ANALYSIS OF COMBINATORIAL CIS-REGULATION IN SYNTHETIC AND GENOMIC PROMOTERS

合成和基因组启动子中组合顺式调控的分析

• 批准号: 8600698
• 负责人: Barak A Cohen
• 金额: $ 34.96万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-01-01 至 2015-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8600698
• 关键词: Address; Affect; Binding; Binding Sites; Biological Assay; Cells; Complex; Custom; DNA; DNA Sequence; DNA-Directed RNA Polymerase; Data; Disease; Functional RNA; Gene Expression; Gene Expression Profile; Gene Expression Regulation; Genes; Genome; Genomic DNA; Genomics; Goals; Growth and Development function; Hereditary Disease; Knowledge; Learning; Libraries; Location; Malignant Neoplasms; Measures; Modeling; Molecular; Nature; Nucleic Acid Regulatory Sequences; Pattern; Play; Positioning Attribute; Process; Property; Regulation; Regulatory Element; Role; Source; Specific qualifier value; Stem cells; System; TATA Box; Test Result; Testing; Thermodynamics; Time; Yeasts; base; cellular engineering; chromatin modification; combinatorial; design; empowered; genetic variant; insight; novel; physical process; promoter; public health relevance; research study; transcription factor

DESCRIPTION (provided by applicant): The long-term goal of this project is to understand the combinatorial rules that govern the interactions between transcription factor binding sites (TFBS). Through these rules, combinations of TFBS specify an enormous diversity of complex gene expression patterns. Normal growth and development depends on the tight control of TFBS over levels of gene expression in both time and space, and aberrant regulation of gene expression underlies many genetic diseases. Although much progress has been made identifying TFBS, and the transcription factors (TFs) that bind to them, much less is known about how TFBS interact with each other to generate specific patterns of gene expression. This lack of knowledge is manifested in the inability to predict the expression patterns specified by novel combinations of TFBS, and the inability to distinguish true regulatory regions in the genome from spurious clusters of TFBS. The proposal addresses these problems through experiments designed to unravel the mechanisms that govern TFBS interactions. Large libraries of simplified synthetic promoters will be constructed and assayed for expression and TF occupancy. The data from these libraries will be analyzed with a thermodynamic model that describes the physical interactions between TFBS, TFs and RNA polymerase. The models produced from synthetic promoters will be explicitly tested on genomic promoters. In Aim 1 this system will be used to study the extent to which the simple occupancy of TFBS by TFs determines complex patterns of gene expression. In Aim 2 the system will be extended to determine the effects of additional variables on combinatorial cis-regulation, including the strength of the TATA box, chromosomal location, and chromatin modifications. The successful completion of the aims of this proposal will result in a quantitative and molecular understanding of the rules underlying combinatorial cis-regulation. Such an understanding is necessary to empower biomedical applications, such as stem cell engineering, that are based on manipulating gene expression patterns. The results produced from this proposal will also help guide the annotation of the large regions of non-coding DNA in the genome that specify gene expression patterns. Finally, a clear understanding of TFBS interactions will help the identification and interpretation of disease causing genetic variants that affect cis-regulation.

描述（由申请人提供）：该项目的长期目标是了解控制转录因子结合位点（TFBS）之间相互作用的组合规则。通过这些规则，TFBS 的组合指定了复杂基因表达模式的巨大多样性。正常的生长发育依赖于TFBS对基因表达水平在时间和空间上的严格控制，而基因表达的异常调控是许多遗传疾病的基础。尽管在识别 TFBS 以及与其结合的转录因子 (TF) 方面已经取得了很大进展，但对于 TFBS 如何相互作用以产生特定的基因表达模式却知之甚少。这种知识的缺乏表现在无法预测 TFBS 的新组合指定的表达模式，以及无法区分基因组中真正的调控区域和虚假的 TFBS 簇。该提案通过旨在解开 TFBS 相互作用的控制机制的实验来解决这些问题。将构建简化合成启动子的大型文库并分析表达和 TF 占用情况。来自这些文库的数据将使用描述 TFBS、TF 和 RNA 聚合酶之间物理相互作用的热力学模型进行分析。由合成启动子产生的模型将在基因组启动子上进行明确测试。在目标 1 中，该系统将用于研究 TF 对 TFBS 的简单占据在多大程度上决定了基因表达的复杂模式。在目标 2 中，系统将被扩展以确定附加变量对组合顺式调节的影响，包括 TATA 盒的强度、染色体位置和染色质修饰。该提案目标的成功实现将导致对组合顺式调节背后的规则的定量和分子理解。这种理解对于基于操纵基因表达模式的生物医学应用（例如干细胞工程）是必要的。该提案产生的结果还将有助于指导基因组中指定基因表达模式的大片非编码 DNA 区域的注释。最后，对 TFBS 相互作用的清晰了解将有助于识别和解释影响顺式调节的致病遗传变异。