Characterization of DNA N6-methyl adenine and its role in epigenetic memory

DNA N6-甲基腺嘌呤的表征及其在表观遗传记忆中的作用

• 批准号: 10001093
• 负责人: Eric Lieberman Greer
• 金额: $ 0.12万
• 依托单位: BOSTON CHILDREN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-09-30 至 2021-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10001093
• 关键词: Adenine; Appearance; Behavioral; Caenorhabditis elegans; Chromatin; Chromatin Structure; Complex; DNA; DNA Methylation; DNA Modification Process; Energy Metabolism; Enzymes; Epigenetic Process; Eukaryota; Excision; Foundations; Generations; Genetic Transcription; Genomics; Health; Hereditary Disease; Heritability; Human; Label; Location; Longevity; Memory; Metabolic; Methylation; Modification; Molecular; Nematoda; Organism; Phenotype; Positioning Attribute; Process; Purines; Regulation; Research; Role; System; Tissues; Work; demethylation; epigenetic memory; epigenetic regulation; non-genetic; novel; public health relevance; transgenerational epigenetic inheritance; zygote

Abstract Non-genetic information has recently been shown to regulate an increasing number of complex phenotypes, including physical appearance, energy metabolism, behavioral state, and longevity. How epigenetic information is transmitted from generation to generation is still largely unknown. Anything in the zygote, which is not the DNA itself, could carry this non-genetic information. Here we propose taking advantage of the nematode C. elegans, where we have characterized several examples of transgenerational epigenetic inheritance, to identify the heritable material that regulates epigenetic memory. We have identified that C. elegans contain an ancient form of DNA methylation, on the 6th position of the purine ring in adenines (6mA), which was previously thought to only occur in unicellular organisms. We were the first to identify this methylation in Metazoa and additionally found that this modification increases progressively in a paradigm of epigenetic memory. Here we propose to characterize this novel epigenetic modification in eukaryotes by identifying in which specific tissues and genomic locations 6mA modifications occur. We will also identify and characterize the enzymes that add, remove and recognize this modification. Finally we will combine metabolic methyl-labeling and directed methylation and demethylation to determine whether 6mA is the heritable material. Together this application will define a fundamental new layer of conserved epigenetic regulation and begin to identify whether 6mA can transmit a molecular memory across generations.

摘要