项目名称: 同型半胱氨酸经组蛋白和DNA甲基化相互作用调控ERO1α促内质网应激的分子机制
项目编号: No.81460079
项目类型: 地区科学基金项目
立项/批准年度: 2015
项目学科: 医药、卫生
项目作者: 贾绍斌
作者单位: 宁夏医科大学
项目金额: 49万元
中文摘要: 内质网应激(ERS)是同型半胱氨酸(Hcy)致动脉粥样硬化(As)的重要机制,ERO1α是内质网上调控蛋白质折叠的关键基因,前期研究发现同条件下不同基因高低甲基化并存,提示存在更深层次机制,组蛋白甲基化具有协同DNA甲基化调控基因转录的作用,但Hcy是否经组蛋白和DNA甲基化相互作用介导ERO1α调控ERS机制尚未阐明,因此拟复制HHcy模型,免疫荧光分析ERO1α的变化,在细胞中使其沉默予以验证,明确其在As中的作用;转染ERO1α干扰载体分析ERS关键基因的变化并定位,将ERO1α持续失活或激活突变体与启动子报告质粒共转染,揭示ERO1α对靶基因的调控作用;运用MeDIP-qPCR检测组蛋白和ERO1αDNA甲基化的水平,沉默LSD1以逆转组蛋白甲基化及5-氮杂胞苷阻断DNA甲基化,探讨各自平衡模式打破后,组蛋白和DNA甲基化相互作用对靶基因表达的调控机制,为As靶向治疗提供理论依据。
中文关键词: 同型半胱氨酸;内质网应激;内质网氧化还原酶-1α;组蛋白甲基化;DNA甲基化
英文摘要: Endoplasmic reticulum stress (ERS) play an important role in homocysteine (Hcy) induced atherosclerosis (As). ERO1α is a key regulator of protein folding in the endoplasmic reticulum. Our previous studies showed that coexisting hypermethylation with hypomethylation of different genes under the same condition, which suggests a more complex regulation mechanism. The histone methylation coordinating with the DNA methylation regulates gene transcription function, but the significance of histone and DNA methylation regulating of ERO1α in homocysteine-induced ER stress has not been elucidated. Therefore, after established HHcy model, we will detect ERO1α with immunofluorescence and verify the crucial role of ERO1α in atherosclerosis by siRNA.Then we will analyze key genes of ERS by transfecting interference vectors of ERO1α and mapping them , explore the role of ERO1α regulating its target genes using constitutively active- and dominant negative-plasmids of ERO1α. Finally, we will measure the methylation status of H3K9 and ERO1α by MeDIP-qPCR, confirm the coordination of histone and DNA methylation regulating ERO1α when methylation homeostasis disturbed by silencing LSD1 and DNA methylation inhibitor 5-azacytidine. We hope that these studies would provide important insights into the effect and mechanism of hyperhomocysteinemia, thus identifying novel targets for therapeutic interventions of atherosclerosis.
英文关键词: homocysteine;endoplasmic reticulum stress;ER oxidoreductin-1 alpha;histone methylation;DNA methylation