CONSORTIUM FOR LARGE-SCALE PRODUCTION AND CRYOPRESERVATION OF KNOCKOUT MICE

基因敲除小鼠大规模生产和冷冻保存联盟

• 批准号: 8356914
• 负责人: MONICA J. JUSTICE
• 金额: $ 412.68万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-01 至 2012-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8356914
• 关键词: Adult; Alleles; Behavior; Biological; Biological Assay; Breeding; Cell physiology; Code; Cryopreservation; Cystic Fibrosis; Data; Data Coordinating Center; Deposition; Development; Disease; Embryo; Embryonic Development; Fertility; Functional RNA; Funding; Gene Targeting; Genes; Genome; Glean; Grant; Health; Human; Human Genome; Institutes; Knockout Mice; Knowledge; LacZ Genes; Malignant Neoplasms; Medicine; Metabolic; Mus; Mutant Strains Mice; National Center for Research Resources; Organism; Pattern; Persons; Physiological; Physiology; Principal Investigator; Proteins; Research; Research Infrastructure; Resources; Route; Source; Stress; System; Technology; Tissues; United States National Institutes of Health; Variant; Work; body system; college; cost; embryonic stem cell; gene function; large scale production; loss of function; mutant; programs; repository

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. DESCRIPTION (provided by applicant): Annotation of the reference human genome has identified approximately 20,000 protein coding genes as well as 3,000 non-coding RNAs. Together these genes orchestrate the development of the organism, supporting all aspects of the function of cells, tissues, organ systems as well physiology and behavior. The l000 genomes project has revealed extraordinary levels of diversity in human genomes, yet for most genes neither the function of normal version nor the disease consequence of loss-of-function variants is known. The mouse provides a route to understand the function of genes and their variants. Mice share developmental, physiological, anatomical and metabolic parallels with humans, which are evident in healthy as well as diseased states. These reflect similarities of the genes in both species. Mutant mice generated using ES cell technology are a sensitive biological assay system from which a deep understanding of function can be gleaned and they also provide a long lasting biological resource for further study. The objective of this proposal is to generate mutant mice from a resource of ES cells with conditionally targeted, lacZ-tagged alleles generated under previous NIH (KOMP) and EU (EUCOMM) funded programs. We and others will use these mice to discover the function of genes. We are proposing to carry out this work at scale and have formed a consortium of three Institutes (Baylor College of Medicine, the Sanger Institute and MRC Harwell) to work together as equal partners to achieve this objective. We will generate mice corresponding to 1500 mutant genes from ES cells distributed by the Sanger Institute. We will characterize the adult and embryonic expression pattern of the each targeted gene and by breeding determine the requirement of each for embryonic development and fertility, if any. All of the alleles will be cryo-preserved and placed in a repository and all of the data will be deposited in a centralized data coordination center to support further studies. RELEVANCE: Most of the 20,000 genes in a typical person are normal but we also have several hundred broken ones. While some broken genes can cause severe disease such as cystic fibrosis or cancer, others have little or no consequence, or function only under stress. Currently we have some understanding of the function of just one third of human genes. If we are to fully understand human health and disease we must expand knowledge of gene function to all of our genes.

该子项目是利用资源的众多研究子项目之一 由 NIH/NCRR 资助的中心拨款提供。子项目的主要支持 并且子项目的主要研究者可能是由其他来源提供的， 包括其他 NIH 来源。 子项目可能列出的总成本 代表子项目使用的中心基础设施的估计数量， NCRR 赠款不直接向子项目或子项目工作人员提供资金。 描述（由申请人提供）：参考人类基因组的注释已鉴定出大约 20,000 个蛋白质编码基因以及 3,000 个非编码 RNA。这些基因共同协调有机体的发育，支持细胞、组织、器官系统以及生理和行为的各个方面的功能。千个基因组计划揭示了人类基因组中非凡的多样性水平，但对于大多数基因来说，正常版本的功能和功能丧失变异的疾病后果都是未知的。小鼠提供了了解基因及其变体功能的途径。小鼠在发育、生理、解剖和代谢方面与人类相似，这在健康和患病状态下都很明显。这些反映了两个物种基因的相似性。使用ES细胞技术产生的突变小鼠是一种灵敏的生物检测系统，可以从中深入了解其功能，并为进一步研究提供持久的生物资源。该提案的目的是从 ES 细胞资源中产生突变小鼠，这些细胞具有在先前 NIH (KOMP) 和 EU (EUCOMM) 资助的项目下产生的有条件靶向、lacZ 标记等位基因。我们和其他人将利用这些小鼠来发现基因的功能。我们提议大规模开展这项工作，并组建了由三个研究所（贝勒医学院、桑格研究所和 MRC Harwell）组成的联盟，作为平等的合作伙伴共同努力实现这一目标。我们将从桑格研究所分发的 ES 细胞中培育出与 1500 个突变基因相对应的小鼠。我们将表征每个目标基因的成体和胚胎表达模式，并通过育种确定每个目标基因对胚胎发育和生育力的要求（如果有）。所有等位基因将被冷冻保存并放置在存储库中，所有数据将存放在中央数据协调中心以支持进一步的研究。 相关性：一般人的 20,000 个基因中大部分都是正常的，但也有数百个损坏的基因。虽然一些断裂的基因可能导致严重的疾病，如囊性纤维化或癌症，但其他基因则几乎没有后果，或者仅在压力下发挥作用。目前我们对人类基因的功能只有三分之一有了一定的了解。如果我们要充分了解人类健康和疾病，我们必须将基因功能的知识扩展到我们所有的基因。