Zebrafish ES cell lines for targeted mutagenesis

描述（由申请人提供）：斑马鱼具有使其成为脊椎动物发育和人类疾病遗传研究的理想模型的特征。虽然大规模的正向诱变筛选已成功地应用于斑马鱼，以确定调控早期发育和人类疾病的基因，方法是不可用于通过插入诱变靶向基因失活。本研究的目的是利用斑马鱼胚胎干细胞（ES）和原始生殖细胞（PGC）系开发基因打靶方法。为了实现这一目标，现有的斑马鱼ES细胞培养系统将被优化用于生产敲除系的鱼。体外抗体筛选将用于鉴定在细胞经历基因靶向事件后仍有能力贡献宿主胚胎生殖系的ES细胞集落。此外，将建立对宿主生殖系有更有效贡献的PGC培养物，并评价生殖系传播。为了证明这种基因靶向方法的可行性，ES细胞系将用于靶向对正常发育和模式形成重要的基因的失活，产生具有明显和良好表征的表型的敲除鱼。本研究的具体目的是：1）鉴定特异性识别多能和生殖系感受态斑马鱼ES细胞集落的抗体。2)使用先前建立的方法分离具有ntl和hag基因破坏拷贝的ES细胞集落，并使用特定目的1中鉴定的抗体结合核型分析选择具有生殖系感受态和二倍体的那些集落。3)使用携带失活的ntl或hag基因的二倍体、生殖系感受态ES细胞培养物来产生敲除的鱼类品系。4)使用先前开发的方法建立后期胚胎的PGS培养物，并确定培养的PC是否比ES细胞更有效地产生生殖系嵌合体和活的F1胚胎。斑马鱼是胚胎发育和人类疾病遗传学研究的重要模型。从这项工作中开发的基于干细胞的基因靶向方法将补充目前应用于斑马鱼的其他遗传方法，并增加这种生物体作为研究人类发育和疾病中重要基因的模型的价值。

DESCRIPTION (provided by applicant): The zebrafish possesses characteristics that make it an ideal model for genetic studies of vertebrate development and human disease. Although large-scale forward mutagenesis screens have been successfully applied to the zebrafish to identify genes that regulate early development and human disease, methods are not available for targeted gene inactivation by insertional mutagenesis. The goal of this research is to develop gene targeting methods using zebrafish embryonic stem (ES) cell and primordial germ cell (PGC) lines. To accomplish this goal, the existing zebrafish ES cell culture system will be optimized for use in the production of knockout lines of fish. An in vitro antibody screen will be used to identify colonies of ES cells that remain competent to contribute to the germ line of a host embryo after the cells have undergone a gene targeting event. Also, PGC cultures that should contribute more efficiently to the host germ line will be established and evaluated for germ line transmission. To demonstrate the feasibility of this gene targeting approach, the ES cell lines will be utilized to target the inactivation of genes that are important for normal development and pattern formation, producing knockout fish possessing obvious and well-characterized phenotypes. The specific aims of this research are: 1) Identify antibodies that specifically recognize pluripotent and germ line competent zebrafish ES cell colonies. 2) Use previously established methods to isolate colonies of ES cells that possess disrupted copies of the ntl and hag genes and select those colonies that are germ line competent and diploid using the antibodies identified in specific aim 1 combined with karyotype analysis. 3) Use the diploid, germ line competent ES cell cultures that carry an inactivated ntl or hag gene to generate knockout lines of fish. 4) Use previously developed methods to establish cultures of PGSs from late-stage embryos and determine if the cultured PCs generate germ line chimeras and viable F1 embryos more efficiently than ES cells. The zebrafish is an important model for genetic studies of embryo development and human disease. The stem cell-based gene targeting approach developed from this work will complement other genetic methods currently applied to zebrafish and increase the value of this organism as a model for the study of genes important in human development and disease.