DNA Methylation and Gene Silencing in Arabidopsis

拟南芥中的 DNA 甲基化和基因沉默

• 批准号: 6968884
• 负责人: JUDITH L BENDER
• 金额: $ 30.66万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-07-01 至 2009-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6968884
• 关键词: Arabidopsis; DNA methylation; acetylation; chromatin immunoprecipitation; cytosine; double stranded RNA; gene deletion mutation; gene induction /repression; genetic screening; genetically modified plants; heterochromatin; histones; immunoprecipitation; isomerase; methyltransferase; nuclear runoff assay; plant genetics; polymerase chain reaction; small interfering RNA

DESCRIPTION (provided by applicant): In eukaryotes including mammals and plants, cytosine methylation and associated heterochromatin formation play a key role in regulating gene expression and genome integrity. Dysregulation of cytosine methylation contributes to human cancers and a number of genetic disorders. Cytosine methylation is also critical for the suppression of transposon expression and movement. We use a group of duplicated methylated endogenous genes in the laboratory plant Arabidopsis as a model system to study the establishment and maintenance of cytosine methylation and gene silencing. In this system, the methylation imprint is established by a double-stranded RNA (dsRNA)-based signal. This mode of methylation targeting was first elucidated in plants, but it is now clear that related mechanisms for RNA-directed heterochromatin formation occur in fungi and animals including mammals. As one aim of this proposal, we will further characterize the RNA signal for DMA methylation using a combination of genetic studies with RNA processing/binding mutants and molecular analysis of RNA, with a focus on understanding the role of short interfering RNAs (siRNAs) in guiding methylation patterning. As a second aim, we will use a novel genetic screen for factors that specifically maintain methylation at a dsRNA source locus. We have also determined that key factors for maintaining the RNA-directed DNA methylation imprint are a cytosine methyltransferase CMT3 and a histone H3 lysine 9 (K9) methyltransferase SUVH4/KYP. This relationship between cytosine methylation and histone H3 K9 methylation also occurs in fungal and mammlian systems. In the third aim of this proposal, we will characterize the stucture and function of SUVH4/KYP and partially redundant related SUVH proteins using biochemical, genetic, and transgenic approaches, with the long-term goal of understanding the connections between RNA, histone methylation, and DNA methylation.

描述（由申请人提供）：在包括哺乳动物和植物在内的真核生物中，胞嘧啶甲基化和相关的异染色质形成在调节基因表达和基因组完整性中起关键作用。胞嘧啶甲基化的失调有助于人类癌症和许多遗传疾病。胞嘧啶甲基化对于抑制转座子表达和运动也是至关重要的。我们利用拟南芥中一组重复甲基化的内源基因作为模型系统，研究胞嘧啶甲基化和基因沉默的建立和维持。在该系统中，甲基化印记通过基于双链RNA（dsRNA）的信号建立。这种甲基化靶向模式首先在植物中阐明，但现在很清楚，RNA指导的异染色质形成的相关机制发生在真菌和动物（包括哺乳动物）中。作为本提案的一个目标，我们将进一步表征DNA甲基化的RNA信号，使用RNA加工/结合突变体和RNA分子分析的遗传学研究相结合，重点是了解短干扰RNA（siRNA）在指导甲基化模式中的作用。作为第二个目标，我们将使用一种新的遗传筛选因子，特异性地维持dsRNA源基因座的甲基化。我们还确定了维持RNA指导的DNA甲基化印记的关键因素是胞嘧啶甲基转移酶CMT 3和组蛋白H3赖氨酸9（K9）甲基转移酶SUVH 4/KYP。胞嘧啶甲基化和组蛋白H3 K9甲基化之间的这种关系也发生在真菌和真菌系统中。在本提案的第三个目标中，我们将使用生物化学，遗传学和转基因方法表征SUVH 4/KYP和部分冗余相关SUVH蛋白的结构和功能，长期目标是了解RNA，组蛋白甲基化和DNA甲基化之间的联系。