课题基金 / 基金详情

CENTER TO CHARACTERIZE & MAINTAIN MUTANT MICE

CENTER TO CHARACTERIZE & MAINTAIN MUTANT MICE
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批准号:
6053577
负责人:
TERRY A VAN DYKE
金额:
$85.75万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-09-30 至 2004-08-31

项目摘要

项目成果

TERRY A VAN DYKE的其他基金

相关文献

中文摘要
翻译
在过去的20年里,生物医学研究经历了促进小鼠基因组操作技术的爆炸式发展。这些技术对大多数研究人员来说都很容易获得,因此,大量有价值的诱导突变小鼠品系正在不断产生。鉴于单个实验室维护和分发这些菌株的高成本,我们必须开发高效的专家资源中心来进口,表征和分发突变小鼠。这些设施应该在菌株的维护和繁殖方面保持高标准,促进我们对最广泛使用的菌株的理解,并开发促进这些菌株高效产生和表型分析的技术。北卡罗来纳大学长期致力于在生物医学研究中使用老鼠,大量杰出的北卡罗来纳大学研究人员致力于这种方法就是证据。UNC为大量无病原体小鼠提供最先进的住房和支持设施,以及能够进行小鼠模型研究的核心研究设施。这些包括动物模型、组织病理学、临床化学和RIA核心。在所有级别配备这些资源的特殊人员。UNC-MMRRC的具体目标是:(1)导入、重新衍生、基因分型、维持和分发新的小鼠品系。第一年将进口15个新菌株,随后每年增加到30个新菌株;(2)超低温保存新的和现有的突变菌株;(3)与IMR和其他MMRRC节点进行数据采集、存储、交换和技术开发的接口;(4)在组织病理、生理、细胞生物学和分子异常方面,对一定数量的小鼠品系进行表型表征。北卡罗来纳大学在癌症、心血管生物学、免疫学和神经科学等领域具有广泛的分析能力;(5)培养从体细胞中高效“克隆”小鼠的能力。在北卡罗来纳大学动物模型中心,长尾鲨博士将扩大奥利弗·史密斯博士实验室目前的努力;(6)开发“报告”小鼠品系,以促进特定细胞/组织类型的快速表型。作为开发/提供这种菌株单独或诱导突变背景的可行性的测试系统,将获得或产生和研究在特定细胞类型中表达绿色荧光蛋白(GFP)的有限数量的菌株。
英文摘要
In the past 20 years biomedical research has experienced an explosion in the technologies that facilitate manipulation of the mouse genome. These technologies are readily accessible to most investigators, and as a result, a tremendous number of valuable induced mutant mouse strains are being continuously generated. Given the high cost to individual laboratories for the maintenance and distribution of such strains, it is essential that we develop high efficiency expert resource centers to import, characterize and distribute mutant mice. Such facilities should maintain high standards in the maintenance and propagation of strains, advance our understanding of the most broadly useful strains, and develop technologies that facilitate the efficient generation and phenotypic analysis of such strains. UNC has had a long standing commitment to the use of the mouse in biomedical research, as evidenced by the large number of prominent UNC investigators committed to this approach. UNC maintains state of the art housing and support facilities for large numbers of pathogen-free mice, along with core research facilities that enable mouse model studies. These include the Animal Models, Histopathology, Clinical Chemistry, and RIA cores. Exceptional personnel staff these resources at all levels. Specific aims of the UNC-MMRRC are to: (1) Import, rederive, genotype, maintain and distribute new mouse strains. In the first year, 15 new strains will be imported, growing to 30 new strains per year in subsequent years; (2) Cryopreserve new and existing mutant strains; (3) Interface with the IMR and other MMRRC nodes in the acquisition, storage, and exchange of data and the development of technologies; (4) Phenotypically characterize a specified number of mouse strains with regard to histopathological, physiological, cell biological and molecular abnormalities. Special expertise at UNC for possible extensive analyses exists in the fields of Cancer, Cardiovascular Biology, Immunology, and Neuroscience; (5) Develop the ability to efficiently "clone" mice from somatic cells. In the UNC Animal Models Core, Dr. Thresher will expand current efforts by the Dr. Oliver Smithies' lab; (6) Develop "reporter" mouse strains that will facilitate rapid phenotyping within particular cell/tissue types. As a test system for the feasibility of developing/providing such strains alone or induced mutant backgrounds, a limited number of strains that express green fluorescent protein (GFP) in specific cell types will be obtained or generated and studied.
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PRECLINICAL MOUSE MODELS: CENTRAL NERVOUS SYSTEM CANCERS
PRECLINICAL MOUSE MODELS: CENTRAL NERVOUS SYSTEM CANCERS
PRECLINICAL MOUSE MODELS: CENTRAL NERVOUS SYSTEM CANCERS
Animal Models Core