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用于培育和维持珍贵动物品系的生殖技术。

Reproductive technologies for the generation and maintenance of valuable animal strains.

作者信息

Kaneko Takehito

机构信息

Division of Science and Engineering, Graduate School of Arts and Science, Iwate University, Iwate 020-8551, Japan.

Department of Chemistry and Biological Sciences, Faculty of Science and Engineering, Iwate University, Iwate 020-8551, Japan.

出版信息

J Reprod Dev. 2018 Jun 22;64(3):209-215. doi: 10.1262/jrd.2018-035. Epub 2018 Apr 14.

Abstract

Many types of mutant and genetically engineered strains have been produced in various animal species. Their numbers have dramatically increased in recent years, with new strains being rapidly produced using genome editing techniques. In the rat, it has been difficult to produce knockout and knock-in strains because the establishment of stem cells has been insufficient. However, a large number of knockout and knock-in strains can currently be produced using genome editing techniques, including zinc-finger nuclease (ZFN), transcription activator-like effector nuclease (TALEN), and the clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated protein 9 (Cas9) system. Microinjection technique has also contributed widely to the production of various kinds of genome edited animal strains. A novel electroporation method, the "Technique for Animal Knockout system by Electroporation (TAKE)" method, is a simple and highly efficient tool that has accelerated the production of new strains. Gamete preservation is extremely useful for maintaining large numbers of these valuable strains as genetic resources in the long term. These reproductive technologies, including microinjection, TAKE method, and gamete preservation, strongly support biomedical research and the bio-resource banking of animal models. In this review, we introduce the latest reproductive technologies used for the production of genetically engineered animals, especially rats, using genome editing techniques and the efficient maintenance of valuable strains as genetic resources. These technologies can also be applied to other laboratory animals, including mice, and domestic and wild animal species.

摘要

在各种动物物种中已经产生了许多类型的突变体和基因工程菌株。近年来,它们的数量急剧增加,利用基因组编辑技术能够快速产生新的菌株。在大鼠中,由于干细胞的建立不足,很难产生基因敲除和基因敲入菌株。然而,目前使用包括锌指核酸酶(ZFN)、转录激活样效应核酸酶(TALEN)以及成簇规律间隔短回文重复序列(CRISPR)和CRISPR相关蛋白9(Cas9)系统在内的基因组编辑技术,可以产生大量的基因敲除和基因敲入菌株。显微注射技术也在各种基因组编辑动物菌株的产生中发挥了广泛作用。一种新的电穿孔方法,即“电穿孔动物基因敲除系统技术(TAKE)”方法,是一种简单且高效的工具,加速了新菌株的产生。配子保存对于长期维持大量这些珍贵菌株作为遗传资源极为有用。这些生殖技术,包括显微注射、TAKE方法和配子保存,有力地支持了生物医学研究以及动物模型的生物资源库建设。在本综述中,我们介绍了利用基因组编辑技术生产基因工程动物,特别是大鼠,以及作为遗传资源高效保存珍贵菌株所使用的最新生殖技术。这些技术也可应用于其他实验动物,包括小鼠,以及家养和野生动物物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb18/6021608/db4bcfbccebb/jrd-64-209-g001.jpg

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