Investigating progenitor cell development and lineage relationships in the brain

研究大脑中祖细胞的发育和谱系关系

• 批准号: 10414351
• 负责人: Bushra Raj
• 金额: $ 24.9万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-07-01 至 2024-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10414351
• 关键词: Address; Advisory Committees; Algorithms; Animal Model; Award; Bar Codes; Behavior; Bioinformatics; Brain; Brain region; CRISPR/Cas technology; Cell Lineage; Cell division; Cells; Chromatin; Code; Competence; Core Facility; Data; Data Set; Development; Developmental Biology; Disease model; Embryo; Enhancers; Feedback; Gene Expression; Gene Expression Profile; Genetic; Genetic Transcription; Genomics; Goals; Grant; Maps; Memory; Mentors; Mentorship; Methods; Modeling; Molecular; Molecular and Cellular Biology; Natural regeneration; Neurobiology; Neurodevelopmental Disorder; Neuroglia; Neurons; Neurotransmitters; Organoids; Pathway interactions; Population; Process; Proliferating; Radial; Recording of previous events; Regulator Genes; Regulatory Element; Research; Resolution; Resources; Role; Running; Specific qualifier value; Stem Cell Development; Study models; Technology; Time; To specify; Training; Trees; Type I Epithelial Receptor Cell; Vision; Writing; Zebrafish; analytical method; base; career; cell fate specification; cell type; experience; genome resource; genome-wide; graduate student; imprint; insight; mathematical model; meetings; member; nerve stem cell; neurodevelopment; neurogenesis; progenitor; programs; reconstruction; relating to nervous system; segregation; single cell analysis; single-cell RNA sequencing; tool; transcriptome; transcriptomics; translational approach; zebrafish development

PROJECT SUMMARY/ABSTRACT A key goal in developmental biology is to understand how the brain is specified and organized regionally, cellularly and molecularly. Central to this vision is determining the origins and fates of cells during development, and thus map the progressive steps of cell specification and lineage divergences. Focused efforts have provided insight into specific cell types and lineages, however global views of these processes have been lacking. Recent technological breakthroughs in single-cell transcriptomics and lineage tracing using CRISPR-Cas9 tools are now enabling the realization of this vision. The long-term goal of this project is to obtain global views of cellular relationships and molecular changes during neural development and cell type diversification in the vertebrate brain. These include generating large-scale, single-cell resolution cell specification trajectories that describe molecular cascades underlying cell fate specification (Aim 1), and lineage trees that describe the history of cell divisions (Aim 2). These trees represent many key aspects of developmental decisions and can be used to determine gene expression cascades during cell specification and regulatory factors involved in progenitor priming and neuron identity (Aim 1). Furthermore, they can address how often transcriptional and lineage identities are related (Aim 2). These studies will generate resources for genome-wide and single-cell analysis of brain development and reveal cellular and molecular mechanisms for generating neuronal cell diversity. My career goal is to run an academic lab aimed at investigating cellular and molecular features underlying brain development, neurogenesis and neural stem cell activity using global and focused approaches. The proposed research draws on my previous experience with characterizing gene regulatory networks in neurogenesis and extends it to a new model organism, zebrafish, while exposing me to new experimental and analytical methods. I have developed a detailed training plan with my co-mentors, Drs. Len Zon, Alex Schier, and Josh Sanes, who have combined expertise in development, behavior, neurobiology, single-cell analysis and disease modeling. To help me transition to independence, we will meet regularly to discuss research progress, brainstorm ideas, and obtain guidance on grant writing, mentorship and lab management. My K99 advisory committee consists of Drs. Allon Klein, Sean Megason and Gord Fishell, whose collective expertise in single-cell genomics, zebrafish development, and neurobiology will provide me with technical and conceptual feedback in executing my research plan. I will continue to mentor a research technician/graduate student, will present my research at two meetings per year, take courses on bioinformatic analysis, mathematical modeling and grant writing, and attend seminars to broaden my scientific training. As a member of the Harvard Department of Molecular and Cellular Biology, I will have access to leaders in developmental biology, neurobiology and genetics, as well as cutting-edge core facilities. The Pathway to Independence Award will provide me with resources to initiate an ambitious research program and obtain additional training to maximize my chances of a successful transition to independence.

项目总结/摘要 发育生物学的一个关键目标是了解大脑是如何在区域上被指定和组织的， 细胞和分子上。这一愿景的核心是确定细胞在发育过程中的起源和命运， 从而绘制出细胞特化和谱系分化的渐进步骤。重点工作提供了 然而，对这些过程缺乏全面的看法。最近 现在，使用CRISPR-Cas9工具在单细胞转录组学和谱系追踪方面的技术突破， 使这一愿景得以实现。该项目的长期目标是获得全球的细胞 脊椎动物神经发育和细胞类型多样化过程中的关系和分子变化 个脑袋这些包括生成大规模的单细胞分辨率细胞规格轨迹， 细胞命运特化的分子级联（Aim 1）和描述细胞历史的谱系树 （目标2）。这些树代表了发展决策的许多关键方面，可用于 确定细胞特化过程中的基因表达级联以及参与祖细胞分化的调节因子 启动和神经元身份（目标1）。此外，他们可以解决转录和谱系 身份是相关的（目标2）。这些研究将为全基因组和单细胞分析提供资源， 大脑发育和揭示产生神经元细胞多样性的细胞和分子机制。 我的职业目标是管理一个学术实验室，旨在研究大脑的细胞和分子特征。 发展，神经发生和神经干细胞的活动，使用全球和重点的方法。拟议 研究借鉴了我以前在神经发生中表征基因调控网络的经验， 将其扩展到一种新的模式生物，斑马鱼，同时让我接触到新的实验和分析方法。 我和我的导师Len Zon博士、Alex希耶博士和Josh Sanes博士一起制定了一个详细的培训计划， 结合了发育、行为、神经生物学、单细胞分析和疾病建模方面的专业知识。到 帮助我过渡到独立，我们将定期开会讨论研究进展，集思广益， 获得有关资助撰写、指导和实验室管理的指导。K99咨询委员会由博士组成。 Allon Klein，Sean Megason和Gord Fishell，他们在单细胞基因组学，斑马鱼 发展，神经生物学将为我提供技术和概念上的反馈，在执行我的研究 计划我将继续指导研究技术员/研究生，将在两次会议上介绍我的研究 每年，参加生物信息学分析，数学建模和赠款写作课程，并参加研讨会 拓宽我的科学训练作为哈佛分子和细胞生物学系的一员，我 将有机会接触到发育生物学、神经生物学和遗传学领域的领导者， 设施独立之路奖将为我提供资源，以启动一项雄心勃勃的研究 计划并获得额外的培训，以最大限度地提高我成功过渡到独立的机会。