Control of the 4D chromatin landscape underlying gene activity during development

发育过程中基因活性的 4D 染色质景观控制

• 批准号: 10265595
• 负责人: Thomas Gregor
• 金额: $ 64.62万
• 依托单位: PRINCETON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-17 至 2025-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10265595
• 关键词: 3-Dimensional; Acute; Address; Alleles; Animals; Architecture; Biological; Biological Assay; Biological Models; Biology; Boundary Elements; Cell Line; Cell Nucleus; Cells; Cellular biology; Characteristics; Chromatin; Chromosome Structures; Chromosomes; Complex; Crowding; Cues; Defect; Development; Developmental Biology; Developmental Process; Disease; Drosophila genus; Embryo; Engineering; Enhancers; Environment; Event; Gene Expression; Genes; Genetic; Genetic Transcription; Genome; Genomics; Goals; Homeobox Genes; Homeostasis; Image; Individual; Kinetics; Light; Link; Liquid substance; Malignant Neoplasms; Mammalian Cell; Mammals; Measurement; Measures; Membrane; Methods; Modeling; Modernization; Molecular Conformation; Monitor; Mus; Nuclear; Organoids; Output; Pattern; Phase; Physical condensation; Play; Population; Process; Proteins; Regulator Genes; Regulatory Element; Reporter; Resolution; Role; Stochastic Processes; System; Techniques; Technology; Testing; Time; Tissues; Transcription Coactivator; Transcriptional Regulation; Visualization; cell fate specification; cell type; cohesin; cohesion; developmental disease; embryonic stem cell; fly; functional gain; gastrulation; genetic manipulation; genome-wide; genomic locus; high resolution imaging; imaging modality; implantation; in vivo; novel; novel strategies; optogenetics; programs; promoter; public health relevance; response; spatiotemporal; tool; transcription factor; whole genome

Summary One of the grand challenges of modern biology is to understand how gene activity is controlled in space and time, in the context of native chromosomes and in individual living cells. The goal of this proposal is to tackle exactly this challenge: we will develop new approaches to measure and manipulate long-range chromosomal interactions and quantify their effects on gene expression, in real-time and in living cells and tissues. By quantitatively mapping the relationship between transcription factor assembly (e.g. formation of biomolecular condensates), chromosome organization and transcription kinetics, our study will define how gene expression is controlled at unprecedented resolution. Transcriptional regulation forms the basis of cellular differentiation during organismal development, and its defects underlie a variety of disease states, from developmental disorders to cancer. Yet current methods are limited: traditional live-imaging lacks the spatial resolution to accurately define chromosome organization at the scale of individual genes, while bulk assays using fixed material are ill-suited for studying temporal dynamics. In addition, membrane-less nuclear condensates, which form through liquid-liquid phase separation, are thought to play key but as-yet-undefined roles in regulating transcription. To address these challenges, we will develop new imaging methods to measure chromosomal distances in living cells and build optogenetic tools to assemble/disassemble chromosome loops and nuclear condensates. We will deploy these tools to examine regulatory interactions at genomic scales characteristic of enhancer– promoter interactions in flies and mammals (from tens to hundreds of kilobases), and study their implications in the context of cell fate specification in the developing Drosophila embryo. The resulting technologies will be applied to analogous transcriptional loci in mouse embryonic stem cells and organoids derived from these cells. Together, the proposed studies will help reveal how robust mechanisms of cell type specification emerge from stochastic processes such as transcriptional bursts, fluctuations in the size and stability of biomolecular condensates, and dynamic instability of chromatin architecture. The overall goal of this project is to establish a quantitative link between chromatin architecture and transcriptional activity, which will ultimately allow us to take control of gene activity by re-engineering the transcriptional programs underlying developmental and disease processes.

总结 现代生物学的重大挑战之一是了解基因活动如何在太空中控制， 时间，在自然染色体和个体活细胞的背景下。该提案的目的是解决 我们将开发新的方法来测量和操纵长距离染色体， 实时和在活细胞和组织中进行相互作用并量化其对基因表达的影响。通过 定量绘制转录因子组装（例如生物分子的形成）之间的关系 浓缩物），染色体组织和转录动力学，我们的研究将定义基因表达是如何被激活的。 以前所未有的分辨率进行控制。 转录调控是生物体发育过程中细胞分化的基础， 缺陷是从发育障碍到癌症的各种疾病状态的基础。然而，目前的方法是 限制：传统的实时成像缺乏空间分辨率，无法准确定义染色体的组织结构。 单个基因的规模，而使用固定材料的批量测定不适合研究时间动态。在 此外，通过液-液相分离形成的无膜核冷凝物被认为 在调节转录中起着关键但尚未确定的作用。 为了应对这些挑战，我们将开发新的成像方法来测量染色体距离， 活细胞和构建光遗传学工具来组装/拆卸染色体环和核浓缩物。 我们将部署这些工具来研究增强子特征的基因组尺度上的调控相互作用， 启动子相互作用在苍蝇和哺乳动物（从几十到几百个酶），并研究其影响， 果蝇胚胎发育过程中细胞命运特化的背景。由此产生的技术将是 应用于小鼠胚胎干细胞和衍生自这些细胞的类器官中的类似转录位点。 总之，拟议的研究将有助于揭示细胞类型特化的强大机制是如何出现的， 随机过程，如转录爆发，生物分子大小和稳定性的波动， 浓缩物和染色质结构的动态不稳定性。该项目的总体目标是建立一个 染色质结构和转录活性之间的定量联系，这将最终使我们能够 通过重新设计发育和疾病的转录程序来控制基因活性 流程.