Structural Motifs in RNA

RNA 中的结构基序

• 批准号: 7496642
• 负责人: Howard Y Chang
• 金额: $ 41.33万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-18 至 2010-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7496642
• 关键词: Address; Algorithms; Binding; Biochemical; Biochemistry; Biological; Biological Process; Cessation of life; Class; Code; Complement; Complex; Complex Mixtures; Computing Methodologies; DNA; DNA Sequence; Data Set; Depth; Development; Diagnosis; Dictionary; Disease; Elements; Emerging Technologies; Exhibits; Fractionation; Functional RNA; Funding; Gene Expression; Gene Expression Profile; Gene Expression Regulation; Genes; Genetic Transcription; Genome; Genomics; Goals; Heart; Heterogeneous Nuclear RNA; Human; Indium; Intervention; Life; Light; Maps; Measurement; Mediating; Methodology; Methods; Modeling; Problem Solving; Proteins; RNA; RNA Biochemistry; RNA Decay; RNA Folding; RNA Transport; RNA-Binding Proteins; Regulation; Research; Research Personnel; Resolution; Sensitivity and Specificity; Series; Speed; Statistical Models; Structure; Techniques; Technology; Testing; Time; Transcriptional Regulation; Translations; Untranslated RNA; Untranslated Regions; Validation; Yeasts; base; cell growth; combinatorial; computerized tools; experimental analysis; functional genomics; genetic regulatory protein; human disease; insight; mRNA Precursor; programs; research study; stem; tool; transcription factor

DESCRIPTION (provided by applicant): Proper control of gene expression is essential for life. While substantial advances have been made in the discovery of DNA sequences and transcription factors that act combinatorial to regulate transcription, much less is known about later steps in the gene expression program. Nevertheless, it is now clear that substantial regulation and gene expression occurs post-transcriptional, in pre-mRNA splicing, RNA transport, RNA localization, translation, and RNA decay, and in the coordination of RNAs by RNA binding proteins (RBPs). Further, recent findings of widespread transcription of noncoding RNAs (ncRNA) and of the involvement of these RNAs in critical biological processes such as development and gene regulation suggest the existence of important classes of regulatory RNAs that we are just beginning to explore. The long term goal of this project is to develop tools that enable structural characterization of RNAs on a genome-wide scale. First, we will develop computational methods to delineate functional motifs in RNA based on predicted secondary structures. Second, we will develop high-throughput methodologies of mapping secondary and tertiary structures in RNA using a series of RNA footprinting techniques and high resolution tiling array technology. Third, we will develop computational and experimental methods to assign biological functions to RNA motifs and to validate them. This integrated pipeline of new experimental and computational tools will enable investigators to identify and decode regulatory RNA elements in the genome with unprecedented speed and precision. The control of gene expression lies at the heart of understanding fundamental biological processes, such as cell growth, differentiation, and death. A deep and comprehensive understanding of the gene expression program would help to reveal the mechanisms of many human diseases exhibiting faulty gene expression, and allow their diagnosis and intervention with newfound precision.

描述（由申请人提供）：基因表达的适当控制对生命至关重要。虽然在发现DNA序列和转录因子组合调节转录方面取得了重大进展，但对基因表达程序中的后续步骤知之甚少。然而，现在清楚的是，大量的调控和基因表达发生在转录后，在前mRNA剪接，RNA转运，RNA定位，翻译和RNA降解，并在RNA的协调RNA结合蛋白（RBP）。此外，最近的发现广泛的非编码RNA（ncRNA）的转录和参与这些RNA在关键的生物过程，如发展和基因调控表明存在的重要类别的调控RNA，我们才刚刚开始探索。该项目的长期目标是开发能够在全基因组范围内对RNA进行结构表征的工具。首先，我们将开发计算方法来描绘基于预测的二级结构的RNA中的功能基序。第二，我们将开发高通量的方法，映射二级和三级结构的RNA使用一系列的RNA足迹技术和高分辨率平铺阵列技术。第三，我们将开发计算和实验方法来分配RNA基序的生物功能，并验证它们。这种新的实验和计算工具的集成管道将使研究人员能够以前所未有的速度和精度识别和解码基因组中的调控RNA元件。 基因表达的控制是理解基本生物过程的核心，如细胞生长，分化和死亡。对基因表达程序的深入而全面的理解将有助于揭示许多表现出错误基因表达的人类疾病的机制，并使其诊断和干预具有新的精确度。