Light up the embryos: knock-in reporter generation for mouse developmental biology

被引:3
|
作者
Gu, Bin [1 ,2 ,3 ]
机构
[1] Hosp Sick Children, Program Dev & Stem Cell Biol, Toronto, ON, Canada
[2] Michigan State Univ, Coll Human Med, Dept Obstet Gynecol & Reprod Biol, E Lansing, MI 48824 USA
[3] Michigan State Univ, Inst Quantitat Hlth Sci & Engn, E Lansing, MI 48824 USA
关键词
CRISPR-Cas9; genome editing; knock-in reporter; HDR; embryo; EFFICIENT GENERATION; GENOME; MICE; VIVO; TECHNOLOGY; EXPRESSION; ALLELES; CRISPR; CELLS;
D O I
10.1590/1984-3143-AR2020-0055
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Developmental biology seeks to understand the sophisticated regulated process through which a single cell - a fertilized egg - generates a highly organized organism. The most effective way to reveal the nature of these processes is to follow single cells and cell lineages in real-time. Recent advances in imaging equipment, fluorescent tags and computational tools have made long term multi-color imaging of cells and embryos possible. However, there is still one major challenging for achieving live imaging of mammalian embryos- the generation of embryos carrying reporters that recapitulate the endogenous expression pattern of marker genes. Recent developments of genome editing technology played important roles in enabling efficient generation of reporter mouse models. This mini review discusses recent developments of technologies for efficiently generate knock-in reporter mice and the application of these models in live imaging development. With these developments, we are starting to realize the long-sought promises of realtime analysis of mammalian development.
引用
收藏
页数:6
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