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胚胎背主动脉注射腺相关病毒 CRISPR/Cas9 载体一步法遗传修饰鸡。

One-Step Genetic Modification by Embryonic Doral Aorta Injection of Adenoviral CRISPR/Cas9 Vector in Chicken.

机构信息

Shanghai Key Laboratory of Veterinary Biotechnology, Department of Animal Science, School of Agriculture and Biology, Shanghai Jiaotong University, Shanghai 200240, China.

Animal Husbandry and Veterinary Research Institute, Shanghai Academy of Agricultural Science, Shanghai 200030, China.

出版信息

Int J Mol Sci. 2024 Aug 9;25(16):8692. doi: 10.3390/ijms25168692.

Abstract

In the avian species, genetic modification by cell nuclear transfer is infeasible due to its unique reproductive system. The in vitro primordial germ cell modification approach is difficult and cumbersome, although it is the main method of genetic modification in chickens. In the present study, the adenoviral CRISPR/Cas9 vector was directly microinjected into the dorsal aorta of chicken embryos to achieve in vivo genetic modification. The results demonstrated that (), a candidate gene crucial for feather development, was widely knocked out, and an 8bp deletion was the predominant mutation that occurred in multiple tissues in chimeras, particularly in the gonad (2.63-11.57%). As we expected, significant modification was detected in the sperm of G0 (0.16-4.85%), confirming the potential to generate homozygous chickens and establishing this vector as a simple and effective method for genetic modification in avian species.

摘要

在禽类物种中,由于其独特的生殖系统,通过细胞核转移进行基因修饰是不可行的。体外原始生殖细胞修饰方法虽然是鸡的主要基因修饰方法,但却很困难和繁琐。在本研究中,腺病毒 CRISPR/Cas9 载体被直接注射到鸡胚的背主动脉中,以实现体内基因修饰。结果表明,(),一个对羽毛发育至关重要的候选基因,被广泛敲除,并且在嵌合体的多个组织中,特别是在性腺(2.63-11.57%)中,主要发生 8bp 的缺失。正如我们所预期的,在 G0 精子中检测到明显的修饰(0.16-4.85%),证实了产生纯合鸡的潜力,并确立了该载体作为禽类物种中简单有效的基因修饰方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dadd/11354862/e73996fccee6/ijms-25-08692-g001.jpg

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