Development of gene targeting in C. elegans and D. rerio using zinc finger

使用锌指开发秀丽隐杆线虫和斑马鱼基因打靶

• 批准号: 7085142
• 负责人: Matthew H Porteus
• 金额: $ 17.55万
• 依托单位: UT SOUTHWESTERN MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-06-01 至 2008-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7085142
• 关键词: Caenorhabditis elegans; gene mutation; gene targeting; genes; genome; human; neoplasm /cancer; nuclease; protein structure; zebrafish

DESCRIPTION (provided by applicant): The goal of this research is to develop methods for the precise modification of specific target genes in two important genetic model organisms, the nematode Caenorhabditis elegans and the zebrafish Danio rerio. Both nematodes and fish are powerful experimental systems that combine elegant developmental biology with large scale genetics. Both systems have contributed to our understanding of fundamental problems in cancer biology, including programmed cell death, the control of organogenesis, the interaction of cancer susceptibility genes with the environment, and the genetics of melanoma. An important limitation of these model systems is that techniques for site-specific manipulation of the genome are not currently available in either nematodes or fish. Thus, in contrast to murine embryonic stem cells and the yeast S. cerevisiae, it is not possible to knock out specific genes or to precisely control the time and place of gene expression. In the last two years, a powerful new approach to gene-targeting has been developed and successfully used in flies and in mammalian somatic cells. This technique uses chimeric zinc finger nucleases to stimulate precise targeting of specific genes in their native genomic context. The aim of this proposal is to induce targeted, heritable genetic changes via zinc finger nuclease-mediated homologous recombination in C. elegans and D. rerio. Initially we will employ a well-characterized zinc finger nuclease that recognizes the green fluorescent protein (GFP) gene. We will introduce the nuclease into transgenic nematodes and zebrafish that express GFP. We expect the resulting double-strand DNA breaks to stimulate mutagenic non-homologous end joining (NHEJ), leading to the loss of GFP signal. In the second phase, we will simultaneously introduce the nuclease and a repair template that will allow us to create precise mutations in the target locus by homologous recombination. Based on the success of this work we will then target native genes in the worm and the fish by designing novel nucleases and testing them in vitro and in vivo for activity against the targeted gene. We expect that, if successful, this novel approach would be a practical, flexible, and powerful technique that would find wide application, significantly increasing the power of these systems to illuminate human cancer biology.

描述（由申请人提供）：本研究的目的是开发用于精确修饰两种重要遗传模式生物（线虫秀丽隐杆线虫和斑马鱼）中特定靶基因的方法。线虫和鱼类都是强大的实验系统，它们将联合收割机优雅的发育生物学与大规模遗传学相结合。这两个系统都有助于我们理解癌症生物学中的基本问题，包括程序性细胞死亡，器官发生的控制，癌症易感基因与环境的相互作用，以及黑色素瘤的遗传学。这些模型系统的一个重要限制是，基因组的位点特异性操作技术目前在线虫或鱼类中不可用。因此，与小鼠胚胎干细胞和酵母S.在酿酒酵母中，不可能敲除特定基因或精确控制基因表达的时间和地点。在过去的两年中，一种强大的新的基因靶向方法已经开发出来，并成功地用于苍蝇和哺乳动物体细胞。该技术使用嵌合锌指核酸酶来刺激特异性基因在其天然基因组环境中的精确靶向。本研究的目的是通过锌指核酸酶介导的同源重组在C. elegans和D.雷里奥。最初，我们将采用一个良好的特点，锌指核酸酶，识别的绿色荧光蛋白（GFP）基因。我们将把核酸酶引入表达GFP的转基因线虫和斑马鱼中。我们预期所产生的双链DNA断裂会刺激致突变的非同源末端连接（NHEJ），导致GFP信号的丢失。在第二阶段，我们将同时引入核酸酶和修复模板，这将使我们能够通过同源重组在靶基因座中产生精确的突变。基于这项工作的成功，我们将通过设计新的核酸酶并在体外和体内测试它们对靶基因的活性来靶向蠕虫和鱼类中的天然基因。我们预计，如果成功，这种新方法将是一种实用，灵活和强大的技术，将得到广泛的应用，显着增加这些系统的能力，以阐明人类癌症生物学。