Transcriptional regulation of post-embryonic neuronal maturation

胚胎后神经元成熟的转录调控

• 批准号: 10470423
• 负责人: Haosheng Sun
• 金额: $ 24.9万
• 依托单位: UNIVERSITY OF ALABAMA AT BIRMINGHAM
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-09-30 至 2024-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10470423
• 关键词: ATAC-seq; Acute; Address; Adolescent; Adult; Affect; Afferent Neurons; Award; Behavioral; Bioinformatics; Brain; Caenorhabditis elegans; Cell Nucleus; Chromatin; Chronic; Complex; Data; Data Set; Development; Disease; Electrophysiology (science); Embryo; Environment; Environmental Risk Factor; Etiology; Event; Future; Gene Expression Regulation; Genes; Genetic; Genetic Risk; Genetic Screening; Genetic Transcription; Genomics; Goals; Human; Impairment; Individual; Intellectual functioning disability; Interneurons; Knowledge; Laboratories; Lead; Life; Mentorship; Methods; MicroRNAs; Mitotic; Molecular; Morphology; Nematoda; Nervous system structure; Neurodevelopmental Disorder; Neurons; Neurosciences Research; Neurotransmitters; Organism; Pathway interactions; Phase; Physiology; Positioning Attribute; Post-Transcriptional Regulation; Postdoctoral Fellow; Poverty; Predisposition; Preparation; Primates; Process; Publishing; Regulation; Regulator Genes; Reporter Genes; Research; Research Personnel; Research Proposals; Resolution; Role; Sensory; Specific qualifier value; Specificity; Stereotyping; Stimulus; Structure; Synapses; System; Temperature; Testing; The Sun; Training; Transcriptional Regulation; Universities; Work; autism spectrum disorder; axon guidance; behavioral plasticity; bioinformatics tool; brain tissue; design; experimental study; improved; insight; migration; mutant; nervous system development; neurodevelopment; neurotechnology; new therapeutic target; novel; perinatal period; post-doctoral training; postnatal development; postnatal period; programs; relating to nervous system; skills; synaptogenesis; tool; transcription factor; transcriptome; transcriptome sequencing; transcriptomics; young adult

PROJECT SUMMARY/ABSTRACT During the complex and intricately-timed sequence of nervous system development and maturation, significant and persistent disruptions to the dynamic regulatory process through genetic and environmental risks can result in neurodevelopmental disorders. Neuroscience research has contributed much to our understanding of early neural development in the embryonic and perinatal periods including neuronal specification, neuronal migration, axonal guidance/outgrowth, and synaptogenesis. The period from early post-natal life to young adulthood is equally critical for proper development of the mature brain, as extensive structural and behavioral plasticity are observed during these periods. However, much less is known about the molecular regulatory mechanisms underlying neuronal maturation during post-natal development. In the first part of my post-doctoral work, I developed and optimized a method to isolate single neuron types for genomics profiling. Using this method, in combination with the genetic amenability of the C. elegans system, I will profile the transcriptome and chromatin accessibility of single neuron types throughout early post-natal development to young adulthood (Aim 1). In Aim 2, using the profiling data from Aim 1 as an entry point, I will take a 2-pronged approach to identify novel regulators of neuronal maturation. First, I will co-develop and implement bioinformatics tools to extract common cis-regulatory motifs from developmentally regulated genes and predict candidate transcriptional regulators. Second, using validated developmentally-regulated gene reporters in Aim 1, I will conduct unbiased forward genetic screens to identify novel regulators of neuronal maturation. In Aim 3, I will use advanced neurotechnology tools to examine the role of environmental stimuli (sensory-induced neuron activity) on neuronal maturation. First, I will examine how acute and chronic inhibition of activity in target neurons, during different developmental windows, affects single-neuron developmental transcriptomes and chromatin accessibility. In addition, the interaction between pathways regulating neuronal maturation through environmentally-induced activity versus intrinsic genetic mechanisms will be examined using approaches as in Aim 2. The proposed research will increase our understanding of the genetic and environmental regulatory mechanisms underlying normal post-natal neurodevelopment, improve our understanding of the etiology of neurodevelopmental disorders, and reveal novel therapeutic targets. The training phase of the award, conducted in the laboratory of Dr. Oliver Hobert and under the co- mentorship of Dr. Harmen Bussemaker and Dr. Stavros Lomvardas at Columbia University, outlines a comprehensive plan for the acquisition of technical and professional skills that will enable my transition to an independent research position. The successful completion of this project will provide a platform for future experiments aimed at understanding gene-environment interplay in the transcriptional regulation of nervous system development and function. .

项目总结/摘要 在神经系统发育和成熟的复杂和错综复杂的时间序列中， 通过遗传和环境的动态调节过程的重大和持续的干扰 风险可能导致神经发育障碍。神经科学研究对我们的 了解胚胎和围产期的早期神经发育，包括神经元 特异性、神经元迁移、轴突引导/生长和突触发生。从早期的时期 出生后的生活到年轻的成年期对于成熟大脑的适当发育同样重要， 在这些时期观察到结构和行为的可塑性。然而，人们对它的了解要少得多。 出生后发育过程中神经元成熟的分子调控机制。上 作为博士后工作的一部分，我开发并优化了一种分离基因组学中单个神经元类型的方法 侧写利用该方法，结合C. elegans系统，我会 在整个出生后早期描绘单个神经元类型的转录组和染色质可及性 1、青年期（Aim 1）。在目标2中，使用来自目标1的剖析数据作为切入点， 将采取双管齐下的方法来识别神经元成熟的新调节因子。首先，我将共同开发和 应用生物信息学工具从发育调控基因中提取共同顺式调控基序 并预测候选转录调节因子。第二，使用经过验证的发育调控基因 在目标1中，我将进行无偏的正向遗传筛选，以确定神经元的新调节因子。 成熟在目标3中，我将使用先进的神经技术工具来研究环境刺激的作用 （感觉诱导的神经元活动）对神经元成熟的影响。首先，我将研究急性和慢性抑制 在不同的发育窗期，靶神经元的活动影响单个神经元的发育， 转录组和染色质可及性。此外，调节神经元的通路之间的相互作用 通过环境诱导的活动与内在遗传机制的成熟将被检查 使用目标2中的方法。这项拟议中的研究将增加我们对遗传和 环境调节机制的基础正常出生后的神经发育，提高我们的 了解神经发育障碍的病因，并揭示新的治疗靶点。 该奖项的培训阶段，在奥利弗霍伯特博士的实验室进行，并根据共同的， Harmen Bussemaker博士和Stavros Lomvardas博士在哥伦比亚大学的指导，概述了一个 全面的计划，以获得技术和专业技能，使我能够过渡到一个 独立研究立场。该项目的成功完成将为未来的 实验旨在了解基因环境相互作用的转录调节神经 系统开发和功能。 .