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从胚胎干细胞中在一代内生产基因敲入小鼠。

Production of knock-in mice in a single generation from embryonic stem cells.

机构信息

Laboratory for Synthetic Biology, RIKEN Quantitative Biology Center, Osaka, Japan.

Genetic Engineering Team, RIKEN Center for Life Science Technologies, Hyogo, Japan.

出版信息

Nat Protoc. 2017 Dec;12(12):2513-2530. doi: 10.1038/nprot.2017.110. Epub 2017 Nov 16.

Abstract

The system-level identification and analysis of molecular networks in mammals can be accelerated by 'next-generation' genetics, defined as genetics that does not require crossing of multiple generations of animals in order to achieve the desired genetic makeup. We have established a highly efficient procedure for producing knock-in (KI) mice within a single generation, by optimizing the genome-editing protocol for KI embryonic stem (ES) cells and the protocol for the generation of fully ES-cell-derived mice (ES mice). Using this protocol, the production of chimeric mice is eliminated, and, therefore, there is no requirement for the crossing of chimeric mice to produce mice that carry the KI gene in all cells of the body. Our procedure thus shortens the time required to produce KI ES mice from about a year to ∼3 months. Various kinds of KI ES mice can be produced with a minimized amount of work, facilitating the elucidation of organism-level phenomena using a systems biology approach. In this report, we describe the basic technologies and protocols for this procedure, and discuss the current challenges for next-generation mammalian genetics in organism-level systems biology studies.

摘要

哺乳动物的分子网络的系统级鉴定和分析可以通过“下一代”遗传学加速,下一代遗传学定义为不需要对动物进行多代杂交就可以实现所需遗传组成的遗传学。我们通过优化用于基因敲入 (KI) 胚胎干细胞的基因组编辑方案和用于生成完全由胚胎干细胞衍生的小鼠 (ES 小鼠) 的方案,在单个世代内建立了高效的 KI 小鼠生产程序。使用该方案,可以消除嵌合小鼠的产生,因此,不需要通过杂交嵌合小鼠来生产在体内所有细胞中携带 KI 基因的小鼠。我们的方案将产生 KI ES 小鼠所需的时间从大约一年缩短到约 3 个月。可以以最小的工作量生产各种 KI ES 小鼠,从而促进使用系统生物学方法阐明机体水平的现象。在本报告中,我们描述了该方案的基本技术和方案,并讨论了在机体水平系统生物学研究中进行下一代哺乳动物遗传学的当前挑战。

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