Development of Germplasm Resources for Preservation of Aquatic Models

水生模型保存种质资源开发

• 批准号: 7813859
• 负责人: Terrence Robert Tiersch
• 金额: $ 53.36万
• 依托单位: LOUISIANA STATE UNIV AGRICULTURAL CENTER
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-01 至 2012-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7813859
• 关键词: Address; Adoption; Agreement; Amendment; Animal Model; Animals; Applied Research; Biological; Biological Preservation; Biological databases; Biomedical Research; Bovine Serum Albumin; Chemicals; Cloning; Collaborations; Communities; Complement; Cryopreservation; Databases; Development; Diet; Educational workshop; Embryology; Enhancers; Equipment; Equipment and supply inventories; Evaluation; Fertilization; Fishes; Freezing; Future; Gene Transfer; Genes; Genetic; Genetic Materials; Genetic Screening; Genetic Variation; Germ Cells; Goals; Human Resources; Inbreeding; Information Networks; Internet; Japanese Killifish; Label; Laboratories; Laboratory Research; Life; Link; Maintenance; Measures; Methods; Modeling; Pathway interactions; Physiological; Plastics; Population; Procedures; Process; Production; Protocols documentation; Quality Control; Research; Research Personnel; Resources; Role; Sampling; Security; Shipping; Ships; Standardization; Testis; Toxic effect; Toxicology; Training; Transgenic Organisms; United States National Institutes of Health; Work; Zebrafish; aquatic organism; base; biosecurity; cell motility; conditioning; cost; design; drug development; genetic resource; high standard; human disease; improved; male; meetings; member; mutant; operation; prevent; programs; quality assurance; reproductive; sample collection; seal; sperm cell; tool

DESCRIPTION (provided by applicant): There is an immediate need to improve preservation of genetic resources from aquatic model organisms such as zebrafish and medaka. The availability of research lines through cryopreservation will profoundly influence the advancement of biomedical research in toxicology, embryology, genetics, drug development, and human disease. In the past 15 years, laboratories around the world have produced thousands of mutant, transgenic and wild-type fish lines. However, live maintenance of these lines is expensive, risky, and beyond the current capacity of even the largest stock centers. Although cryopreservation is a proven method for long-term maintenance of genetic material, current protocols for fish are not standardized, yield inconsistent results, and threaten the efficacy of large-scale genetic screening. For sperm cryopreservation to become a reliable, cost-effective tool for genetic banking of fish, the overall cryopreservation process needs to be improved and integrated into an efficient large-scale platform that links with genetic and biological databases, archival storage capabilities, inventory management, and sample distribution pathways. Our Project Goal is to establish high-throughput cryopreservation of zebrafish and medaka sperm for stock center application and for research laboratory use by optimizing, streamlining, and standardizing procedures, and by applying basic cryobiological and physiological parameters. We will evaluate the effects of: 1) animal conditioning, 2) sample collection, 3) sperm concentration, 4) extender composition, 5) additives, 6) refrigerated storage and transport, 7) cryoprotectant toxicity, 8) interactions of cooling rate and cryoprotectants, 9) thawing, 10) post-thaw amendments, and 11) fertilization procedures. We will establish high-throughput sample management of: 1) straw-filling and sealing, 2) labeling, 3) inventory management, 4) shipping reliability, and 5) adoption of automated processing of high-security plastic straws. We will define terms and standardize procedures for quality control and biosecurity at stock centers and donor laboratories. Germplasm cryopreservation will greatly enhance development, management, and distribution of NIH resources by: 1) reducing size and production costs of facilities, 2) protecting genetic diversity and reducing inbreeding, 3) maximizing efficiency of holding live animals, and 3) facilitating global, regional, and institutional transport of genetic material.

描述（由申请人提供）：目前迫切需要改善对斑马鱼和青鳉等水生模式生物遗传资源的保护。通过冷冻保存获得的研究细胞系将深刻影响毒理学、胚胎学、遗传学、药物开发和人类疾病等生物医学研究的进展。在过去的15年里，世界各地的实验室已经生产了数千种突变、转基因和野生型的鱼类。然而，这些生产线的现场维护是昂贵的，有风险的，甚至超过了最大的库存中心的当前能力。虽然冷冻保存是一种经过验证的长期保存遗传物质的方法，但目前的鱼类方案并不标准化，产生不一致的结果，并威胁到大规模遗传筛选的有效性。为了使精子冷冻保存成为一种可靠的、具有成本效益的鱼类基因库工具，需要改进整个冷冻保存过程，并将其整合到一个高效的大规模平台中，该平台与遗传和生物数据库、档案存储能力、库存管理和样本分配途径相联系。我们的项目目标是通过优化、简化和标准化程序，并通过应用基本的低温生物学和生理学参数，建立斑马鱼和青鳉精子的高通量冷冻保存技术，供储备中心应用和研究实验室使用。我们将评价以下因素的影响：1）动物调节、2）样本采集、3）精子浓度、4）稀释液成分、5）添加剂、6）冷藏储存和运输、7）冷冻保护剂毒性、8）冷却速率和冷冻保护剂的相互作用、9）解冻、10）解冻后改良和11）受精程序。我们将建立高通量的样品管理：1）吸管填充和密封，2）标签，3）库存管理，4）运输可靠性，以及5）采用高安全性塑料吸管的自动化处理。我们将为库存中心和捐赠实验室的质量控制和生物安全定义术语和标准化程序。种质冷冻保存将通过以下方式极大地促进NIH资源的开发、管理和分配：1）减少设施的规模和生产成本; 2）保护遗传多样性和减少近亲繁殖; 3）最大限度地提高保存活体动物的效率; 3）促进遗传物质的全球、区域和机构运输。