The Role of Histone H4 in Genome Stability

组蛋白 H4 在基因组稳定性中的作用

• 批准号: 7150600
• 负责人: M MITCHELL SMITH
• 金额: $ 29.82万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-01-01 至 2008-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7150600
• 关键词: Acetylation; Address; Area; Biological Assay; Cells; Chromatin Structure; Chromosome Structures; Classification; Complex; Condition; DNA Double Strand Break; DNA Microarray Chip; DNA Microarray format; DNA Repair; DNA Sequence; DNA biosynthesis; Defect; Dissection; Double Strand Break Repair; Ensure; Event; Face; Family; Gene Conversion; Gene Expression; Genes; Genetic; Genetic Screening; Genome; Genome Stability; Genomics; Growth; H2AFX gene; Histone Acetylation; Histone H4; Histones; Human; In Vitro; Kinetics; Lead; Licensing; Maintenance; Measures; Metabolic; Modeling; Modification; Molecular; Molecular Genetics; Mothers; Movement; Mutation; Nucleosomes; Pathway interactions; Phosphorylation; Play; Process; Protein Acetylation; Proteins; Proteomics; Replication Initiation; Replicon; Research; Role; Signal Pathway; Site; Source; Techniques; Temperature; Testing; Thinking; Work; Yeasts; carcinogenesis; daughter cell; design; functional genomics; genetic analysis; histone acetyltransferase; human H2AX protein; member; mutant; novel; reconstitution; repaired; research study; transmission process; tumor progression

DESCRIPTION (provided by applicant): Cells routinely encounter conditions that cause DNA double-strand breaks and defects in DNA replication-coupled events, both from external sources and as a result of normal metabolic activity. Maintaining DNA sequence stability in face of these challenges is essential for normal gene expression, chromosome organization, and faithful transmission of genetic information. Loss of genome stability, through defects in DNA replication or DNA damage repair, is thought to play a causative role in carcinogenesis and tumor progression. Both DNA replication and DNA damage repair must take place in the context of chromatin structure and there is increasing evidence that histone modifications are essential for these processes. We have discovered that acetylation of histone H4 by the NuA4 histone acetyltransferase complex is required for nonhomologous end-joining and replication-coupled double-strand break repair. Furthermore, both human HBO1 and yeast Esa1, members of the MYST family of histone acetyltransferases, play key roles in DNA replication. Little is known about the molecular mechanisms by which histone modifications participate in replication and repair functions. To address these issues we will focus on three major research questions: (1) how histone modification functions at the site of a double-strand break and the molecular steps that are defective in histone modification mutants; (2) the molecular role of acetylation in DNA replication initiation and elongation; and (3) the functional genomics of the histone-dependent pathways that maintain genome stability.

描述（由申请人提供）：细胞通常会遇到导致DNA复制偶联事件中DNA双链断裂和缺陷的条件，这些条件来自外部来源和正常代谢活动。面对这些挑战，保持DNA序列的稳定性对于正常的基因表达、染色体组织和遗传信息的忠实传递至关重要。基因组稳定性的丧失，通过DNA复制或DNA损伤修复的缺陷，被认为在致癌和肿瘤进展中起着致病作用。DNA复制和DNA损伤修复都必须在染色质结构的背景下进行，越来越多的证据表明组蛋白修饰对这些过程至关重要。我们已经发现，乙酰化组蛋白H4的NuA 4组蛋白乙酰转移酶复合物是所需的非同源末端连接和复制偶联双链断裂修复。此外，人类HBO 1和酵母Esa 1，组蛋白乙酰转移酶的MYST家族的成员，在DNA复制中发挥关键作用。关于组蛋白修饰参与复制和修复功能的分子机制知之甚少。为了解决这些问题，我们将集中在三个主要的研究问题：（1）组蛋白修饰如何在双链断裂的网站功能和分子步骤，是有缺陷的组蛋白修饰突变体;（2）乙酰化在DNA复制启动和延伸的分子作用;（3）功能基因组学的组蛋白依赖性途径，保持基因组的稳定性。