Role of Linker Histone H1 in Epigenetic Gene Regulation

连接组蛋白 H1 在表观遗传基因调控中的作用

• 批准号: 7507071
• 负责人: YUHONG FAN
• 金额: $ 27.7万
• 依托单位: GEORGIA INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-08-01 至 2013-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7507071
• 关键词: Address; Adult; Affect; Binding; Cell Differentiation process; Cells; Chromatin; Chromatin Structure; DNA; DNA Methylation; DNA Methyltransferase; DNA Modification Methylases; Dependence; Development; Disease; ES Cell Line; Embryo; Embryonic Development; Epigenetic Process; Event; Gametogenesis; Gene Expression; Gene Expression Regulation; Genes; Genome; Genomic Imprinting; Germ Layers; Goals; H19 gene; Higher Order Chromatin Structure; Histone H1; Histone H1(s); Histones; Knock-out; Knowledge; Link; Maintenance; Malignant Neoplasms; Mammals; Mediating; Modification; Mus; Nuclear; Nucleosome Core Particle; Organism; Pattern; Play; Pregnancy; Process; Protein Family; Proteins; Purpose; Regulation; Role; SPT6 Protein; Study models; System; Testing; Therapeutic; Tissues; X Inactivation; cell type; embryonic stem cell; human disease; imprint; in vivo; methylcobalamin-coenzyme M methyltransferase; mouse model; novel; therapeutic target

DESCRIPTION (provided by applicant): Role of Linker Histone H1 in Epigenetic Gene Regulation Project Summary Epigenetic mechanisms are crucial for chromatin structure reprogramming and gene expression during mammalian development and cell differentiation. H1 linker histones are major chromatin structural proteins that associate with nucleosome core particles and play a key role in mediating higher order chromatin structure folding. However, the role of H1 in epigenetic gene regulation has not been explored. Previously we showed, by inactivating 3 H1 linker histone genes simultaneously, that the total amount of H1 is essential for mammalian development. We derived triple H1 null embryonic stem cell lines and showed that H1 is particularly important in controlling several imprinted gene expression in these cells. We also found that DNA methylation level at the imprinting control regions of these two affected loci is decreased with H1 reduction, thus suggesting a new link between H1 and DNA methylation. We now propose to address the underlying mechanisms of this novel epigenetic link and to investigate additional H1 regulated epigenetic events in embryonic stem cells and in mouse models. Specifically, we will: 1) Test whether H1 histones regulate establishment or maintenance of specific DNA methylation patterns through recruitment of DNA methyltransferases; 2) Identify additional critical H1 regulated epigenetic events and characterize the sequence and functional dependence of such events that are required for proper control of gene expression; 3) Study the in vivo regulatory role of H1 in epigenetic gene regulation during embryogenesis and gametogenesis. Findings from these studies will advance our knowledge of epigenetic gene regulation mechanisms. Relevance: Aberrant epigenetic gene regulation has been responsible for many human diseases, such as cancer and imprinted gene diseases. Understanding the epigenetic gene regulation mechanisms will provide critical clues as to how the epigenetic information can be experimentally reprogrammed for therapeutic purposes.

描述(由申请人提供)：连接者组蛋白H1在表观遗传基因调控项目中的作用概述表观遗传机制在哺乳动物发育和细胞分化过程中对染色质结构重新编程和基因表达至关重要。H1连接体组蛋白是与核小体核心颗粒结合的主要染色质结构蛋白，在介导高阶染色质结构折叠中起着关键作用。然而，H1在表观遗传基因调控中的作用还没有被探索。以前，我们通过同时失活3个H1连接蛋白基因，证明了H1的总量对哺乳动物的发育是必不可少的。我们获得了三个H1缺失的胚胎干细胞系，并表明H1在控制这些细胞中的几个印记基因表达方面特别重要。我们还发现，这两个受影响的基因座印迹控制区的DNA甲基化水平随着H1的减少而降低，从而表明H1和DNA甲基化之间存在新的联系。我们现在建议解决这种新的表观遗传联系的潜在机制，并在胚胎干细胞和小鼠模型中研究额外的H1调节的表观遗传事件。具体地说，我们将：1)测试H1组蛋白是否通过招募DNA甲基转移酶来调控特定DNA甲基化模式的建立或维持；2)识别其他关键的H1调控的表观遗传事件，并表征这些事件的序列和功能依赖性，这些事件是适当控制基因表达所必需的；3)研究H1在胚胎发生和配子发生过程中表观遗传基因调控中的体内调控作用。这些研究的发现将促进我们对表观遗传基因调控机制的了解。相关性：异常的表观遗传基因调控导致了许多人类疾病，如癌症和印记基因疾病。了解表观遗传基因调控机制将为如何通过实验重新编程表观遗传信息以达到治疗目的提供关键线索。