实验动物科学 ›› 2021, Vol. 38 ›› Issue (5): 75-.

• 研究进展 • 上一篇    

基于 CRISPR / Cas9 技术构建点突变小鼠概述

  

  1. ( 1. 北京实验动物研究中心有限公司,北京 102609)
    ( 2. 国家儿童医学中心 首都医科大学附属北京儿童医院 感染与病毒研究室,北京 100045)
  • 出版日期:2021-10-28 发布日期:2021-11-23

Overview of the Generation of Mice Carrying Point Mutation Based on CRISPR / Cas9 Technology

  1. ( 1. Beijing Laboratory Animal Research Center Co. ,Ltd. ,Beijing 102609, China)
    ( 2. National Center for Children’ s Health, Beijing Children’ s Hospital, Capital Medical University, Laboratory of Infection and Virology, Beijing 100045, China)
  • Online:2021-10-28 Published:2021-11-23

摘要:

摘要:2013 年 CRISPR( Clustered Regularly Interspaced Short Palindromic Repeats) / Cas( CRISPR-associated) 系统证实能够对人的细胞和其他真核细胞进行基因组编辑,现已广泛应用于生物医学领域。 本文对 CRISPR 在点突变小鼠构建中的应 用 进 行 概 述,为 单 向 导 RNA ( single guide RNA, sgRNA) 和 修 复 模 板 单 链 寡 聚 核 苷 酸 ( single-strand oligonucleotide,ssODN)的设计及体外转录、受精卵显微注射、子代鼠的鉴定等提供理论参考。

关键词: "> , CRISPR / Cas9, 基因组编辑, 点突变, 小鼠

Abstract:

Abstract: CRISPR ( Clustered Regularly Interspaced Short Palindromic Repeats ) / Cas ( CRISPR-associated ) system has been widely used in biomedicine since it was first demonstrated to be able to perform genome editing in human cells and other eukaryotic cells in 2013. In this paper, the applications of CRISPR / Cas9 in the generation of mice carrying point mutation will be reviewed, providing theoretical guidance for the design and in vitro transcription of single guide RNA ( sgRNA ) and single strand oligonucleotide ( ssODN ) , for microinjection of zygotes and for genotyping of founder and progeny mice.

Key words: CRISPR / Cas9, genome editing, point mutation, mice