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靶向基因插入鸡原始生殖细胞的 Z 染色体用于开发禽类性别鉴定模型。

Targeted gene insertion into Z chromosome of chicken primordial germ cells for avian sexing model development.

机构信息

Department of Agricultural Biotechnology, Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul, South Korea.

出版信息

FASEB J. 2019 Jul;33(7):8519-8529. doi: 10.1096/fj.201802671R. Epub 2019 Apr 5.

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated protein 9 (Cas9) have facilitated the production of genome-edited animals for use as models. Because of their unique developmental system, avian species offer many advantages as model vertebrates. Here, we report the development of novel chicken models using the CRISPR/Cas9-mediated nonhomologous end joining repair pathway in chicken primordial germ cells (PGCs). Through the introduction of a donor plasmid containing short guide RNA recognition sequences and CRISPR/Cas9 plasmids into chicken PGCs, exogenous genes of donor plasmids were precisely inserted into target loci, and production of transgenic chickens was accomplished through subsequent transplantation of the Z chromosome-targeted PGCs. Using this method, we successfully accomplished the targeted gene insertion to the chicken sex Z chromosome without detected off-target effects. The genome-modified chickens robustly expressed green fluorescent protein from the Z chromosome, which could then be used for easy sex identification during embryogenesis. Our results suggest that this powerful genome-editing method could be used to develop many chicken models and should significantly expand the application of genome-modified avians.-Lee, H. J., Yoon, J. W., Jung, K. M., Kim, Y. M., Park, J. S., Lee, K. Y., Park, K. J., Hwang, Y. S., Park, Y. H., Rengaraj, D., Han, J. Y. Targeted gene insertion into Z chromosome of chicken primordial germ cells for avian sexing model development.

摘要

簇状规律间隔短回文重复序列(CRISPR)和 CRISPR 相关蛋白 9(Cas9)促进了基因组编辑动物的产生,可作为模型使用。由于其独特的发育系统,禽类作为模型脊椎动物具有许多优势。在这里,我们报告了使用 CRISPR/Cas9 介导的非同源末端连接修复途径在鸡原始生殖细胞(PGC)中开发新型鸡模型的情况。通过将含有短向导 RNA 识别序列和 CRISPR/Cas9 质粒的供体质粒引入鸡 PGC 中,供体质粒的外源基因被精确地插入靶位,并且通过随后移植靶向 Z 染色体的 PGC 来完成转基因鸡的产生。使用这种方法,我们成功地将靶向基因插入到鸡的性 Z 染色体中,而没有检测到脱靶效应。经过基因组修饰的鸡从 Z 染色体上强烈表达绿色荧光蛋白,这可用于胚胎发生期间进行简单的性别鉴定。我们的结果表明,这种强大的基因组编辑方法可用于开发许多鸡模型,并且应该显著扩展基因组修饰禽类的应用。-Lee,HJ,Yoon,JW,Jung,KM,Kim,YM,Park,JS,Lee,KY,Park,KJ,Hwang,YS,Park,YH,Rengaraj,D,Han,JY 靶向基因插入鸡原始生殖细胞的 Z 染色体用于开发禽类性别鉴定模型。

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