New modes and mechanisms of negative regulation of LIN-12/Notch in C. elegans

线虫中LIN-12/Notch负调控的新模式和新机制

• 批准号: 9296137
• 负责人: Iva S Greenwald
• 金额: $ 34万
• 依托单位: COLUMBIA UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-09-21 至 2019-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9296137
• 关键词: Address; Adopted; Aging; Animals; Binding; Biochemical; Biological Assay; Caenorhabditis elegans; Cancer Etiology; Cancer Patient; Candidate Disease Gene; Cell Communication; Cell Culture Techniques; Cells; Complex; Development; Diagnostic; Disease; Down-Regulation; Endocytosis; Ensure; Environment; Epidermal Growth Factor Receptor; Experimental Designs; Feedback; Gene Targeting; Genes; Genetic; Goals; Health; Homeostasis; Human; Human Development; Image; Immune System Diseases; Individual; Injury; Insulin; Knowledge; Larva; Lead; Ligands; Lobular Neoplasia; Malignant Neoplasms; Mammalian Cell; Mediating; Membrane; Mission; Mutate; Mutation; Mutation Analysis; Nuclear; Oncogenes; Oncogenic; Pathway interactions; Pattern; Phosphotransferases; Physiology; Positioning Attribute; Property; RNA interference screen; Receptor Activation; Refractory; Regulation; Reporter Genes; Resistance; Role; Route; Signal Pathway; Signal Transduction; Somatomedins; Spottings; Stem cells; Surface; Syndrome; System; Tertiary Protein Structure; Textbooks; Therapeutic; Time; Tissues; Trans-Activators; Transgenes; Tumor Suppressor Proteins; United States National Institutes of Health; Work; cell fate specification; chemotherapy; developmental disease; gene discovery; genetic analysis; human disease; in vivo; in vivo imaging; insight; multipotent cell; mutant; nervous system disorder; notch protein; novel strategies; precursor cell; prevent; public health relevance; receptor; response; stem-like cell; tool; trafficking; transcription factor; transcriptomics

 DESCRIPTION (provided by applicant): The overall goal of this application is to elucidate different mechanisms for negative regulation of Notch signaling. Notch is the eponymous receptor in a major signaling system for cell-cell interactions and cell fate specification in animl development. Regulating Notch signaling appropriately--in space, time, strength or duration--is critically important for normal development. Furthermore, aberrant Notch activity has been implicated in many different cancers, as well as in developmental, immune, and neurological disorders. Thus, the proposed work has many implications for human health. The deeper understanding of developmental mechanism has great potential for developing diagnostic and therapeutic tools for human disease, a central mission of the NIH. Our past work on LIN-12/Notch signaling in C. elegans has afforded many fundamental insights into conserved roles, mechanisms, and regulation of Notch signaling. We expect that our continued work in this system will continue to reveal mechanisms of general relevance, and particular aspects of experimental design were chosen to maximize this prospect. Each aim of this application explores different ways LIN-12/Notch activity and stability is modulated in a textbook developmental paradigm in which six multipotential precursor cells adopt one of three distinct fates through LIN-12/Notch-mediated cell-cell interactions. The patterning is precise and robust, reflecting tight spatial and temporal control of LIN-12/Notch activity and multiple modes for integrating LIN-12/Notch activity with other conserved signaling pathways. In Aim 1, we propose to characterize new kinases we identified in a targeted screen for negative regulators and another gene, first identified by a mutation in a cancer patient, we showed acts as a negative regulator in C. elegans. To assess their functional conservation in Notch regulation, we will perform a human cell assay. In Aim 2, we propose to investigate LIN-12/Notch endocytic trafficking and its negative regulation by EGF Receptor activity in developmental patterning. EGF Receptor, like Notch, is an important oncogene, and crosstalk between these pathways occurs in cancer as well as in normal development. In Aim 3, we propose to elucidate how activated nuclear LIN-12/Notch is inhibited by EGF receptor during developmental patterning and by Insulin/Insulin-like Signaling during quiescence in response to unfavorable environment. Quiescence is a fundamental property of critical importance for human health, allowing stem cells to persist over prolonged periods in a competent state so as to be available to repopulate tissues when cells are lost to aging, injury or disease, and for cancer, quiescent stem-like cells are believed to be resistant to standard chemotherapy. Together, these aims will provide much new information about negative regulation of a fundamental signaling pathway in development and disease, in accord with the mission of the NIH.

 说明（由申请人提供）：本申请的总体目标是阐明Notch信号负调控的不同机制。Notch是动物发育中细胞间相互作用和细胞命运特化的主要信号系统中的表观受体。适当地调节Notch信号-在空间，时间，强度或持续时间-对正常发育至关重要。此外，异常的Notch活性与许多不同的癌症以及发育、免疫和神经障碍有关。因此，拟议的工作对人类健康有许多影响。对发育机制的深入理解对于开发人类疾病的诊断和治疗工具具有巨大的潜力，这是NIH的中心使命。 我们过去在C. elegans提供了许多关于Notch信号转导的保守作用、机制和调节的基本见解。我们期望我们在这个系统中的持续工作将继续揭示普遍相关的机制，并且选择实验设计的特定方面来最大化这一前景。本申请的每个目的都探索了在教科书发育范例中调节LIN-12/Notch活性和稳定性的不同方式，其中六种多能前体细胞通过LIN-12/Notch介导的细胞-细胞相互作用采用三种不同命运之一。该模式是精确和稳健的，反映了LIN-12/Notch活性的紧密空间和时间控制以及用于将LIN-12/Notch活性与其他保守信号传导途径整合的多种模式。 在目标1中，我们提出表征我们在针对负调节因子的靶向筛选中鉴定的新激酶和另一个基因，该基因首先通过癌症患者中的突变鉴定，我们显示其在C中作为负调节因子。优美的为了评估它们在Notch调节中的功能保守性，我们将进行人细胞测定。目的2：研究LIN-12/Notch内吞转运及其在发育模式中受EGF受体活性的负调控。与Notch一样，EGF受体是一种重要的致癌基因，这些途径之间的串扰发生在癌症和正常发育中。在目标3中，我们建议阐明如何激活核LIN-12/Notch是抑制EGF受体在发育模式和胰岛素/胰岛素样信号在静止期响应不利的环境。静止是对人类健康至关重要的基本性质，允许干细胞在有能力的状态下持续较长时间，以便当细胞因衰老、损伤或疾病而丢失时可用于重新填充组织，并且对于癌症，静止的干细胞样细胞被认为对标准化疗具有抗性。总之，这些目标将提供许多关于发育和疾病中基本信号通路负调控的新信息，与NIH的使命保持雅阁。