The Role of Enhancer of Zeste Homolog 2 in Cellular Senescence

Zeste 同源物 2 增强子在细胞衰老中的作用

• 批准号: 8847615
• 负责人: Takahiro Ito
• 金额: $ 4.31万
• 依托单位: BROWN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-07-01 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8847615
• 关键词: Address; Age; Aging; Aging-Related Process; Biological Markers; Bypass; Caenorhabditis elegans; Cardiovascular Diseases; Cell Aging; Cells; Cellular Stress; Chromatin; Chromatin Remodeling Factor; Chromatin Structure; Chronic Disease; Complex; Coupled; DNA Damage; Data; Defense Mechanisms; Disease; Down-Regulation; Epigenetic Process; Fibroblasts; Formaldehyde; Genes; Genetic Transcription; Genetically Engineered Mouse; Genome Stability; Goals; Growth; Health; Heterochromatin; High-Throughput Nucleotide Sequencing; Histone H3; Histones; Human; Individual; Intervention; Knowledge; Lead; Life; Longevity; Lysine; Maintenance; Malignant Neoplasms; Mediating; Melanocytic nevus; Methylation; Methyltransferase; Mitochondria; Modification; Molecular; Monitor; Mutation; NADPH Oxidase; Nerve Degeneration; Neurodegenerative Disorders; Non-Insulin-Dependent Diabetes Mellitus; Normal tissue morphology; Oncogenes; Pathway interactions; Patients; Phenotype; Physiological Processes; Play; Polycomb; Premature aging syndrome; Process; Production; Progeria; Proteins; Reactive Oxygen Species; Regulatory Element; Reporting; Repression; Research; Risk Factors; Role; Series; Signal Pathway; Signal Transduction; Site; Stem cells; Syndrome; Telomere Shortening; Up-Regulation; Variant; Wound Healing; age related; base; body system; cancer cell; chromatin immunoprecipitation; gene repression; genome-wide; genome-wide analysis; histone methylation; human EZH2 protein; human morbidity; human mortality; improved; member; next generation; novel; overexpression; peroxisome; research study; response; senescence; single cell analysis; telomere; therapeutic target; tissue repair

DESCRIPTION (provided by applicant): Age is a major risk factor for many diseases including cancer, cardiovascular disease, neurodegeneration, and type II diabetes. Recent research has identified universal mechanisms that determine and regulate organismal aging, and impact all organ systems. Understanding the fundamental processes of aging is expected to provide therapeutic targets to delay the onset of many age-associated diseases. Emerging evidence suggests that cellular senescence contributes to the physiological process of organismal aging. Cellular senescence refers to the irreversible growth arrest that is triggered by telomere shortening and also by a variety of cellular stresses. The Polycomb group protein Enhancer of Zeste Homolog 2 (EZH2), a methyltransferase that catalyzes the tri-methylation of histone 3 at lysine 27 (H3K27me3), has been implicated in regulating cellular senescence. The long-term objective of my research is to understand the molecular processes that contribute to senescence. Specifically, I propose here a series of mechanistic experiments and genome-wide analyses to investigate the mechanisms by which EZH2 regulates cellular senescence. Aim 1 will examine the connections between EZH2 and the Wnt signaling pathway, a known regulator of cellular senescence, using knockdown and overexpression strategies. Aim 2 will investigate the mechanism by which repression of EZH2 triggers the increase in reactive oxygen species. Aim 3 will examine the changes in global chromatin structure that are triggered during senescence induced by the downregulation of EZH2. My studies will help define novel mechanisms by which epigenetic changes impact and regulate cellular senescence. This knowledge is expected to open new avenues for interventions to delay age-associated diseases and increase human health span.

描述（由申请人提供）：年龄是许多疾病的主要危险因素，包括癌症、心血管疾病、神经退行性疾病和II型糖尿病。最近的研究已经确定了决定和调节机体衰老的普遍机制，并影响所有器官系统。了解衰老的基本过程有望提供治疗靶点，以延缓许多与年龄相关的疾病的发作。新出现的证据表明，细胞衰老有助于机体衰老的生理过程。细胞衰老是指由端粒缩短和各种细胞应激引起的不可逆转的生长停滞。Polycomb group protein Enhancer of Zeste Homolog 2 （EZH2）是一种甲基转移酶，可催化组蛋白3在赖氨酸27 （H3K27me3）处的三甲基化，与调节细胞衰老有关。我研究的长期目标是了解导致衰老的分子过程。具体来说，我建议在这里进行一系列的机制实验和全基因组分析来研究EZH2调节细胞衰老的机制。目的1将使用敲低和过表达策略研究EZH2和Wnt信号通路之间的联系，Wnt信号通路是已知的细胞衰老调节因子。目的2将探讨抑制EZH2触发活性氧增加的机制。目的3将研究在EZH2下调诱导的衰老过程中引发的整体染色质结构的变化。我的研究将有助于定义表观遗传变化影响和调节细胞衰老的新机制。这一知识有望为延缓与年龄有关的疾病和延长人类健康寿命的干预措施开辟新的途径。