EGG TO EMBRYO--GENE REGULATORY CIRCUITRY IN DEVELOPMENT

卵子到胚胎——发育中的基因调控电路

• 批准号: 6388029
• 负责人: ERIC H DAVIDSON
• 金额: $ 107.08万
• 依托单位: CALIFORNIA INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-04-01 至 2004-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6388029
• 关键词: developmental genetics; early embryonic stage; genetic regulatory element; invertebrate embryology; transcription factor

The focus of research in the three laboratories that constitute this Program Project is the molecular basis of regulatory flow in early embryonic development. The Program Project will utilize the highly developed sea urchin and ascidian model systems for this research. Major objective are to develop functional comprehension of cis-regulatory systems that control genes expressed spatially in the early embryo, using genes that operate at different levels of the gene regulatory network; to discern the overall architecture of this network; and to discern the molecular mechanisms by which maternal transcription factors are activated, and control is transformed from maternal to zygotic regulatory processes. The three Research Components are:(1) Davidson Component, "Gene Regulatory Mechanisms and the Control of Early Embryogenesis"; (2) Fraser Component, "In Vivo Imaging of Gene Regulatory Events in the Early Embryo"; (3) Levine Component "Gene Regulation in the Ascidian Ciona intestinalis." The major aims of the Davidson Component are cis-regulatory analysis of genes expressed differentially in the sea urchin embryo, and identification and characterization of the maternal and zygotic transcription factors which control this expression. The major focus of the Fraser Component is visualization of the state of cis-regulatory elements in vivo and spatial visualization by new imaging methods of modifications of maternal transcription factors, using experimental systems characterized in the Davidson Component. The major focus of the Levine Component will be cis-regulatory analysis of certain key regulatory genes expressed in ascidian embryos, which are also to be characterized in the sea urchin embryo in the Davidson Component, and interphyletic gene transfer experiments to be carried out collaboratively between the Davidson and Levine labs. A salient characteristic of the proposed research is the engagement of powerful new technologies, some entirely novel. All the Components. Will rely on two Research Core Facilities, viz the SUMS Facility at Caltech's Marine Laboratory, which will provide sea urchins, gametes and nuclear extracts from which transcription factors are purified; and the Microsequencing Facility, where partially purified transcription factors are sequenced at picomole levels. An Administrative Core will oversee management, budget, and interlaboratory communication, with respect to material, financial, and intellectual matters.

构成该计划项目的三个实验室的研究重点是早期胚胎发育中调控流的分子基础。该计划项目将利用高度发达的海胆和海鞘模型系统进行这项研究。主要目标是开发顺式调控系统的功能理解，控制基因表达的空间在早期胚胎中，使用基因调控网络的不同水平上运作的基因;辨别这个网络的整体架构;并辨别的分子机制，其中母体转录因子被激活，控制从母体到合子的监管过程。三个研究部分是：（1）Davidson部分，“基因调控机制和早期胚胎发生的控制”;（2）Fraser部分，“早期胚胎中基因调控事件的体内成像”;（3）Levine部分，“海鞘中的基因调控”。Davidson组件的主要目的是对海胆胚胎中差异表达的基因进行顺式调控分析，并鉴定和表征控制这种表达的母体和合子转录因子。弗雷泽组件的主要重点是可视化的顺式调控元件在体内的状态和空间可视化的新成像方法的修改母体转录因子，使用实验系统的特点戴维森组件。Levine组件的主要重点将是对海鞘胚胎中表达的某些关键调控基因进行顺式调控分析，这些基因也将在Davidson组件的海胆胚胎中进行表征，以及Davidson和Levine实验室之间合作进行的系间基因转移实验。拟议研究的一个显著特点是采用了强大的新技术，其中一些是全新的。所有组件。将依靠两个研究核心设施，即加州理工学院海洋实验室的SUMS设施，该设施将提供海胆，配子和核提取物，从中纯化转录因子;和微测序设施，部分纯化的转录因子在皮摩尔水平上测序。一个行政核心将监督管理、预算和实验室间的沟通，涉及材料、财务和知识事项。