Ku regulates non-homologous end joining pathways in human somatic cells

Ku 调节人类体细胞中的非同源末端连接途径

• 批准号: 8820471
• 负责人: ERIC A HENDRICKSON
• 金额: $ 1.89万
• 依托单位: UNIVERSITY OF MINNESOTA
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-07 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8820471
• 关键词: Address; Affect; Applications Grants; Belief; Binding; Biological Assay; Cancer Patient; Cell Line; Cells; Chemicals; Chromosomal Breaks; Chromosomal Rearrangement; Clinical; Complex; DNA; DNA Damage; DNA Double Strand Break; DNA Repair; DNA ligase III; Defect; Development; Double Strand Break Repair; Ensure; Event; Fertility; Frequencies; G22P1 gene; Gene Mutation; Gene Targeting; Generations; Genes; Genetic; Genetic Recombination; Genome; Goals; Health; Homeostasis; Homologous Gene; Human; Human Cell Line; Human Genome; Immune; Immune system; Investigation; Ionizing radiation; Knowledge; Laboratories; Left; Lesion; Maintenance; Malignant Neoplasms; Measures; Mediating; Meiosis; Metabolism; Minor; Mission; Modality; Molecular; Nonhomologous DNA End Joining; Nucleotides; Null Lymphocytes; Oncogenic; Organism; Outcome; Pathway interactions; Patients; Positioning Attribute; Predisposition; Process; Publishing; Radiation; Radiation induced damage; Radiation induced double strand break; Radiation therapy; Recording of previous events; Reliance; Rodent; Signal Transduction; Sister Chromatid; Somatic Cell; Syndrome; System; Systems Development; Testing; Therapeutic; Tumor Tissue; United States National Institutes of Health; Up-Regulation; Work; cell killing; chemotherapy; cost; design; gene repair; genetic analysis; homologous recombination; human DNA; inhibitor/antagonist; insight; loss of function; loss of function mutation; mutant; neoplastic cell; novel; positional cloning; repaired; research study; response; telomere; tumor

DESCRIPTION (provided by applicant): We propose to study the impact of loss-of-function mutations of DNA DSB (double-strand break) repair genes on end joining processes in human cells. We will focus heavily, but not exclusively, on the heterodimeric (Ku70 and Ku86 subunits) Ku DNA end-binding complex and LIGIII (DNA ligase III). Ku has a storied history and it has been known for decades that it is required for most of the generalized DSB repair occurring in somatic cells as well as being critical for the proper development of the vertebrate immune system. Ku performs these duties as part of a repair pathway referred to as C-NHEJ (classic-non-homologous end joining). In work published this year, we demonstrated that Ku has a hitherto underappreciated function as a suppressor of the other competing DSB repair pathways, namely A-NHEJ (alternative-NHEJ) and HR (homologous recombination). Thus, when the levels of Ku are reduced, A-NHEJ and HR, which normally comprise only a small fraction of the end joining activity in human cells, become more active. This observation has potential clinical implications. Thus, the vast majority of human cancer patients are treated either with radio- or chemotherapy (or both) and the efficacy of these anti-tumor modalities resides in their ability to generate DNA DSBs. Thus, strategies designed to increase the efficacy of tumor cell killing by radio- or chemotherapy that involve reducing the levels of Ku are likely to fail due to the up-regulation of A-NHEJ and/or HR. This is a hypothesis that we will directly test in this grant application. Moreover, the molecular mechanism by which Ku mediates this suppression is unknown and we propose genetic and reverse genetic experiments to elucidate this process. Finally, we have begun to genetically tackle the A-NHEJ pathway. A number of genes have been implicated in A-NHEJ, but the important genes remain poorly defined. One of the more compelling A- NHEJ candidates is LIGIII (DNA ligase III). To experimentally test the importance of LIGIII we have constructed a viable LIGIII-null human cel line and herein propose to characterize the impact of the loss-of- function of LIGIII on A-NHEJ. In particular, one characterization involves a novel and powerful assay system by which we can measure ionizing radiation-induced gross chromosomal rearrangements in human cells lacking LIGIII (or Ku86). To our knowledge, we are one of only a few laboratories in the world utilizing genetic, loss-of-function approaches to study DNA DSB in human cells and thus we are well positioned to gain insights into the mechanism of DSB repair that cannot be obtained elsewhere.

描述（由申请人提供）：我们建议研究DNA双链断裂修复基因的功能缺失突变对人类细胞末端连接过程的影响。我们将重点关注（但不限于）异二聚体（Ku70和Ku86亚基）Ku DNA末端结合复合物和LIGIII （DNA连接酶III）。Ku有一个传奇的历史，几十年来人们已经知道，它是大多数发生在体细胞中的广义DSB修复所必需的，也是脊椎动物免疫系统正常发育的关键。Ku作为C-NHEJ（经典非同源末端连接）修复途径的一部分履行这些职责。在今年发表的研究中，我们证明Ku具有迄今为止未被充分认识的功能，可以抑制其他竞争的DSB修复途径，即a - nhej（替代nhej）和HR（同源重组）。因此，当Ku水平降低时，通常只占人类细胞末端连接活性一小部分的a - nhej和HR变得更加活跃。这一观察结果具有潜在的临床意义。因此，绝大多数人类癌症患者要么接受放疗，要么接受化疗（或两者兼而有之），这些抗肿瘤方式的有效性取决于它们产生DNA dsb的能力。因此，旨在通过放疗或化疗提高肿瘤细胞杀伤效果的策略，包括降低Ku水平，很可能由于A-NHEJ和/或HR的上调而失败。我们将在本次拨款申请中直接检验这一假设。此外，Ku介导这种抑制的分子机制尚不清楚，我们提出了遗传和反向遗传实验来阐明这一过程。最后，我们已经开始从基因上解决A-NHEJ途径。许多基因与A- nhej有关，但重要的基因仍不明确。一个更引人注目的A- NHEJ候选者是LIGIII （DNA连接酶III）。为了实验验证LIGIII的重要性，我们构建了一个liiii缺失的人细胞系，并在此提出表征liiii功能缺失对a - nhej的影响。特别地，其中一个表征涉及一种新颖而强大的测定系统，通过该系统，我们可以测量电离辐射诱导的缺乏LIGIII（或Ku86）的人类细胞的总体染色体重排。据我们所知，我们是世界上仅有的几个利用基因、功能丧失方法研究人类细胞中DNA DSB的实验室之一，因此我们有能力深入了解其他地方无法获得的DSB修复机制。