Environmental Toxicology Using Transgenic Models

使用转基因模型的环境毒理学

• 批准号: 6644139
• 负责人: GLEN K ANDREWS
• 金额: $ 34.4万
• 依托单位: UNIVERSITY OF KANSAS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 1991
• 资助国家: 美国
• 起止时间: 1991-08-05 至 2006-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6644139
• 关键词: cadmium; environmental toxicology; enzyme mechanism; gene expression; gene mutation; genetic manipulation; genetic mapping; genetic promoter element; genetic regulatory element; genetically modified animals; histopathology; immunocytochemistry; ion exchange chromatography; laboratory mouse; metal poisoning; metallothionein; microinjections; model design /development; northern blottings; nucleic acid hybridization; oxidative stress; polymerase chain reaction; protein biosynthesis; protein structure function; solution hybridization; toxicant screening; transcription factor; western blottings

DESCRIPTION (provided by applicant): The overall long-term objective of these studies is to apply molecular, biochemical and transgenic approaches to study environmental health-related issues. Current studies focus on the mechanisms by which the toxic metal Cd, and the essential metal Zn regulate gene expression. Cd is a widespread environmental toxin that poses an increasing threat to public health. It is a common industrial pollutant that is also present in cigarette smoke. Cd poisoning causes damage to many major organ systems, leading to Itai-Itai disease, retardation of growth, sterility and cancer. In contrast, Zn is an essential metal, which is required for the activity of hundreds of proteins, but is toxic when in high concentration. Specifically, our studies concentrate on metal-response element-binding transcription factor-1 (MTF-1), which coordinates the Cd- and Zn-induced transcription of several protective genes (e.g., the metal chelator metallothionein, the metal exporter zinc-transporter-1, and gamma-glutamylcysteine synthetase heavy chain, the rate limiting step in glutathione synthesis). MTF-1 functions as a cellular metal-sensor, but the molecular mechanisms by which it senses different metals are not well understood. Our studies suggest that Cd and Zn utilize overlapping yet distinct mechanisms for activation of gene expression using MTF-1. Remarkably, the mouse MTF-1 gene is essential and homozygous knockout embryos die at midgestation, thus underscoring the importance of this transcription factor. Whether MTF-1 is an essential gene in other species remains to be determined, as does the function of this protein during development. The six zinc-finger domain of this factor is highly conserved from insects to mammals, which indicates a conserved function. Therefore, the specific aims of this proposal are to: 1) Identify proteins which interact with MTF-1 specifically during Cd versus Zn induction, and examine their roles in MTF-1 -regulation of gene expression; 2) Determine the roles of histone acetylation in the MTF-1 activation of gene expression; and 3) Develop the Zebrafish as a model system to reveal essential functions of MTF-1 during embryonic development. Proteins which interact with MTF-1 will be studied using Superose-6 HPLC, immunoprecipitation, binding-site chromatography and mass spectrometry of proteolytic peptides. Roles of histone acetylation will be examined using chromatin immunoprecipitation, co-transfection with HAT expression vectors, detection of specific HAT proteins in the MTF-l complex, and analysis of MTF-l functions in yeast with mutations in HAT genes. Functions of MTF-l during development will be examined in Zebrafish using morpholino antisense oligonucleotides, whole mount in situ hybridization and morphometric analyses of developing embryos.

描述（由申请人提供）：这些研究的总体长期目标是应用分子，生化和转基因方法来研究与环境相关的问题。目前的研究主要集中在有毒金属Cd和必需金属Zn调控基因表达的机制上。Cd是一种广泛存在的环境毒素，对公众健康构成越来越大的威胁。它是一种常见的工业污染物，也存在于香烟烟雾中。镉中毒对许多主要器官系统造成损害，导致Itai-Itai病、生长迟缓、不育和癌症。相反，锌是一种必需的金属，它是数百种蛋白质活性所必需的，但高浓度时是有毒的。具体来说，我们的研究集中在金属反应元件结合转录因子-1 （MTF-1）上，它协调镉和锌诱导的几种保护基因的转录（例如，金属螯合物金属硫蛋白，金属出口锌转运蛋白-1和γ -谷氨酰半胱氨酸合成酶重链，谷胱甘肽合成的限速步骤）。MTF-1具有细胞金属传感器的功能，但其感知不同金属的分子机制尚不清楚。我们的研究表明，镉和锌利用重叠但不同的机制激活MTF-1基因表达。值得注意的是，小鼠MTF-1基因是必不可少的，纯合子敲除胚胎在妊娠中期死亡，从而强调了该转录因子的重要性。MTF-1在其他物种中是否也是一种必需基因还有待确定，这种蛋白在发育过程中的功能也有待确定。该因子的6锌指结构域从昆虫到哺乳动物都高度保守，表明其具有保守功能。因此，本研究的具体目标是：1)鉴定在Cd和Zn诱导过程中与MTF-1特异性相互作用的蛋白，并研究它们在MTF-1调控基因表达中的作用；2)确定组蛋白乙酰化在MTF-1激活基因表达中的作用；3)以斑马鱼为模型系统，揭示MTF-1在胚胎发育过程中的基本功能。与MTF-1相互作用的蛋白质将使用superse -6 HPLC，免疫沉淀，结合位点色谱和蛋白水解肽的质谱法进行研究。组蛋白乙酰化的作用将通过染色质免疫沉淀、HAT表达载体共转染、mtf - 1复合体中特定HAT蛋白的检测以及HAT基因突变酵母中mtf - 1功能的分析来检测。我们将利用形态学反义寡核苷酸、全载原位杂交和发育中胚胎的形态测定分析来研究mtf - 1在斑马鱼发育过程中的功能。