Chemical control of protein stability to analyze germline cell fate

化学控制蛋白质稳定性以分析生殖细胞命运

• 批准号: 8121411
• 负责人: Jamie M Verheyden
• 金额: $ 4.63万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-01-01 至 2012-10-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8121411
• 关键词: Animal Genetics; Biological Models; Caenorhabditis elegans; Cell Differentiation process; Cell Maintenance; Cell Proliferation; Cell division; Cells; Chemicals; Chimeric Proteins; Differentiation and Growth; Disease; Equilibrium; Exhibits; Fusion Protein Expression; Genes; Genetic; Germ Cells; Germ Lines; Growth; Health; Investigation; Lead; Malignant Neoplasms; Mammals; Meiosis; Methods; Mitotic; Modeling; Molecular; Oocytes; Phase; Preclinical Drug Evaluation; Proteins; RNA; RNA-Binding Proteins; Regulation; Research Design; Signal Transduction; Stem cells; System; Technology; Tissues; Transgenes; Transgenic Organisms; Undifferentiated; Work; anticancer research; cell growth; glucagon-like peptide 1; in vivo; insight; interest; new technology; notch protein; protein function; self-renewal; small molecule; sperm cell; stem cell differentiation; tumor progression

DESCRIPTION (provided by applicant): The Caenorhabditis elegans (C. elegans) germ line provides a model for the investigation of molecular controls regulating stem cell maintenance and differentiation into sperm or oocyte. Both GLP-1/Notches signaling as well as FBF/PUF RNA binding proteins contribute to maintain stem cells and promote mitotic cell division. FOG-1/CPEB and FOG-3/Tob proteins regulate the specification of germ cells into sperm. Vertebrate Tob has been suggested to be both a transcriptional regulator as well as an RNA regulator with antiproliferative activity. However, the mechanism by which Tob proteins function is poorly understood. These key regulators are part of a network of genes involved in cellular proliferation, stem cell maintenance and differentiation. Investigating how these regulators work in a simple model system where key questions can be explored will provide insight into how they may work among their conserved vertebrate counterparts. Specific Aims: 1) to develop a chemical method for manipulation of protein stability in C. elegans. 2) To chemically manipulate the presence or absence of key germline stem cell regulators (FOG-3, FBF-1, and LAG-2) and investigate their control of germ cell fate. Study Design: I have applied a new technology to C. elegans for conditionally stabilizing transgenic proteins in vivo. When a Destablization Domain (DD) is fused to a protein of interest, it causes rapid degradation of the fusion protein. However, this fusion protein can be stabilized and rendered functional when treated with a small molecule called Shield1. By placing transgenes under tissue specific regulatory sequences I will be able to control expression of fusion proteins in a spatial and temporal manner. FOG-3, FBF-1, and LAG-2 are conserved regulators of stem cell differentiation and maintenance, respectively, and I plan to use this technology to answer key questions about their function in the germ line that have not been possible with existing approaches. Health Relevance: These studies will contribute to our understanding of the regulation of stem cell maintenance and differentiation. Since the regulation of germ line stem cell maintenance involves genetic regulators which are conserved form C. elegans to mammals, our studies will help to uncover details of how these genes govern stem cell growth and keep them in an undifferentiated state. Investigating the basic components that keep cells in a mitotic growth phase versus causing them to differentiate is essential in our understanding of cancer progression and methods of treatment.

描述（由申请人提供）：秀丽隐杆线虫（C. elegans）生殖系为研究调节干细胞维持和分化成精子或卵母细胞的分子控制提供了模型。GLP-1/Notches信号传导以及FBF/PUF RNA结合蛋白都有助于维持干细胞并促进有丝分裂细胞分裂。FOG-1/CPEB和FOG-3/Tob蛋白调节生殖细胞向精子的特化。脊椎动物Tob被认为是一种转录调节因子，也是一种具有抗增殖活性的RNA调节因子。然而，Tob蛋白的功能机制知之甚少。这些关键调节因子是参与细胞增殖、干细胞维持和分化的基因网络的一部分。研究这些调节器如何在一个简单的模型系统中工作，其中可以探索关键问题，将提供深入了解它们如何在保守的脊椎动物中工作。具体目的：1）建立一种化学方法来控制C.优雅的2)以化学方式操纵关键生殖系干细胞调节因子（FOG-3、FBF-1和LAG-2）的存在或不存在，并研究其对生殖细胞命运的控制。研究设计：我将一项新技术应用于C语言。用于在体内条件稳定转基因蛋白质。当去稳定化结构域（DD）与目的蛋白融合时，其引起融合蛋白的快速降解。然而，这种融合蛋白可以被稳定，并赋予功能时，用一个小分子称为盾牌1处理。通过将转基因置于组织特异性调控序列下，我将能够以空间和时间的方式控制融合蛋白的表达。FOG-3、FBF-1和LAG-2分别是干细胞分化和维持的保守调节因子，我计划使用这项技术来回答有关它们在生殖系中功能的关键问题，这些问题是现有方法无法解决的。健康相关性：这些研究将有助于我们理解干细胞维持和分化的调节。由于生殖系干细胞维持的调控涉及保守的C型遗传调节因子。从线虫到哺乳动物，我们的研究将有助于揭示这些基因如何控制干细胞生长并使其保持在未分化状态的细节。研究使细胞保持在有丝分裂生长阶段的基本成分，而不是使它们分化，对于我们理解癌症进展和治疗方法至关重要。