Drosophila VDAC's Role in Mitochondrial Function

果蝇 VDAC 在线粒体功能中的作用

• 批准号: 6772524
• 负责人: Brett Harrison Graham
• 金额: $ 12.88万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-07-07 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6772524
• 关键词: Drosophilidae; gene expression; genetic screening; immunocytochemistry; in situ hybridization; membrane channels; membrane proteins; mitochondria; mitochondrial membrane; mutant; northern blottings; polymerase chain reaction; protein isoforms; protein structure function; southern blotting; training; voltage /patch clamp

DESCRIPTION (provided by applicant): The applicant, a board eligible pediatrician with a Ph.D. in molecular genetics, is pursuing a fellowship in genetics. He has a long-standing and continued interest in the genetic regulation of metabolism, particularly with regards to the molecular mechanisms involved in mitochondrial function and pediatric mitochondrial disease. In pursuit of these interests, he has sought relevant clinical and research training with a long-term goal of contributing to the understanding of fundamental genetic and molecular mechanisms of mitochondrial function and biogenesis. This application provides a mechanism for achieving an immediate career goal of expanding the applicant's research experience to the fields of Drosophila genetics, development and electrophysiology necessary for the development of novel genetic models for the study of the regulation of mitochondrial function. The purpose of this study is to evaluate the specific functions of isoforms of the Voltage Dependent Anion Channel (VDAC) in Drosophila melanogaster. VDAC, the most abundant protein in the mitochondrial outer membrane, represents the main pathway across this membrane for small metabolites and ions that are essential for mitochondrial-dependent energy metabolism and has been implicated in various regulated cellular processes such as cytochrome-c dependent apoptosis and the permeability transition pore. With the recent annotation of the Drosophila genome, four genes with homology to eukaryotic VDACs have been identified, two of which demonstrate functional complementation of yeast VDAC. These four genes will be characterized in terms of transcript structure, temporal-spatial expression, and in vitro biophysical properties. An allelic series of loss of function mutations for these genes will be generated utilizing both P-element mediated mutagenesis and RNA interference. The specific functions of these Drosophila VDACs will be determined by assessing the consequences of loss of VDAC functions phenotypically on morphological, ultrastructural, cellular, biochemical, and physiological levels. Mutants that demonstrate easily scorable phenotypes will be utilized in genetic enhancer/suppressor screens designed to identify genes that interact with VDACs and are important for mitochondrial function and biogenesis. Through the identification of fundamental, conserved genetic pathways of mitochondrial regulation, this study will contribute to the understanding of mitochondrial function and highlight new genes for future study in mammalian systems as models for human mitochondrial disease and as potential therapeutic targets. The environment in which this study will be performed is uniquely suited for facilitating the applicant's career development plan. The Department of Molecular and Human Genetics at Baylor College of Medicine is renowned for its Drosophila genetics and its collaborative atmosphere. Through a combination of supervised research, scientific interchange, and selected coursework, the applicant will obtain the training necessary for a successful transition to an independent investigator.

描述（由申请人提供）：申请人是一名符合委员会资格的儿科医生，拥有博士学位。在分子遗传学领域，正在攻读遗传学奖学金。他对代谢的遗传调控有着长期持续的兴趣，特别是涉及线粒体功能和儿科线粒体疾病的分子机制。为了追求这些兴趣，他寻求相关的临床和研究培训，其长期目标是促进对线粒体功能和生物发生的基本遗传和分子机制的理解。该申请提供了一种实现直接职业目标的机制，即将申请人的研究经验扩展到果蝇遗传学、发育和电生理学领域，这对于开发用于研究线粒体功能调节的新型遗传模型是必需的。本研究的目的是评估果蝇电压依赖性阴离子通道 (VDAC) 亚型的具体功能。 VDAC 是线粒体外膜中最丰富的蛋白质，代表小代谢物和离子穿过该膜的主要途径，这些代谢物和离子对于线粒体依赖性能量代谢至关重要，并且与各种受调节的细胞过程有关，例如细胞色素 C 依赖性细胞凋亡和细胞凋亡。渗透率过渡孔。随着最近对果蝇基因组的注释，已经鉴定出四个与真核VDAC同源的基因，其中两个证明了酵母VDAC的功能互补。这四个基因将在转录结构、时空表达和体外生物物理特性方面进行表征。利用 P 元件介导的诱变和 RNA 干扰将产生这些基因的一系列等位基因功能丧失突变。这些果蝇 VDAC 的具体功能将通过评估 VDAC 功能丧失表型对形态、超微结构、细胞、生化和生理水平的影响来确定。表现出易于评分的表型的突变体将用于遗传增强子/抑制子筛选，旨在识别与 VDAC 相互作用并对线粒体功能和生物发生很重要的基因。通过鉴定线粒体调节的基本、保守的遗传途径，这项研究将有助于理解线粒体功能，并强调未来在哺乳动物系统中研究的新基因，作为人类线粒体疾病的模型和潜在的治疗靶点。进行这项研究的环境非常适合促进申请人的职业发展计划。贝勒医学院分子与人类遗传学系以其果蝇遗传学及其协作氛围而闻名。通过监督研究、科学交流和选定的课程相结合，申请人将获得成功过渡为独立研究者所需的培训。