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中文摘要
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描述(由申请人提供): 这项提议的长期目标是在孤立蛋白质-DNA复合体的水平上了解蛋白质的行为。这一提议利用了一种新的单分子方法,可以可视化蛋白质与DNA的单个复合体的行为和动态性质。我们将研究几种不同的蛋白质-DNA复合体,每个复合体都是DNA重组过程的重要组成部分。将要检测的蛋白质包括DNA链交换蛋白RecA和RAD51;RecA/RAD51功能的介体和调节物;以及最后的核蛋白和染色质重塑转位酶Rad54蛋白。具体目的是:1.可视化和测量RecA和RAD51核蛋白细丝的组装、拆解和极性。这一目标研究了RecA/RAD51核蛋白细丝的核心行为--它的动态行为和寻找DNA同源性的能力。2.确定竞争对手和介体如何改变RecA/RAD51核蛋白细丝的动态行为。这个目的是解决竞争蛋白、介体蛋白和马达蛋白如何调节RecA和RAD51细丝的行为的问题。3.明确Rad54蛋白沿dsDNA易位的作用。本研究的目的是探讨RAD54转位能力的功能及其重塑蛋白质-DNA复合体的能力。这些蛋白质在单分子水平上的实时可视化,为了解这些蛋白质的行为和功能提供了一个全新的窗口。这些蛋白质中的每一个都参与通过重组修复DNA断裂,这一过程的机制尚不完全清楚。最近,可视化这些修复酶在DNA单分子上的作用的新方法已经开发出来。这些方法可以对这些复杂的过程提供前所未有的理解。这些单分子方法将被用来定义一些分子事件,这些事件包括支持重组DNA修复的日益复杂的生化过程。 公共卫生相关性: 项目叙述基因重组是维持染色体完整性所必需的基本生物学过程。这项研究意义重大,因为它提供了有关蛋白质-蛋白质和蛋白质-DNA相互作用的基本信息,这些相互作用对于通过重组进行正常的DNA断裂修复是必不可少的。重组DNA断裂修复的一个主要功能是防止基因组重排。这些蛋白质负责在所有生物体中保持遗传完整性,当人类出现缺陷时,它们会导致各种疾病。如果不加以修复,这些DNA断裂可能会导致基因组不稳定,从而可能导致肿瘤发生。这些蛋白质在人类中的突变不仅会导致癌症的易感性,还会导致异常的减数分裂和胚胎死亡。了解这一过程的分子机制将有助于揭示导致染色体易位和基因组不稳定的异常生物事件。因此,对重组DNA修复的详细分子理解对人类健康非常重要。
英文摘要
DESCRIPTION (provided by applicant): The long-term objective of this proposal is to understand the behavior of proteins at the level of solitary protein-DNA complexes. This proposal takes advantage of a novel single-molecule approach that can visualize the behavior and dynamic properties of individual complexes of proteins with DNA. Several different protein-DNA complexes will be examined; each is an essential component of the DNA recombination process. The proteins that will be examined include the DNA strand exchange proteins, RecA and Rad51; the mediators and modulators of RecA/Rad51 function; and the finally the nucleoprotein- and chromatin-remodeling translocase, Rad54 protein. The specific aims are to: 1. Visualize and measure the assembly, disassembly, and polarity of RecA and Rad51 nucleoprotein filaments. This aim addresses the core behavior of the RecA/Rad51 nucleoprotein filament - its dynamic behavior and its ability to find DNA homology. 2. Determine how the dynamic behavior of RecA/Rad51 nucleoprotein filaments is modified by competitors and mediators. This aim addresses the question of how competitor, mediator, and motor proteins modulate the behavior of RecA and Rad51 filaments. 3. Define the role of translocation along dsDNA by Rad54 protein. This aim addresses the functions of Rad54 translocation capacity and its ability to remodel protein-DNA complexes. The visualization of these proteins acting at the single-molecule level, in real-time, affords a completely new window into the behavior and function of these proteins. Each of these proteins is involved in the repair of DNA breaks by recombination, a process whose mechanism is not fully understood. Recently, new methods of visualizing the action of these repair enzymes on single-molecules of DNA have been developed. These methods can provide an unprecedented level of understanding of these intricate processes. These single-molecule methods will be used to define some of the molecular events comprising increasingly complicated biochemical processes that underpin recombinational DNA repair. PUBLIC HEALTH RELEVANCE: Project Narrative Genetic recombination is a fundamental biological process that is necessary for the maintenance of chromosomal integrity. The research in this proposal is significant because it provides basic information about the protein-protein and protein-DNA interactions that are essential for normal DNA-break repair by recombination. A major function of recombinational DNA-break repair is the prevention of genomic rearrangement. These proteins are responsible for preserving genetic integrity in all organisms and, when defective in humans, are responsible for a variety of diseases. Left unrepaired, these DNA breaks can result in genomic instabilities that that might permit tumorigenesis. Mutations in the human counterparts of these proteins result not only in predispositions to cancer, but give rise to aberrant meiosis and embryonic lethality. Understanding the molecular mechanism of this process should shed light abnormal biological events that lead to chromosomal translocations and genome instability. Consequently, a detailed molecular understanding of recombinational DNA repair is important to human health.
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Functions of BRCA1 and RAD51 Paralogs in Genome Stability and Tumor Suppression via Homologous Recombination
  • 批准号:
    10565421
  • 项目类别:
  • 资助金额:
    $36.56万
  • 财政年份:
    2023
  • 负责人:
    Stephen Charles Kowalczykowski
  • 依托单位:
Single-molecule visualization and mechanisms of DNA recombination and intersecting DNA transactions
  • 批准号:
    10595678
  • 项目类别:
  • 资助金额:
    $80.25万
  • 财政年份:
    2019
  • 负责人:
    Stephen Charles Kowalczykowski
  • 依托单位:
Single-molecule visualization and mechanisms of DNA recombination and intersecting DNA transactions
  • 批准号:
    10374054
  • 项目类别:
  • 资助金额:
    $80.25万
  • 财政年份:
    2019
  • 负责人:
    Stephen Charles Kowalczykowski
  • 依托单位:
Single-molecule visualization and mechanisms of DNA recombination and intersecting DNA transactions
  • 批准号:
    9900833
  • 项目类别:
  • 资助金额:
    $81.16万
  • 财政年份:
    2019
  • 负责人:
    Stephen Charles Kowalczykowski
  • 依托单位:
海外基金