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通过CRISPR/Cas9系统建立的用于鸡性别分化的可诱导CYP19A1基因敲除模型()

An Inducible CYP19A1 Excision Model for Sexual Differentiation in Chicken () via the CRISPR/Cas9 System.

作者信息

Liu Guangzheng, Peng Yixiu, Li Zeyu, Zhu Xilin, Sun Hongyan, Chen Guohong, Zuo Qisheng, Niu Yingjie, Song Jiuzhou, Han Wei, Wei Wanhong, Li Bichun, Jin Kai

机构信息

Joint International Research Laboratory of Agriculture and Agri-Product Safety, Ministry of Education of China, Yangzhou University, Yangzhou 225009, China.

Key Laboratory of Animal Breeding Reproduction and Molecular Design for Jiangsu Province, College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.

出版信息

Vet Sci. 2025 Mar 22;12(4):296. doi: 10.3390/vetsci12040296.

Abstract

Aromatase, a crucial enzyme for estrogen synthesis, plays a vital role in gender determination and differentiation. This study aimed to establish an inducible knockout model of the chicken gene, which encodes aromatase, to support gender control in chickens. We selected the most efficient sgRNA target site and constructed an inducible knockout model based on the Tet-on system. The knockout efficiency reached 80% with 20 μg/mL DOX induction in vitro. The encapsulation of the plasmid with PEI and injection into eggs achieved a knockout efficiency of 45% in ovo. qRT-PCR analysis revealed a significant downregulation of female-related genes (, , ) and upregulation of male-related genes (, , ) in female chicken embryos after induction. Western blotting showed decreased protein expression of CYP19A1 and FOXL2, and increased SOX9 expression in female embryos post-DOX induction. Elisa detection further confirmed lower estradiol levels in the gonads of induced female embryos compared to normal and non-induced females. These findings demonstrate the successful establishment of an inducible knockout system for the gene in chickens, providing theoretical and technical support for the creation of new breeding materials for gender control.

摘要

芳香化酶是雌激素合成的关键酶,在性别决定和分化中起着至关重要的作用。本研究旨在建立鸡芳香化酶编码基因的诱导敲除模型,以支持鸡的性别控制。我们选择了最有效的sgRNA靶位点,并基于Tet-on系统构建了诱导敲除模型。在体外20μg/mL强力霉素诱导下,敲除效率达到80%。用聚乙烯亚胺包封质粒并注射到鸡蛋中,在体内的敲除效率达到45%。qRT-PCR分析显示,诱导后雌性鸡胚中与雌性相关的基因(、、)显著下调,与雄性相关的基因(、、)上调。蛋白质免疫印迹显示,强力霉素诱导后雌性胚胎中CYP19A1和FOXL2的蛋白表达降低,SOX9表达增加。酶联免疫吸附测定进一步证实,与正常和未诱导的雌性相比,诱导的雌性胚胎性腺中的雌二醇水平较低。这些发现表明成功建立了鸡基因的诱导敲除系统,为创造性别控制新育种材料提供了理论和技术支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b0b/12031565/c7784982535c/vetsci-12-00296-g001.jpg

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