Development of Genetic Tools for a Short-lived Fish Model in Aging Research

衰老研究中短寿命鱼类模型遗传工具的开发

• 批准号: 8301160
• 负责人: CUNMING DUAN
• 金额: $ 22.8万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-04-01 至 2014-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8301160
• 关键词: Adult; Affinity; Aging; Animal Model; Animals; Binding; Biological Availability; Biology; Biology of Aging; Blood Circulation; Cell Nucleus; Cell Survival; Cells; Communities; Cyprinodontidae; Desiccation; Development; Diagnostic; Endocrine; Engineering; Evolution; Exhibits; Family; Fishes; Fundulus heteroclitus; Gene Expression; Gene Transfer Techniques; Genes; Genetic; Genetic Screening; Genome; Genomics; Goals; Health; In Vitro; Inbreeding; Insulin; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Insulin-Like Growth Factor II; Insulin-Like Growth-Factor-Binding Proteins; Insulin-Like-Growth Factor I Receptor; Investigation; Knock-out; Knowledge; Lead; Life; Ligand Binding; Ligands; Liver; Longevity; Maintenance; Metabolism; Methods; Modeling; Modification; Mus; Nature; Nuclear; Organism; Partner in relationship; Pathway interactions; Play; Positioning Attribute; Proteins; Regulation; Reporter Genes; Research; Research Project Grants; Resources; Role; Seasons; Siblings; Signal Pathway; Signal Transduction; Somatomedins; Somatotropin; Staging; Technology; Testing; Therapeutic; Tissues; Transgenic Organisms; United States; Vertebrates; Zebrafish; Zinc Fingers; aging population; autocrine; base; cell type; cold temperature; cost; egg; experience; fly; gene discovery; genetic analysis; genetic manipulation; insight; interest; loss of function; member; mutant; novel; nuclease; paracrine; receptor; research study; response; teleost fish; tool

DESCRIPTION (provided by applicant): Animals with experimentally manipulable genomes have been invaluable for aging research. In model organisms such as worms, flies, and mice, the ability to specifically add or delete a gene enables the characterization of the roles of specific gene(s) in lifespan regulation. While these animal models have contributed, and will continue to contribute, to our understanding of aging biology, there are gaps in the range of experimental strengths provided by each of the existing animal models. This project will focus on a new and promising vertebrate model organism, the annual turquoise killifish (Nothobranchius furzeri), which has a lifespan of just several months. N. furzeri provides many additional advantages, such as the ability to produce many sibling progeny from a single mating, low cost of maintenance, amenability to forward genetic screens, and the ability of their eggs to be stored dry at low temperatures for as long as a year. Despite these advantages, the N. furzeri model has not been widely used in the field of aging research. This is in part because genetic manipulation experiments were not possible in this species. Recently, my lab has succeeded in developing methods for generating stable and inducible transgenesis in this species. Drawing on our research experience with fish biology and the IGF signaling pathway, the goal of this application is to develop new genetic tools for conducting loss-of-function studie and to use them to test the hypothesis that insulin-like growth factor binding protein-3 (IGFBP-3), a major IGFBP, regulates lifespan via IGF-dependent and/or -independent mechanisms. IGFBP-3 regulates IGF availability by binding IGF tightly and releasing it only under certain conditions. IGFBP-3 also has IGF-independent actions. It is possible that this conserved and multifunctional protein may play key roles in modulating aging. In Aim 1, we will develop genetic tools and use them to determine the role of IGFBP-3 in lifespan regulation. Aim 2 will investigate the functional significance of ligand-binding and nuclear localization of IGFBP-3 by generating and studying inducible transgenic lines that express either wild type or a mutant form of IGFBP-3. The completion of the proposed studies will provide novel insights into the roles of IGFBP-3 in the longevity of vertebrates. The anticipated results will also lead to the development of much needed methods and genetic tools to knockout a gene of interest or to induce gene expression in a tissue-specific and temporally restricted manner in this emerging vertebrate model. The methods and transgenic tools developed in this project will be broadly disseminated and distributed to the scientific community. These genetic tools and methods, combined with the unique features and the extremely short-lifespan of N. furzeri, will open many new avenues for investigations and should facilitate new discoveries in vertebrate aging biology. A better understanding of the biology of aging regulation will likely lead to the development of diagnostic and therapeutic tools that will increase the healthy lifespan of the aging population in the United States. PUBLIC HEALTH RELEVANCE: This project will test the hypothesis that insulin-like growth factor (IGF) binding protein-3, a major IGF binding protein, regulates lifespan via IGF-dependent and/or -independent mechanisms using turquoise killifish, a unique vertebrate that has a lifespan of just several months. This project will also develop new genetic tools, which will make it possible to experimentally manipulate the genome in this new aging biology model. The new genetic tools, combined with the extremely short lifespan and other unique features of this new vertebrate model, should help to facilitate new discoveries in vertebrate aging biology. A better understanding of the roles of IGF signaling in lifespan regulation will likely lead to the development of diagnostic and therapeutic tools that will increase the health of the aging population in the United States.

