Post-Embryonic Development of the Drosophila Brain

果蝇大脑的胚胎后发育

• 批准号: 7017052
• 负责人: TZUMIN LEE
• 金额: $ 36.58万
• 依托单位: UNIV OF MASSACHUSETTS MED SCH WORCESTER
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-08-01 至 2010-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7017052
• 关键词: Drosophilidae; animal genetic material tag; axon; brain; cell cell interaction; cell population study; dendrites; developmental genetics; developmental neurobiology; gene expression; gene mutation; genetic mapping; glia; histogenesis; metamorphosis; molecular cloning; mutant; nerve /myelin protein; neurogenesis; neurogenetics; neuronal guidance; protein isoforms; protein localization; technology /technique development; transfection

DESCRIPTION (provided by applicant): Brain development involves orderly generation of distinct types of neurons, establishment of stereotyped neuronal connections, and developmentally programmed as well as activity-dependent remodeling of neuronal projections. In addition, like neurons, glial cells are integral to both formation and function of the brain. To elucidate the molecular mechanisms governing brain development, we propose to continue studying post-embryonic development of the Drosophila brain that involves various interesting developmental phenomena, such as extensive neurogenesis and gliogenesis in functional neural circuits and large-scale remodeling of neural circuits during metamorphosis. First, we will identify additional molecules required for various aspects of post-embryonic development of the Drosophila brain via isolating and characterizing more mushroom body mutants. Second, we will investigate whether and how numerous distinct DSCAM molecules operate collaboratively and/or differentially to mediate diverse cell type-specific neuronal morphogenesis. Third, we will develop novel MARCM technology for examining post-embryonic neurogenesis and gliogenesis systematically and simultaneously. Studying post-embryonic development of the Drosophila brain promises to shed new light on how complex neural circuits form in human brains. In particular, we expect to gain novel insights into the molecular mechanisms that govern (1) derivation of different types of neurons from common precursors, (2) chronologically appropriate neuronal morphogenesis, (3) formation/extension/guidance/arborization of dendrites versus axons, (4) remodeling of neuronal projections, (5) diverse cell type-specific neuronal morphogenesis, and (6) neuron-glial interactions.

描述（由申请人提供）：大脑发育涉及不同类型神经元的有序生成，刻板神经元连接的建立，以及神经元投射的发育程序化和活动依赖性重塑。此外，像神经元一样，神经胶质细胞对大脑的形成和功能都是不可或缺的。为了阐明控制大脑发育的分子机制，我们建议继续研究果蝇大脑的胚胎后发育，包括各种有趣的发育现象，如功能神经回路中广泛的神经发生和胶质发生，以及变态过程中神经回路的大规模重塑。首先，我们将通过分离和表征更多的蘑菇体突变体来确定果蝇大脑胚胎后发育各个方面所需的额外分子。其次，我们将研究众多不同的DSCAM分子是否以及如何协同和/或差异地介导多种细胞类型特异性神经元形态发生。第三，我们将开发新的MARCM技术，系统地同时检测胚胎后神经发生和胶质瘤发生。研究果蝇大脑的胚胎后发育有望揭示复杂的神经回路是如何在人类大脑中形成的。特别是，我们期望对以下分子机制获得新的见解：(1)从共同前体衍生出不同类型的神经元，(2)按时间顺序适当的神经元形态发生，(3)树突与轴突的形成/延伸/引导/树突化，(4)神经元投射的重塑，(5)不同细胞类型特异性的神经元形态发生，以及(6)神经元-胶质相互作用。