Molecular mechanisms linking epigenetic changes to longevity
Molecular mechanisms linking epigenetic changes to longevity
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
关键词:
AddressAgeAgingAnimalsAwardBindingCREB1 geneCaenorhabditisCaenorhabditis elegansCapsid ProteinsCell AgingCell physiologyCellsChIP-seqChromatinCollaborationsComplementComplexDataDiseaseDown-RegulationEndoplasmic ReticulumEnsureEnzymesEpigenetic ProcessFRAP1 geneFatty acid glycerol estersFoundationsGene ExpressionGene Expression ProfilingGeneticGenetic TranscriptionGenomic approachGoalsGolgi ApparatusHMGB1 ProteinHistone H3HomeostasisIncidenceLeadLinkLipidsLongevityLysineMalignant NeoplasmsMammalian CellMammalsMediatingMentorsMetabolicMetabolic DiseasesMetabolismMethyltransferaseMicroscopyModelingModificationMolecularMonounsaturated Fatty AcidsNerve DegenerationPathway interactionsPhasePhysiologicalPost-Translational Protein ProcessingProcessProteinsProteomicsPublic HealthPublishingRNA SplicingRegulationResearchResearch PersonnelRoleSignal TransductionSystemTestingTissuesTrainingTranscription CoactivatorTranscriptional RegulationTranslatingUniversitiesVesicleVocational GuidanceWorkage relatedbasecareerchromatin modificationepigenetic regulationexperimental studyhistone modificationinnovationlipid metabolismmetabolomicsnext generationnovelprogramsprotein complexresponsespatiotemporalsuccesstooltraffickingtranscription factortransgenerational epigenetic inheritance
中文摘要
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.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
-
批准号:JCZRQN202500010
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
-
批准号:2025JJ70209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
-
批准号:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
-
批准号:2023JJ50274
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
-
批准号:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
-
批准号:81973577
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
-
批准号:81602908
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: