Homeobox Gene Six3 in Forebrain and Visual System Development

同源盒基因 Six3 在前脑和视觉系统发育中的作用

• 批准号: 7998167
• 负责人: GUILLERMO C OLIVER
• 金额: $ 39.92万
• 依托单位: ST. JUDE CHILDREN'S RESEARCH HOSPITAL
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-03-01 至 2012-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7998167
• 关键词: Address; Animal Model; Anterior; Biological Assay; Biotinylation; Brain; Collection; Complex; Critiques; Development; Elements; Eye; Forebrain Development; Genes; Genetic; Genomics; Goals; Homeobox Genes; Lens Placodes; Molecular; Molecular Profiling; Mutation; Neuraxis; Pathway interactions; Pattern; Phase; Process; Prosencephalon; Publications; Regulatory Pathway; Research Design; Retina; Role; Structure; Telencephalon; diencephalon; embryonic stem cell; in vivo; information gathering; lens; neural plate; novel; promoter; research study; tool; vision development

DESCRIPTION (provided by applicant): The forebrain is the most anterior portion of the central nervous system and gives rises to the telencephalon, diencephalon, and the eyes during development. All derivatives of the forebrain originate from the anterior neural plate. Therefore, mutations in genes that disrupt forebrain development provide a powerful tool for dissecting the mechanisms that regionalize the neural plate, establish fate restrictions, and determine the identities of all its main derivatives. We have demonstrated that the restricted pattern of Six3 expression is of functional relevance as its activity is essential for vertebrate forebrain, lens and retina development. The goal of this proposal is to continue with the systematic identification and characterization of the functional roles of Six3 during forebrain and visual system development as a tool to help us unravel the cellular and molecular mechanisms participating in the genesis of these structures. During the last few years we have generated an invaluable collection of animal models and molecular tools that are a great asset in the accomplishment of the proposed goals. To this end, we propose to continue using Six3 as an entry point to better characterize its functional role in the development of different brain structures and retina differentiation and lamination.

描述（由申请人提供）：前脑是中枢神经系统的最前部，在发育过程中发育成端脑、间脑和眼睛。前脑的所有衍生物都起源于前神经板。因此，破坏前脑发育的基因突变提供了一个强大的工具，用于解剖神经板区域化的机制，建立命运限制，并确定其所有主要衍生物的身份。我们已经证明Six3表达的限制模式具有功能相关性，因为其活性对于脊椎动物前脑、透镜和视网膜发育是必不可少的。该提案的目标是继续系统地识别和表征Six3在前脑和视觉系统发育过程中的功能作用，作为帮助我们解开参与这些结构发生的细胞和分子机制的工具。在过去的几年里，我们已经产生了动物模型和分子工具，这是一个伟大的资产，在实现拟议的目标的宝贵集合。为此，我们建议继续使用Six3作为切入点，以更好地表征其在不同大脑结构和视网膜分化和分层发育中的功能作用。