描述(由申请人提供)：具有可实验操作的基因组的动物对于衰老研究具有无价的价值。在蠕虫、苍蝇和小鼠等模式生物中，特定添加或删除基因的能力使特定基因(S)在寿命调节中的作用得以表征。虽然这些动物模型已经并将继续为我们理解衰老生物学做出贡献，但现有的每个动物模型提供的实验优势范围都存在差距。该项目将专注于一种新的、有前途的脊椎动物模式生物--一年生绿松石龙鱼(Nothobranchius Furzeri)，它的寿命只有几个月。白纹伊蚊提供了许多额外的优势，例如能够从一次交配中产生许多兄弟姐妹后代，维护成本低，易于转发遗传筛选，以及它们的卵子能够在低温下干燥储存长达一年。尽管有这些优点，N.Furzeri模型还没有被广泛应用于衰老研究领域。这在一定程度上是因为基因操纵实验在这个物种中是不可能的。最近，我的实验室成功地开发了在这个物种中产生稳定和可诱导的转基因的方法。借鉴我们在鱼类生物学和IGF信号通路方面的研究经验，这项应用的目标是开发新的遗传工具来进行功能丧失的研究，并用它们来检验胰岛素样生长因子结合蛋白-3(IGFBP-3)是一种主要的IGFBP，通过IGF依赖和/或非依赖的机制来调节寿命。IGFBP-3通过与IGF紧密结合并仅在特定条件下释放IGF来调节IGF的可用性。IGFBP-3也具有IGF不依赖的作用。这种保守的多功能蛋白可能在调节衰老过程中发挥关键作用。在目标1中，我们将开发基因工具并使用它们来确定IGFBP-3在寿命调节中的作用。目的通过构建和研究表达野生型和突变型IGFBP-3的可诱导转基因株系，探讨IGFBP-3的配体结合和核定位的功能意义。拟议研究的完成将为IGFBP-3在脊椎动物长寿中的作用提供新的见解。预期的结果还将导致开发急需的方法和遗传工具，以敲除感兴趣的基因，或在这种新兴的脊椎动物模型中以组织特异性和时间受限的方式诱导基因表达。该项目开发的方法和转基因工具将广泛传播并分发给科学界。这些遗传工具和方法，结合N.Furzeri的独特特征和极短的寿命，将为研究开辟许多新的途径，并应有助于在脊椎动物衰老生物学方面的新发现。对衰老调节生物学的更好理解可能会导致诊断和治疗工具的开发，从而延长美国老龄化人口的健康寿命 各州。 与公共健康相关：该项目将测试胰岛素样生长因子结合蛋白-3的假设，即胰岛素样生长因子结合蛋白-3是一种主要的胰岛素样生长因子结合蛋白，通过使用绿松石鱼依赖和/或独立的机制来调节寿命，绿松石龙鱼是一种独特的脊椎动物，寿命只有几个月。该项目还将开发新的遗传工具，这将使在这种新的衰老生物学模型中实验性地操纵基因组成为可能。新的遗传工具，结合这种新的脊椎动物模型极短的寿命和其他独特的特征，应该有助于促进脊椎动物衰老生物学的新发现。更好地了解IGF信号在寿命调节中的作用可能会导致诊断和治疗工具的开发，从而提高美国老龄化人口的健康。