STUDIES OF NUCLEOSOME STABILITY AND TRANSCRIPTION

核小体稳定性和转录的研究

• 批准号: 6386596
• 负责人: MICHELLE D. WANG
• 金额: $ 26.25万
• 依托单位: CORNELL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-07-01 至 2004-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6386596
• 关键词: DNA; DNA directed RNA polymerase; acetylation; biophysics; cell component structure /function; chemical stability; chromatin; genetic transcription; histones; intermolecular interaction; microcapsule; nanotechnology; nucleosomes

Biological organisms must compactly store and yet efficiently read the huge amounts of genetic information contained in their DNA. Many DNA-based enzymes involved in these processes function as highly processive molecular motors capable of translocating over thousands of base pairs without detaching from the DNA template. These motors face mechanical obstacles to their movement, especially in the highly packed DNA of chromatin, and many of these obstacles are known to be important regulators of gene expression. The broad goal of this proposal is to address the question of how these DNA-based motors deal with these obstacles. DNA in chromatin is highly compact as compared to naked DNA. The primary packing unit of chromatin, the nucleosome, consists of roughly two turns of DNA wrapped around a core histone octamer. The molecular mechanism by which RNA polymerase deals with nucleosomes during transcription is not fully understood at the molecular level and remains one of the most fundamental questions in biology. We propose a unique, single-molecule, biophysical approach to address the question of how RNA polymerase deals with nucleosomes. The proposed method combines optical trapping with nanometer-precision position detection techniques, and complements ongoing biochemical and structural studies. This approach, which has proven to be a powerful tool for the study of transcription on naked DNA, will provide direct measurements and visualization of individual molecular events of transcription in chromatin in vitro. Two specific aims are proposed: (1) mechanical stability of DNA associated with nucleosomes, and (2) transcription through nucleosomes. Aim number 1 determines the strength of histone-DNA interactions by stretching a nucleosomal DNA from end-to-end and measuring the tension required to disrupt the nucleosomes. Aim number 2 makes a direct observation of the fate of a nucleosome during an encounter with a transcribing RNA polymerase by monitoring the movement of single molecules of RNA polymerase during transcription and simultaneously detecting possible nucleosome disruption events. Using these methods, we will determine the effects of histone acetylation and chromatin remodeling complexes on transcription through nucleosomal DNA. This proposed basic research will help to elucidate the mechanisms of transcription in eukaryotes, and will further establish the technical foundation for mechanical studies of other nucleic acid-based molecular motors at the single molecule level.

生物有机体必须紧凑地存储并高效地读取其DNA中包含的大量遗传信息。参与这些过程的许多基于DNA的酶作为高度进行性的分子马达发挥作用，能够在不脱离DNA模板的情况下转移超过数千个碱基对。这些马达在运动中面临机械障碍，特别是在高度堆积的染色质DNA中，其中许多障碍被认为是基因表达的重要调节因素。这项提案的主要目标是解决这些基于DNA的马达如何处理这些障碍的问题。与裸露DNA相比，染色质中的DNA高度致密。染色质的主要包装单位是核小体，它由大约两个包裹在核心组蛋白八聚体周围的DNA组成。RNA聚合酶在转录过程中处理核小体的分子机制在分子水平上还没有完全被理解，仍然是生物学中最基本的问题之一。我们提出了一种独特的、单分子的生物物理方法来解决RNA聚合酶如何处理核小体的问题。提出的方法结合了光学捕获和纳米精度的位置检测技术，并补充了正在进行的生化和结构研究。这一方法已被证明是研究裸DNA转录的有力工具，它将提供对体外染色质中单个转录分子事件的直接测量和可视化。提出了两个特定的目标：(1)与核小体相关的DNA的机械稳定性；(2)通过核小体转录。目的1通过端到端拉伸核小体DNA并测量破坏核小体所需的张力来确定组蛋白-DNA相互作用的强度。目的2通过监测转录过程中RNA聚合酶单分子的运动，同时检测可能的核小体破坏事件，直接观察核小体在遇到转录RNA聚合酶时的命运。利用这些方法，我们将通过核小体DNA来确定组蛋白乙酰化和染色质重塑复合体对转录的影响。这一基础研究将有助于阐明真核生物的转录机制，并将进一步为在单分子水平上研究其他基于核酸的分子马达奠定技术基础。