Epigenetic regulations of DNA and histone methylation and deMethylation: Structures and Mechanisms

DNA 和组蛋白甲基化和去甲基化的表观遗传调控：结构和机制

• 批准号: 10318519
• 负责人: Xiaodong Cheng
• 金额: $ 58.48万
• 依托单位: UNIVERSITY OF TX MD ANDERSON CAN CTR
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-01-01 至 2024-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10318519
• 关键词: Biochemical; Brain; Cell Differentiation process; Cytosine; DNA; DNA Methylation; DNA Methylation Regulation; DNA Modification Methylases; DNA Modification Process; Development; Dioxygenases; Enzymes; Epigenetic Process; Event; Fetus; Gene Expression; Generations; Genome; Genomics; Germ Lines; Lead; Light; Maintenance; Mammalian Cell; Mammals; Modification; Molecular; Positioning Attribute; Proteins; Reaction; Role; Series; Structure; T cell differentiation; demethylation; epigenetic memory; epigenetic regulation; histone methylation; oxidation; programs; transcription factor; young adult

Summary/Abstract The control of gene expression in mammals relies in part on modifications to cytosine residues in DNA, which exist in at least five forms: cytosine (C), 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC), 5- formylcytosine (5fC) and 5-carboxylcytosine (5caC). DNA methyltransferases methylate cytosine at the 5- position, generating 5mC in the genome. Ten-eleven translocation (Tet) dioxygenases convert 5mC to 5hmC, 5fC, and 5caC in three consecutive oxidation reactions. These modifications are dynamically regulated during development and cell differentiation. To understand the function of these modifications and the regulatory mechanisms that control the levels and genomic distribution of the five forms of the cytosine, we propose to study the enzymes/proteins that generate, read, and remove these DNA modifications as well as associated histone methylation.

摘要/摘要 哺乳动物中基因表达的控制部分依赖于DNA中胞嘧啶残基的修饰， 存在至少五种形式：胞嘧啶（C）、5-甲基胞嘧啶（5 mC）、5-羟甲基胞嘧啶（5 hmC）、5-甲基胞嘧啶（5 hm 甲酰胞嘧啶（5 fC）和5-羧基胞嘧啶（5caC）。DNA甲基转移酶甲基化胞嘧啶在5- 位置，在基因组中产生5 mC。10 - 11易位（泰特）双加氧酶将5 mC转化为5 hmC， 5 fC和5caC在三个连续的氧化反应。这些修改在过程中被动态地调节。 发育和细胞分化。为了了解这些修饰的功能和调控机制， 控制胞嘧啶的五种形式的水平和基因组分布的机制，我们建议 研究产生，读取和去除这些DNA修饰以及相关的酶/蛋白质 组蛋白甲基化