Etiology of Chromosome Translocations

染色体易位的病因学

基本信息

批准号：
7525898
负责人：
SANG EUN LEE
金额：
$ 25.68万
依托单位：
UNIVERSITY OF TEXAS HLTH SCIENCE CENTER
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-07-01 至 2012-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7525898
关键词：
Biochemical Genetics Biochemistry Biological Assay Biological Models Blood typing procedure Cell Cycle Checkpoint Cells Cellular biology Childhood Chromosomal Breaks Chromosomal translocation Chromosome abnormality Chromosomes Complex DNA DNA Damage DNA Double Strand Break DNA lesion Defect Detection Diagnosis Disease Double Strand Break Repair Etiology Fluorescence Microscopy Frequencies Gene Mutation Genes Genetic Genetic Screening Genome Goals H2AFX gene Hematopoietic Neoplasms Hereditary Disease Human Kinetics Light Malignant Childhood Neoplasm Malignant lymphoid neoplasm Mediating Medical Surveillance Modeling Molecular Monitor Nonhomologous DNA End Joining Oncogenic Pathway interactions Patients Phosphorylation Population Preventive Process Proteins Public Health Reaction Reciprocal Translocation Research Role Saccharomyces cerevisiae Sequence Analysis Signal Transduction Site System Techniques Therapeutic Time Treatment Protocols Yeasts base cancer type carcinogenesis cohesin genetic analysis human H2AX protein in vivo insight mutant novel outcome forecast prevent programs repaired response sarcoma time use

项目摘要

DESCRIPTION (provided by applicant): Chromosome translocations are frequently associated with many types of blood cancers and childhood sarcomas. Clinically, chromosome translocations are important because they offer the ability to precisely diagnose the type of cancers and to tailor treatment. Paradoxically, the molecular mechanism that leads to chromosome translocations is not well understood. The available evidence suggests the role of process repairing DNA double strand breaks in the formation of chromosome translocations. Recently, we developed a novel yeast-based model system to detect non-homologous end joining (NHEJ)- dependent, reciprocal chromosome translocations in vivo. This system allowed us to detect in real time a reciprocal translocation of site-specific DNA double strand breaks from a population of cells. A screen using our system resulted in the identification of several gene mutations that elevate the frequency of NHEJ- dependent chromosome translocations. Through this system, we uncovered a role of a specific DNA damage surveillance pathway in suppression of chromosome translocations. The focus of this proposal is to identify and characterize the genetic network that suppresses chromosome translocation. An approach combining genetics, cell biology and biochemistry will be used to provide mechanistic insights into genetic and mechanistic underpinnings of NHEJ-mediated chromosome translocations. These studies will shed light on the molecular mechanism leading to chromosome translocations in humans and may provide conceptual basis for advanced therapeutics to treat or prevent blood cancers. PUBLIC HEALTH RELEVANCE: The long-term objective of our research program is to dissect the molecular mechanism that causes oncogenic chromosome translocations. Mutations of genes identified by our study are known to enforce one of the DNA damage surveillance pathways, which can suppress chromosome translocations, and predispose patients to chromosomal translocations and lymphoid malignancy. This application will identify and characterize damage- surveillance and other mechanisms that suppress chromosome translocation to understand the defects in blood cancers and develop novel preventive and/or therapeutic strategies.

描述（由申请人提供）：染色体易位经常与多种类型的血癌和儿童肉瘤相关。在临床上，染色体易位很重要，因为它们提供了精确诊断癌症类型和定制治疗的能力。矛盾的是，导致染色体易位的分子机制尚不清楚。现有证据表明修复 DNA 双链断裂的过程在染色体易位形成中的作用。最近，我们开发了一种新型的基于酵母的模型系统，用于检测体内非同源末端连接（NHEJ）依赖的相互染色体易位。该系统使我们能够实时检测细胞群中特定位点 DNA 双链断裂的相互易位。使用我们的系统进行的筛选鉴定出了几个基因突变，这些突变提高了 NHEJ 依赖性染色体易位的频率。通过这个系统，我们发现了特定 DNA 损伤监测途径在抑制染色体易位中的作用。该提案的重点是识别和表征抑制染色体易位的遗传网络。结合遗传学、细胞生物学和生物化学的方法将用于提供 NHEJ 介导的染色体易位的遗传和机制基础的机制见解。这些研究将揭示导致人类染色体易位的分子机制，并可能为治疗或预防血癌的先进疗法提供概念基础。公共健康相关性：我们研究计划的长期目标是剖析导致致癌染色体易位的分子机制。我们的研究发现的基因突变已知会加强DNA损伤监测途径之一，该途径可以抑制染色体易位，并使患者易患染色体易位和淋巴恶性肿瘤。该应用将识别和表征损伤监测和其他抑制染色体易位的机制，以了解血癌的缺陷并开发新的预防和/或治疗策略。