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Molecular mechanisms linking epigenetic changes to longevity

Molecular mechanisms linking epigenetic changes to longevity
将表观遗传变化与长寿联系起来的分子机制
批准号:
10226359
负责人:
Carlos Giovanni Silva-García
金额:
$12.89万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-08-01 至 2023-01-31

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中文摘要
翻译
项目摘要 面对不断增长的人口老龄化,了解控制衰老过程的分子机制至关重要 与年龄有关的疾病的发病率。随着年龄的增长,表观遗传调控的丧失已经成为衰老的一个标志, 但人们对染色质改变与长寿之间的联系机制知之甚少。最近,与 在斯坦福大学的Brunet实验室,我们展示了秀丽线虫染色质的变化 生殖系,特别是组蛋白H3(H3K4me3)上赖氨酸4的三甲基化缺陷 与Set1(COMPASS)相关,诱导mTOR靶基因表达的变化 通过特定富集单不饱和脂肪酸延长寿命的躯体组织的代谢变化 (多不饱和脂肪酸)。这种作用是由SREBP1/SBP-1转录因子介导的,该转录因子通过COPII- 介导的内质网到高尔基体的转运。最近在哺乳动物中的数据强调了CREB调控的关键作用 转录共激活因子(CRTC)2在COPII交易中,而我们已经证明唯一的线虫CRTC 调节衰老和能量代谢。令人兴奋的是,我的初步数据表明CRTC-1特别是 调节H3K4me3缺陷动物的寿命延长,确立CRTC-1在表观遗传学中的新作用 对老龄化的调控。我的长期目标是理解表观遗传调控如何将环境和 影响基因表达和下游细胞过程的内部信号,以促进寿命和 跨代利益。这项提议将结合遗传学、显微镜、代谢组学和 基因组学方法揭示介导H3K4me3依赖的长寿的分子机制。目标1 将定义指南针染色质复合体的时空要求,以调节寿命和它的 效应器,如CRTC-1、SREBP1/SBP-1和mTOR靶标。为了补充这些研究,目标2将确定 CRTC-1特定功能调节的下游分子机制和代谢变化 促进H3K4me3依赖的长寿。独立的R00阶段将专注于研究跨代 COMPASS-mTOR-CRTC途径下游的机制促进长寿。自然资源的保护 所有这些组件将使我能够在这里将这些发现转化为哺乳动物系统,以识别细胞 以及表观遗传修饰控制的促进长寿的生理反应。总而言之,这些发现 将作为我的研究计划的基础,并将启动我独立研究的开始 职业生涯。我的主要导师威廉·梅尔博士将提供重要的科学和职业指导,以确保我的 成功。我的顾问和合作者补充了Mair博士的专业知识,并将帮助我实现我的职业生涯 研究目标。K99/R00奖是我在学术道路上前进的独特机会。它 将帮助我巩固在衰老表观遗传学研究中的创新利基,并为我提供 必要的学术和技术培训,以开启我作为独立调查员的职业生涯。
英文摘要
Project Summary Understanding molecular mechanisms that govern the aging process is critical in the face of the ever-increasing incidence of age-related diseases. Loss of epigenetic regulation with age has emerged as a hallmark of aging, but little is known about the mechanisms linking chromatin alterations to longevity. Recently, in collaboration with the Brunet lab at Stanford University, we demonstrated that chromatin changes in the Caenorhabditis elegans germline, specifically a deficiency in trimethylation of lysine 4 on histone H3 (H3K4me3) via the Complex Proteins Associated with Set1 (COMPASS), induce changes in expression of mTOR targets which orchestrate a metabolic shift in somatic tissues to extend lifespan via a specific enrichment of mono-unsaturated fatty acids (MUFAs). This effect is mediated by the SREBP1/SBP-1 transcription factor, which is activated through COPII- mediated ER-to-Golgi transport. Recent data in mammals highlighted a critical role for CREB regulated transcriptional coactivator (CRTC)2 in COPII trafficking, while we have shown that the sole C. elegans CRTC modulates aging and energetic metabolism. Excitingly, my preliminary data indicate that CRTC-1 specifically regulates lifespan extension in H3K4me3-deficient animals, establishing a novel role of CRTC-1 in the epigenetic regulation of aging. My long-term goal is to understand how epigenetic regulation integrates environmental and internal signals to influence gene expression and downstream cellular processes to promote longevity and transgenerational benefits. This proposal will use a combination of genetics, microscopy, metabolomics, and genomic approaches to uncover the molecular mechanisms that mediate H3K4me3-dependent longevity. Aim 1 will define the spatiotemporal requirements of the COMPASS chromatin complex to mediate longevity and its effectors such as CRTC-1, SREBP1/SBP-1 and mTOR targets. To complement these studies, Aim 2 will identify the downstream molecular mechanisms and metabolic changes that a specific function of CRTC-1 regulates to promote H3K4me3-dependent longevity. The independent R00 phase will focus on studying transgenerational mechanisms downstream of the COMPASS-mTOR-CRTC pathway to promote longevity. The conservation of all these components will allow me here to translate these findings into mammalian systems to identify the cellular and physiological responses that epigenetic modifications control to promote longevity. Together, these findings will serve as the foundation of my research program and will launch the beginning of my independent research career. My primary mentor, Dr. William Mair will provide important scientific and career guidance to ensure my success. My advisors and collaborators complement Dr. Mair’s expertise and will help me reach my career and research goals. The K99/R00 award constitutes a unique opportunity for my advance in the academic track. It will help me to consolidate an innovative niche in the study of epigenetics of aging and provide me with the necessary academic and technical training to launch my career as an independent investigator.
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Molecular Mechanisms Linking Epigenetic Changes to Longevity
  • 批准号:
    10600392
  • 项目类别:
  • 资助金额:
    $12.91万
  • 财政年份:
    2020
  • 负责人:
    Carlos Giovanni Silva-García
  • 依托单位:
Molecular mechanisms linking epigenetic changes to longevity
  • 批准号:
    10756324
  • 项目类别:
  • 资助金额:
    $24.9万
  • 财政年份:
    2020
  • 负责人:
    Carlos Giovanni Silva-García
  • 依托单位:
Molecular mechanisms linking epigenetic changes to longevity
  • 批准号:
    10055463
  • 项目类别:
  • 资助金额:
    $12.89万
  • 财政年份:
    2020
  • 负责人:
    Carlos Giovanni Silva-García
  • 依托单位:
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