Transcriptional Activation by Small RNA: Mechanism and Design Rules

小 RNA 的转录激活：机制和设计规则

• 批准号: 8328731
• 负责人: HAO LI
• 金额: $ 45.43万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-25 至 2014-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8328731
• 关键词: Address; Binding; Bioinformatics; Biological; Cells; Characteristics; Complex; Coupled; Disease; Double-Stranded RNA; Environment; Gene Activation; Gene Expression; Gene Expression Regulation; Gene Silencing; Gene Targeting; Genes; Genomics; Goals; Guide RNA; Life; Malignant Neoplasms; Mediating; Mediator of activation protein; Molecular; Molecular Biology; Molecular Machines; Nucleic Acids; Physiological; Process; Proteins; Public Health; RNA Interference; Sensitivity and Specificity; Small RNA; Transcriptional Activation; Transcriptional Regulation; cDNA Arrays; chromatin immunoprecipitation; design; gene function; gene therapy; improved; insight; promoter; public health relevance; tool

DESCRIPTION (provided by applicant): The goal of this application is to establish a new paradigm of gene regulation mediated by small RNA. Until recently, small RNAs have been thought to function mainly as the mediators of an evolutionally conserved gene silencing mechanism known as RNAi. We and others discovered that small double stranded RNA (dsRNA) targeting gene promoter sequence can induce potent and prolonged gene activation at the transcriptional level and in a sequence-specific manner, a phenomenon we termed RNAa. Despite the enormous potential for reprogramming gene expression in living cells, the molecular mechanism of RNAa is largely unknown and the rules for target selection are still quite obscure. We propose to use a combination of genomic, bioinformatic, and molecular biology approaches to address the following questions: How is transcriptional activation by promoter-targeted dsRNA achieved? What are the molecular machines involved? Is RNAa naturally exploited by cells for physiological function? What are the general rules governing the sensitivity and specificity of dsRNA-promoter targeting? Understanding the molecular mechanism of RNAa and establishing it as a new paradigm are likely to transform the way gene function is studied and diseases such as cancer are treated.

描述(申请人提供)：本申请的目标是建立一种由小RNA介导的新的基因调控范例。直到最近，小RNA一直被认为主要作为一种进化保守的基因沉默机制(RNAi)的中介。我们和其他人发现，靶向基因启动子序列的小双链RNA(DsRNA)可以在转录水平上以序列特异性的方式诱导有效和持久的基因激活，我们称之为RNAa。尽管在活细胞中重新编程基因表达的潜力巨大，但RNAa的分子机制在很大程度上是未知的，靶标选择的规则仍然相当模糊。我们建议使用基因组、生物信息学和分子生物学方法的组合来解决以下问题：如何实现启动子靶向dsRNA的转录激活？涉及到的分子机器是什么？RNAa是细胞天然利用的生理功能吗？控制dsRNA启动子靶向的敏感性和特异性的一般规则是什么？了解RNAa的分子机制并将其建立为一种新的范式，可能会改变研究基因功能和治疗癌症等疾病的方式。