Transport Process; Variant; Work; Yeast Model System; Yeasts; base; cell motility; dynactin; genetic manipulation; genome sequencing; insight; mutant; novel; novel strategies; protein TDP-43; protein metabolism; public health relevance; research study; screening; tool

DESCRIPTION (provided by applicant): The long-term research goal of this project is to elucidate common mechanisms by which defects in microtubule-(MT)-based transport promote neurodegenerative disease. Though neurodegenerative diseases are often divergent in symptoms and etiologies, defective long-range transport along MT tracks and the biological dysfunction of the RNA metabolism protein TDP-43 are emerging as common factors associated with a broad range of disorders, including Amyotrophic Lateral Sclerosis (ALS), Alzheimer's disease, and Parkinson's disease. The roles of both TDP-43 and transport defects in driving pathogenesis are poorly understood. The goal of the work proposed here is to investigate the relationship between TDP-43 and long- range transport and determine if they act synergistically to promote disease. Simple and genetically tractable yeast models of TDP-43-based pathology have been valuable, but yeast do not use MTs for long-range cellular transport as humans do and thus are less well suited to dissect is relationship with TDP-43. To understand this relationship, the filamentous fungus A. nidulans will be developed as a model system for studying both TDP- 43-based toxicity and MT-based transport. A. nidulans has genetic tractability comparable to that of yeast, but unlike yeast, uses MTs for long-range transport in cellular regions that closely resemble mammalian neurons. Second, this model will be used to test two alternative hypotheses about the relationship between transport and TDP-43. The first hypothesis is that pathogenic species of TDP-43 broadly impair MT-based transport processes. To test this, MT-based cargos in A. nidulans will be fluorescently-tagged and tracked during TDP- 43 expression in order to detect defects. The second hypothesis is that defects in MT-based transport promote pathogenic features of TDP-43 pathology, such as increased localization to the cytoplasm. This hypothesis will be tested by generating known pathogenic mutations in the MT-based transport machinery and subsequently investigating the biological behavior of TDP-43. Finally, to identify novel factors related to either TDP-43 biology or MT-based transport that contribute to disease, an unbiased and systematic mutagenesis screen will be performed in the A. nidulans pathology model. This work will not only illuminate the causes of TDP-43 based pathology, but also provide a paradigm for elucidating and understanding the pervasive transport defects of neurodegenerative diseases.

描述（由申请人提供）：本项目的长期研究目标是阐明微管（MT）转运缺陷促进神经退行性疾病的常见机制。虽然神经退行性疾病的症状和病因通常是不同的，但沿着沿着MT轨道的有缺陷的长距离运输和RNA代谢蛋白TDP-43的生物功能障碍正在成为与广泛的疾病相关的常见因素，包括肌萎缩性侧索硬化症（ALS）、阿尔茨海默病和帕金森病。TDP-43和转运缺陷在驱动发病机制中的作用知之甚少。本文提出的工作目标是研究TDP-43和长距离运输之间的关系，并确定它们是否协同作用以促进疾病。基于TDP-43的病理学的简单和遗传上易处理的酵母模型是有价值的，但是酵母不像人类那样使用MT进行长距离细胞运输，因此不太适合于剖析与TDP-43的关系。为了理解这种关系，丝状真菌A. nidulans将被开发为用于研究基于TDP- 43的毒性和基于MT的转运的模型系统。A. nidulans具有与酵母相当的遗传易处理性，但与酵母不同的是，它使用MT在非常类似于哺乳动物神经元的细胞区域中进行长距离运输。其次，该模型将被用来测试两个备选假设之间的关系，运输和TDP-43。第一个假设是TDP-43的致病性物种广泛损害基于MT的转运过程。为了验证这一点，在A.在TDP- 43表达过程中，将对构巢蛋白进行荧光标记和跟踪，以检测缺陷。第二个假设是基于MT的转运缺陷促进TDP-43病理学的致病特征，例如增加定位于细胞质。将通过在基于MT的转运机制中产生已知的致病性突变并随后研究TDP-43的生物学行为来检验这一假设。最后，为了鉴定与TDP-43生物学或基于MT的转运相关的导致疾病的新因子，将在A. nidulans病理模型。这项工作不仅将阐明基于TDP-43的病理学的原因，而且还为阐明和理解神经退行性疾病的普遍转运缺陷提供了一个范例。