Genetic Screens for Mitochondrial Phenotypes in ES Cells

ES 细胞线粒体表型的遗传筛选

• 批准号: 7173800
• 负责人: Brett Harrison Graham
• 金额: $ 7.11万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-02-17 至 2007-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7173800
• 关键词: A Mouse; Arts; Biochemical; Biological Models; Biological Process; Biology; Candidate Disease Gene; Cells; Clinical; Complementary DNA; Development; Disease; Dyes; ES Cell Line; Embryo; Environment; Fluorescence-Activated Cell Sorting; Genes; Genetic; Genetic Predisposition to Disease; Genetic Screening; Goals; Individual; Mammalian Genetics; Mango - dietary; Medicine; Membrane Potentials; Minority; Mitochondria; Mitochondrial Diseases; Mitochondrial Myopathies; Molecular; Morphology; Mus; Muscle; Mutagenesis; Myopathy; Pathogenesis; Pathway interactions; Phenotype; Prevalence; Proteins; Race; Reagent; Research; Skeletal system; Specificity; System; Whole Organism; college; cyanine; design; embryonic stem cell; high throughput analysis; insight; mitochondrial membrane; mutant; novel; novel strategies; novel therapeutics; programs; promoter; retroviral-mediated; stem; therapeutic target; tool

DESCRIPTION (provided by applicant): Mitochondrial myopathy is an important cause of skeletal muscle disease and is a common clinical feature of many mitochondrial disorders. Recent epidemiological evidence suggests that the prevalence of mitochondrial diseases may be as high as 1 in 8500. Despite important insights into the clinical, biochemical, and molecular characterization of these disorders, specific genetic etiologies have been identified in only a minority of cases, and the underlying molecular pathogenesis remains poorly understood. The overall goal of this project is to provide new insights into mitochondrial biology by performing genetic screens in mouse embryonic stem (ES) cells designed to identify genes that are important for mitochondrial function and that are possible etiological candidates for mitochondrial myopathies. ES cells mutagenized by a promoter-trap strategy that demonstrate an abnormal mitochondrial phenotype will be selected by fluorescence-activated cell sorting (FACS) using fluorescent markers for mitochondrial mass and mitochondrial membrane potential. Clones with reproducible altered mitochondrial mass and/or mitochondrial membrane potential as indicated by FACS will then be analyzed by 5' RACE to identify the altered gene. Mutant clones will then be further characterized on biochemical, morphological, and ultrastructural levels. Genetic specificity will be demonstrated by phenotypic rescue of mutant clones transfected by the cDNA of the candidate gene. By combining the genetic tractability of mouse ES cells with the high-throughput phenotyping capacity of FACS, this proposal offers a novel, rapid approach for identifying genes important for mitochondrial function in a mammalian system well-suited for studying muscle biology. The environment in which this study will be performed is uniquely suited for supporting the applicant's development of a research program in mitochondrial myopathy and biology. Baylor College of Medicine is renowned for its mammalian genetics and provides access to a state of the art FACS core.

描述（由申请人提供）：线粒体肌病是骨骼肌疾病的重要病因，是许多线粒体疾病的共同临床特征。最近的流行病学证据表明，线粒体疾病的患病率可能高达1 / 8500。尽管对这些疾病的临床、生化和分子特征有重要的认识，但仅在少数病例中确定了特定的遗传病因，并且潜在的分子发病机制仍然知之甚少。该项目的总体目标是通过在小鼠胚胎干（ES）细胞中进行基因筛选，旨在鉴定对线粒体功能重要的基因和线粒体肌病可能的病因候选基因，从而为线粒体生物学提供新的见解。通过启动子诱捕策略诱变的线粒体表型异常的ES细胞将通过荧光激活细胞分选（FACS）选择线粒体质量和线粒体膜电位的荧光标记。通过FACS检测，具有可复制的线粒体质量和/或线粒体膜电位改变的克隆将通过5' RACE进行分析，以识别改变的基因。突变克隆将进一步在生化、形态和超微结构水平上进行表征。基因特异性将通过转染候选基因cDNA的突变克隆的表型拯救来证明。通过将小鼠胚胎干细胞的遗传易感性与FACS的高通量表型能力相结合，该建议提供了一种新的，快速的方法来鉴定哺乳动物系统中对线粒体功能重要的基因，非常适合研究肌肉生物学。该研究的环境非常适合支持申请人在线粒体肌病和生物学方面的研究项目的发展。贝勒医学院以其哺乳动物遗传学而闻名，并提供最先进的FACS核心。