Maintenance of Mitochondrial Protein Folding as an Aging Effector

维持线粒体蛋白折叠作为衰老效应器

• 批准号: 8235175
• 负责人: Cole M Haynes
• 金额: $ 37.12万
• 依托单位: SLOAN-KETTERING INST CAN RESEARCH
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-15 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8235175
• 关键词: 5' Untranslated Regions; Address; Age; Age of Onset; Aging; Aging-Related Process; Animals; Attenuated; Binding; Biogenesis; Caenorhabditis elegans; Caloric Restriction; Cell Nucleus; Cells; Chaperone Gene; Complex; DNA biosynthesis; Development; Disease; Electron Transport; Environment; Event; Friedreich Ataxia; Genetic Transcription; Homeostasis; Inner mitochondrial membrane; Life; Longevity; Maintenance; Malignant Neoplasms; Mediating; Metabolic; Mitochondria; Mitochondrial Matrix; Mitochondrial Proteins; Molecular; Molecular Chaperones; Mutation; Nutrient; Organelles; Output; Parkinson Disease; Pathway interactions; Peptide Hydrolases; Peptide Initiation Factors; Peptides; Phosphorylation; Phosphotransferases; Physiological; Proteins; Pump; Quality Control; Reactive Oxygen Species; Regulation; Resistance; Role; Signal Pathway; Signal Transduction; Stress; Stress Response Signaling; Time; Transcript; Translating; Translations; attenuation; biological adaptation to stress; deprivation; gain of function; mitochondrial dysfunction; mitochondrial genome; mutant; protein folding; protein function; research study; response; therapeutic development; trafficking; transcription factor

DESCRIPTION (provided by applicant): Mitochondrial function and protein homeostasis are key contributors to the aging process and the onset of age- associated diseases. This proposal describes plans to examine mitochondrial protein folding and function in the context of C. elegans development and aging to further elucidate the molecular mechanisms cells employ to protect organelle function. Mitochondria are dynamic organelles, which are remodeled during diverse conditions including nutrient deprivation and cellular differentiation. Mitochondrial metabolic output has long been appreciated as a contributor to the aging process, primarily through the detrimental effects of reactive oxygen species generated by the electron transport chain. Additionally, mutations in the mitochondrial genome accumulate over time due to errors introduced during DNA replication. Both forms of damage challenge the already complex protein-folding environment in the organelle. To function properly during organelle remodeling and stress, the mitochondrial protein-folding environment must be maintained by molecular chaperones and proteases. We have identified a mitochondrial unfolded protein response, a signaling pathway that adjusts the organelle's folding capacity to the load of unfolded proteins that accumulate during stress by regulating the expression of mitochondrial chaperone genes. And, more recently we have discovered a requirement for a complementary translation regulation pathway. Consistent with a role in organelle protection, animals lacking components of either pathway are sensitive to conditions that perturb mitochondrial function. Here, we describe plans to further elucidate the mechanism of signal transduction within each pathway as well as their impact on development, aging and age-associated damage. Additionally, we plan to uncouple activation of each stress response pathway from mitochondrial biogenesis or stress to expand organelle folding capacity and determine the impact on lifespan and resistance to proteotoxicity. PUBLIC HEALTH RELEVANCE: Mitochondrial dysfunction is prevalent in diseases ranging from Parkinson's and Friedreich's ataxia to cancer. Cells respond to mitochondrial insults but the stress responses are eventually overwhelmed leading to the disease state. A thorough understanding of the molecular pathways cells employ to protect against mitochondrial dysfunction will allow for the development of therapeutic manipulations potentially able to limit age or disease-associated mitochondrial damage.

描述（由申请人提供）：线粒体功能和蛋白质稳态是衰老过程和年龄相关疾病发作的关键因素。该提案描述了在C. elegans的发育和衰老，以进一步阐明细胞保护细胞器功能的分子机制。线粒体是一种动态的细胞器，在不同的条件下，包括营养剥夺和细胞分化过程中会发生重塑。线粒体代谢输出长期以来一直被认为是衰老过程的贡献者，主要是通过电子传递链产生的活性氧的有害影响。此外，由于DNA复制过程中引入的错误，线粒体基因组中的突变随着时间的推移而积累。这两种形式的损伤都挑战了细胞器中已经复杂的蛋白质折叠环境。为了在细胞器重塑和应激期间正常发挥作用，线粒体蛋白折叠环境必须由分子伴侣和蛋白酶维持。我们已经确定了一个线粒体未折叠蛋白质的反应，一个信号通路，调节细胞器的折叠能力，以负荷未折叠蛋白质，积累在压力通过调节线粒体伴侣基因的表达。而且，最近我们发现了一个互补的翻译调节途径的要求。与细胞器保护的作用一致，缺乏任一途径的组分的动物对扰乱线粒体功能的条件敏感。在这里，我们描述了计划，以进一步阐明每个通路内的信号转导机制，以及它们对发育，衰老和年龄相关损伤的影响。此外，我们计划将每个应激反应途径的激活与线粒体生物发生或应激解偶联，以扩大细胞器折叠能力，并确定对寿命和蛋白毒性抗性的影响。 公共卫生相关性：线粒体功能障碍在从帕金森氏症和弗里德赖希共济失调到癌症的疾病中普遍存在。细胞对线粒体损伤作出反应，但应激反应最终被压倒，导致疾病状态。对细胞用于防止线粒体功能障碍的分子途径的透彻理解将允许开发可能能够限制年龄或疾病相关的线粒体损伤的治疗操作。