Excision of Carcinogen-DNA Adducts in Nucleosomes

核小体中致癌物-DNA 加合物的切除

• 批准号: 8520270
• 负责人: Nicholas E Geacintov
• 金额: $ 30.24万
• 依托单位: NEW YORK UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-08-01 至 2017-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8520270
• 关键词: Accounting; Adenine; Advanced Malignant Neoplasm; Affect; Air; Animal Model; Area; Aromatic Polycyclic Hydrocarbons; Attention; Bay Region; Benzo(a)pyrene; Binding Sites; Biological; Biological Assay; Biological Markers; Biological Models; Cancer Etiology; Carcinogens; Cell Extracts; Cells; Chromatin; Communities; DNA; DNA Adducts; DNA Packaging; DNA Repair; DNA lesion; Development; Environment; Environmental Carcinogens; Environmental Exposure; Epoxy Compounds; Etiology; Excision; Fluorescence Resonance Energy Transfer; Food; Fossil Fuels; Future; Glycols; Guanine; Health; Hela Cells; Histone H2B; Histone H3; Histones; Human; Hybrids; Individual; Investigation; Laboratory Research; Lesion; Libraries; Liquid substance; Lung; Malignant Neoplasms; Mammalian Cell; Methods; Modeling; Modification; Molecular; Mutagens; NURF; Nucleosomes; Nucleotide Excision Repair; Outcome Study; Population; Positioning Attribute; Predisposition; Prevention approach; Process; Property; Proteins; Recombinants; Relative (related person); Resistance; Role; Site; Smoker; Structure; System; Therapeutic Agents; Thermodynamics; Time; Tissues; Tobacco smoke; Variant; Water; adduct; aqueous; base; cancer prevention; chemical carcinogen; chemical carcinogenesis; chromatin remodeling; design; environmental chemical; exhaust; hazard; histone modification; human tissue; in vivo; insight; interest; molecular dynamics; next generation; non-smoker; novel; prototype; reconstitution; repaired; research study; tumorigenic

DESCRIPTION (provided by applicant): Polycyclic aromatic hydrocarbons (PAH) are byproducts of fossil fuel combustion and are present in our air, food and water; the presence of these genotoxic environmental carcinogens in our environment continues to be a hazard to human health. The structural features and biological impact of PAH that distinguish highly active mutagens and tumorigens from structurally related less active, or inactive compounds, have long been of interest for understanding the etiology of human cancers in exposed populations. There are two important sub-classes of PAH that are distinguished by different topological features: (i) the sterically hindered 'fjord' region that causes significant non-planarity in the aromatic ring system of fjord PAH, and (ii) 'bay' region PAH that are sterically unhindered and planar (e.g., the well known environmental carcinogen benzo[a]pyrene). Both types of PAH are metabolically activated to reactive diol epoxide intermediates that react predominantly with guanine and adenine in cellular DNA to form pre-mutagenic covalent adducts in mammalian cells and tissues that can, if not repaired, ultimately contribute to the etiology of human cancers The fjord PAH have attracted significant attention by the chemical carcinogenesis community because they are up to ~ 100-fold more tumorigenic than the bay region prototype benzo[a]pyrene. Previous research from this laboratory has shown that there are remarkable differences in the relative excision efficiencies of different, stereochemically well defined PAH-DNA adducts by the human nucleotide excision repair (NER) system in whole cell extracts. Of particular interest are the observations that PAH- adenine DNA adducts derived from highly tumorigenic fjord PAH are strongly resistant to NER. However, these conclusions are built on NER experiments that were conducted with free DNA in aqueous environments; it is not known whether in biologically more relevant protein environments of nucleosomes, the fundamental sub-units of DNA packaging in the cell, similar hierarchies of NER will be observed with DNA substrates containing the same single bay and fjord PAH-DNA adducts. The objectives of this project are to evaluate NER efficiencies in nucleosomal DNA. The specific aims are: (1) to investigate the role of DNA positioning sequence, thermodynamic stability, nucleosome dynamics, and accessibility of DNA adducts at different sites of the nucleosomal superhelix on NER efficiencies; (2) Evaluate the effects of covalent modification of H3, H4, H2A and H2B histones on the same nucleosome properties and NER; (3) Determine how structurally distinct fjord and bay region PAH-DNA adducts in nucleosomes are differentially excised by the NER system with human cell extracts in nucleosomes, and elucidate how the excision efficiencies are impacted by the histone environment compared with uncomplexed DNA The outcome of this study is expected to provide a molecular basis for future investigations of how bulky carcinogen-DNA lesions are processed in vivo and how nucleosome remodeling factors enhance and facilitate the NER of bulky DNA lesions in cellular environments.

描述(申请人提供)：多环芳烃(PAH)是化石燃料燃烧的副产品，存在于我们的空气、食物和水中；这些具有遗传毒性的环境致癌物质在我们的环境中的存在继续对人类健康构成危害。多环芳烃的结构特征和生物学影响将高活性诱变剂和致癌物与结构相关的不太活性或非活性化合物区分开来，长期以来一直是了解暴露人群中人类癌症病因学的兴趣所在。多环芳烃有两个重要的亚类，它们通过不同的拓扑特征来区分：(I)导致峡湾多环芳烃芳环体系显著非平面性的空间受阻‘Fjord’区域，和(Ii)空间无阻碍且平面的‘Bay’区域PAH(例如，众所周知的环境致癌物质苯并[a]芘)。这两种类型的多环芳烃都被代谢激活为反应性的二醇环氧化物中间体，这些中间体主要与细胞DNA中的鸟嘌呤和腺嘌呤反应，在哺乳动物细胞和组织中形成诱变前的共价加合物，如果不修复，这些加合物可能最终导致人类癌症的发生。峡湾多环芳烃引起了化学致癌界的极大关注，因为它们的致瘤性比湾区原型苯并[a]芘高100倍。该实验室以前的研究表明，在全细胞提取液中，通过人类核苷酸切除修复(NER)系统，不同立体化学定义明确的PAH-DNA加合物的相对切割效率存在显著差异。特别令人感兴趣的是观察到来自高度致癌的峡湾PAH的PAH-腺嘌呤DNA加合物对NER具有很强的抗性。然而，这些结论是建立在水环境中用游离DNA进行的NER实验基础上的；目前尚不清楚，在生物学上更相关的核小体蛋白质环境中，核小体是DNA包装的基本亚单位，在含有相同单海湾和峡湾PAH-DNA加合物的DNA底物上是否会观察到类似的NER层次结构。该项目的目标是评估核小体DNA中NER的效率。其具体目的是：(1)研究DNA定位序列、热力学稳定性、核小体动力学和DNA加合物在核小体超螺旋不同位置的可及性对NER效率的影响；(2)评价H3、H4、H_2A和H_2B组蛋白的共价修饰对相同的核小体性质和N ER的影响；(3)确定核小体中结构不同的峡湾和湾区PAH-DNA加合物如何被NER系统与核小体中的人细胞提取物进行差异切割，并阐明与未复合DNA相比，组蛋白环境对切割效率的影响。本研究结果有望为未来研究大型致癌物-DNA损伤在体内如何处理以及核小体重塑因子如何增强和促进细胞环境中大型DNA损伤的NER提供分子基础。