Sato Masahiro, Ohtsuka Masato, Watanabe Satoshi, Gurumurthy Channabasavaiah B
Section of Gene Expression Regulation, Frontier Science Research Center, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima, Kagoshima, 890-8544, Japan.
Division of Basic Molecular Science and Molecular Medicine, School of Medicine, Tokai University, Kanagawa, 259 1193, Japan.
Biol Direct. 2016 Mar 31;11(1):16. doi: 10.1186/s13062-016-0115-8.
In the recent years, sequence-specific nucleases such as ZFNs, TALENs, and CRISPR/Cas9 have revolutionzed the fields of animal genome editing and transgenesis. However, these new techniques require microinjection to deliver nucleic acids into embryos to generate gene-modified animals. Microinjection is a delicate procedure that requires sophisticated equipment and highly trained and experienced technicians. Though over a dozen alternate approaches for nucleic acid delivery into embryos were attempted during the pre-CRISPR era, none of them became routinely used as microinjection. The addition of CRISPR/Cas9 to the genome editing toolbox has propelled the search for novel delivery approaches that can obviate the need for microinjection. Indeed, some groups have recently developed electroporation-based methods that have the potential to radically change animal transgenesis. This review provides an overview of the old and new delivery methods, and discusses various strategies that were attempted during the last three decades. In addition, several of the methods are re-evaluated with respect to their suitability to deliver genome editing components, particularly CRISPR/Cas9, to embryos.
近年来,诸如锌指核酸酶(ZFNs)、转录激活样效应因子核酸酶(TALENs)和规律成簇间隔短回文重复序列/CRISPR相关蛋白9(CRISPR/Cas9)等序列特异性核酸酶已经彻底改变了动物基因组编辑和转基因领域。然而,这些新技术需要通过显微注射将核酸导入胚胎以产生基因修饰动物。显微注射是一个精细的过程,需要精密的设备以及训练有素且经验丰富的技术人员。尽管在CRISPR时代之前尝试了十几种将核酸导入胚胎的替代方法,但它们都没有像显微注射那样成为常规使用的方法。CRISPR/Cas9加入基因组编辑工具箱推动了对可避免显微注射需求的新型递送方法的探索。事实上,一些研究小组最近开发了基于电穿孔的方法,这些方法有可能从根本上改变动物转基因技术。本综述概述了新旧递送方法,并讨论了过去三十年中尝试的各种策略。此外,还对其中几种方法在向胚胎递送基因组编辑组件(特别是CRISPR/Cas9)方面的适用性进行了重新评估。