Genetic and Epigenetic Determinants of Longevity.

长寿的遗传和表观遗传决定因素。

• 批准号: 8986459
• 负责人: Siu Sylvia Lee
• 金额: $ 43.31万
• 依托单位: CORNELL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-09-01 至 2020-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8986459
• 关键词: Age; Aging; Aging-Related Process; Alternative Splicing; Animal Model; Binding; Biological; Biological Monitoring; Biology of Aging; Caenorhabditis elegans; Cells; Chromatin; Communities; Computing Methodologies; Coupled; DNA Methylation; DNA Polymerase II; DNA Sequence; Data; Disease; Environment; Epigenetic Process; Future; Gene Expression; Gene Expression Regulation; Generations; Genes; Genetic; Genetic Models; Genetic Transcription; Genome; Genomics; Goals; Histones; Inherited; Investigation; Link; Longevity; Longevity Pathway; Lysine; Maps; Mediating; Memory; Methylation; Methyltransferase; Modeling; Modification; Molecular; Nucleosomes; Organism; Output; Pattern; Process; Proteins; RNA Interference; RNA Polymerase II; Regulation; Research; Resources; Role; Specificity; Techniques; Tertiary Protein Structure; Tissues; Untranslated RNA; age related; aging gene; base; density; epigenetic regulation; epigenome; experience; genome-wide; healthy aging; histone modification; insight; mutant; offspring; public health relevance; therapeutic development; transgenerational epigenetic inheritance

 DESCRIPTION (provided by applicant): Epigenetic regulation is a fundamental mechanism that bridges the genome with the environment, and is emerging as a key determinant of longevity. Recent findings in C. elegans have provided strong evidence that epigenetic mechanisms, in particular chromatin regulation, are intimately involved in longevity determination and its inheritance. Despite the exciting biological data, the mechanisms of how epigenetic regulation influences longevity are unclear. The long-term goal of this application is to elucidate how epigenetic regulation bridges the genome and the environment to modulate longevity. The overarching hypothesis of this proposal is that we can gain mechanistic insights into the connection of epigenetic regulation and longevity by studying longevity mutants with disrupted epigenetic mechanisms and by probing how the overall epigenetic landscape changes with age in the powerful model C. elegans. Building on recent discoveries in my lab, we will pursue three specific aims. In Aim 1, we will investigate the mechanisms by which the putative H3K9me3 methyltransferases SET-9 & SET-26 limit lifespan and maintain germline immortality. We propose to determine the longevity pathways they act in, identify the protein domains and the tissue specificity key to their action, and map their genome-wide binding profiles and transcriptional outputs. The proposed investigations will reveal how SET-9/26 influence longevity and transgenerational inheritance. In Aim 2, we will investigate the role of H3K36me3 in age-dependent gene regulation and longevity. We propose to examine whether altered RNA polymerase II-mediated transcription contributes to age-dependent gene expression changes, identify the factors that recognize the H3K36me3 mark, and monitor the biological consequence of depleting H3K36 methylation in specific cells/tissues. H3K36me3 is a ubiquitous histone modification, thus elucidating its mechanism in gene expression regulation through the aging process will provide important new insights into not only aging biology but also fundamental mechanisms of gene regulation. In Aim 3, we will investigate how the chromatin landscape changes with age. Currently not much is known about how aging impacts the general chromatin landscape in C. elegans. We propose to profile the genome-wide patterns of several key histone modifications, as well as nucleosome density, through the aging process, and use computational methods to uncover age-dependent patterns that can generate testable hypotheses for future studies. Findings from our proposed investigations will provide a much-needed framework for integrating emerging functional data to understand how the epigenome modulates aging and longevity in C. elegans. The data generated in this aim will also be a useful resource for the aging and gene regulation research community. The proposed research will provide substantial new insights into how epigenetic mechanisms influence aging and longevity in the key model organism C. elegans, and will more broadly impact the understanding of the epigenetic basis of longevity in diverse organisms.

 描述（由申请人提供）：表观遗传调控是连接基因组与环境的基本机制，并且正在成为长寿的关键决定因素。最近的研究结果在C.秀丽线虫提供了强有力的证据，即表观遗传机制，特别是染色质调节，与寿命决定及其遗传密切相关。尽管有令人兴奋的生物学数据，表观遗传调控如何影响寿命的机制尚不清楚。这项应用的长期目标是阐明表观遗传调控如何连接基因组和环境以调节寿命。这个建议的首要假设是，我们可以通过研究具有破坏的表观遗传机制的长寿突变体，并通过探索强大的模型C中整体表观遗传景观如何随年龄变化，来获得对表观遗传调节与长寿之间联系的机械见解。优雅的基于我实验室最近的发现，我们将追求三个具体目标。在目标1中，我们将研究推定的H3 K9 me 3甲基转移酶SET-9和SET-26限制寿命和维持种系永生的机制。我们建议确定长寿途径，他们的行为，确定蛋白质结构域和组织特异性的关键，他们的行动，并映射其全基因组的结合概况和转录输出。拟议的调查将揭示SET-9/26如何影响寿命和跨代遗传。在目标2中，我们将研究H3 K36 me 3在年龄依赖性基因调控和长寿中的作用。我们建议检查是否改变RNA聚合酶II介导的转录有助于年龄依赖性基因表达的变化，确定识别H3 K36 me 3标记的因素，并监测特定细胞/组织中耗尽H3 K36甲基化的生物学后果。H3 K36 me 3是一种普遍存在的组蛋白修饰，因此阐明其在衰老过程中的基因表达调控机制将为衰老生物学和基因调控的基本机制提供重要的新见解。在目标3中，我们将研究染色质景观如何随年龄变化。目前，人们对衰老如何影响C的一般染色质景观知之甚少。优雅的我们建议通过衰老过程来分析几个关键组蛋白修饰的全基因组模式以及核小体密度，并使用计算方法来揭示年龄依赖性模式，这些模式可以为未来的研究产生可检验的假设。我们提出的研究结果将提供一个急需的框架，整合新兴的功能数据，以了解表观基因组如何调节C。优雅的这一目标产生的数据也将成为衰老和基因调控研究界的有用资源。这项拟议中的研究将为表观遗传机制如何影响关键模式生物C的衰老和寿命提供实质性的新见解。elegans，并将更广泛地影响对不同生物体中长寿的表观遗传基础的理解。