Development of Germplasm Resources for Preservation of Aquatic Models

水生模型保存种质资源开发

基本信息

批准号：
8270027
负责人：
Terrence Robert Tiersch
金额：
$ 8.75万
依托单位：
LOUISIANA STATE UNIV AGRICULTURAL CENTER
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-09-01 至 2012-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8270027
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 Databases 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 cost effective 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

项目摘要

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）：迫切需要改善斑马鱼和青鳉等水生模式生物遗传资源的保存。通过冷冻保存研究线的可用性将深刻影响毒理学、胚胎学、遗传学、药物开发和人类疾病等生物医学研究的进步。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型、转基因型和野生型鱼品系。然而，这些生产线的实时维护成本高昂、风险较大，甚至超出了最大的库存中心当前的能力。尽管冷冻保存是长期保存遗传物质的一种行之有效的方法，但目前的鱼类方案尚未标准化，产生的结果不一致，并威胁到大规模遗传筛查的有效性。为了使精子冷冻保存成为鱼类遗传库的可靠、经济有效的工具，需要改进整个冷冻保存过程并将其集成到一个高效的大型平台中，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。我们的项目目标是通过优化、简化和标准化程序以及应用基本的冷冻生物学和生理参数，建立斑马鱼和青鳉精子的高通量冷冻保存，供库存中心应用和研究实验室使用。我们将评估以下因素的影响：1) 动物调节，2) 样品采集，3) 精子浓度，4) 补充剂成分，5) 添加剂，6) 冷藏储存和运输，7) 冷冻保护剂毒性，8) 冷却速率和温度的相互作用冷冻保护剂，9) 解冻，10) 解冻后修正，以及 11) 受精程序。我们将建立以下方面的高通量样品管理：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加工。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并标准化程序。种质冷冻保存将通过以下方式极大地加强 NIH 资源的开发、管理和分配：1) 减少设施规模和生产成本，2) 保护遗传多样性并减少近亲繁殖，3) 最大限度提高活体动物饲养效率，3) 促进全球、遗传物质的区域和机构运输。