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用睡美人转座子质粒和微型环对小鼠受精卵进行细胞质注射可高效产生种系转基因小鼠。

Cytoplasmic injection of murine zygotes with Sleeping Beauty transposon plasmids and minicircles results in the efficient generation of germline transgenic mice.

作者信息

Garrels Wiebke, Talluri Thirumala R, Ziegler Maren, Most Ilka, Forcato Diego O, Schmeer Marco, Schleef Martin, Ivics Zoltán, Kues Wilfried A

机构信息

Institut für Nutztiergenetik, Friedrich-Loeffler-Institut, Neustadt am Rübenberge, Germany.

Departamento de Biología Molecular, Universidad Nacional de Río Cuarto, Río Cuarto, Córdoba, Argentina.

出版信息

Biotechnol J. 2016 Jan;11(1):178-84. doi: 10.1002/biot.201500218. Epub 2015 Dec 4.

DOI:10.1002/biot.201500218
PMID:26470758
Abstract

Transgenesis in the mouse is an essential tool for the understanding of gene function and genome organization. Here, we describe a simplified microinjection protocol for efficient germline transgenesis and sustained transgene expression in the mouse model employing binary Sleeping Beauty transposon constructs of different topology. The protocol is based on co-injection of supercoiled plasmids or minicircles, encoding the Sleeping Beauty transposase and a transposon construct, into the cytoplasm of murine zygotes. Importantly, this simplified injection avoids the mechanical penetration of the vulnerable pronuclear membrane, resulting in higher survival rates of treated embryos and a more rapid pace of injections. Upon translation of the transposase, transposase-catalyzed transposition into the genome results in stable transgenic animals carrying monomeric transgenes. In summary, cytoplasmic injection of binary transposon constructs is a feasible, plasmid-based, and simplified microinjection method to generate genetically modified mice. The modular design of the components allows the multiplexing of different transposons, and the generation of multi-transposon transgenic mice in a single step.

摘要

小鼠转基因技术是理解基因功能和基因组组织的重要工具。在此,我们描述了一种简化的显微注射方案,用于在小鼠模型中通过使用不同拓扑结构的二元睡美人转座子构建体实现高效的种系转基因和持续的转基因表达。该方案基于将编码睡美人转座酶和转座子构建体的超螺旋质粒或微型环共同注射到小鼠受精卵的细胞质中。重要的是,这种简化的注射避免了对脆弱的原核膜的机械穿透,从而提高了处理后胚胎的存活率并加快了注射速度。转座酶翻译后,转座酶催化的转座进入基因组会产生携带单体转基因的稳定转基因动物。总之,二元转座子构建体的细胞质注射是一种可行的、基于质粒的简化显微注射方法,可用于生成基因修饰小鼠。各组件的模块化设计允许不同转座子的多重使用,并能在一步中生成多转座子转基因小鼠。

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