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Generation of beta-lactoglobulin knock-out goats using CRISPR/Cas9

机译:使用CRISPR / Cas9生成β-乳球蛋白基因敲除山羊

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摘要

Goat’s milk, considered a substitute for cow’s milk, has a high nutritional value. However, goat’s milk contains various allergens, predominantly β-lactoglobulin (BLG). In this study, we employed the CRISPR/Cas9 system to target the BLG locus in goat fibroblasts for sgRNA optimization and generate BLG knock-out goats through co-injection of Cas9 mRNA and small guide RNAs (sgRNAs) into goat embryos at the one-cell stage. We firstly tested sgRNA editing efficiencies in goat fibroblast cells, and approximately 8.00%–9.09% of the cells were modified in single sgRNA-guided targeting experiment. Among the kids, the genome-targeting efficiencies of single sgRNA were 12.5% (10 ng/μL sg1) and 0% (10 ng/μL sg2) and efficiencies of dual sgRNAs were 25.0% (25 ng/μL sg2+sg3 group) and 28.6% (50 ng/μL sg2+sg3 group). Relative expression of BLG in BLG knock-out goat mammary glands significantly (p < 0.01) decreased as well as other milk protein coding genes, such as CSN1S1, CSN1S2, CSN2, CSN3 and LALBA (p < 0.05). As expected, BLG protein had been abolished in the milk of the BLG knock-out goat. In addition, most of the targeted kids were chimeric (3/4), and their various body tissues were edited simultaneously. Our study thus provides a basis for optimizing the quality of goat milk, which can be applied to biomedical and agricultural research.
机译:山羊奶被认为是牛奶的替代品,具有很高的营养价值。但是,山羊奶中含有多种过敏原,主要是β-乳球蛋白(BLG)。在这项研究中,我们采用CRISPR / Cas9系统靶向山羊成纤维细胞中的BLG基因座,以优化sgRNA,并通过将Cas9 mRNA和小指导RNA(sgRNA)共同注射到山羊胚胎中,从而将BLG基因敲除的山羊细胞阶段。我们首先在山羊成纤维细胞中测试了sgRNA编辑效率,并且在单个sgRNA引导的靶向实验中修饰了约8.00%–9.09%的细胞。在孩子中,单个sgRNA的基因组靶向效率分别为12.5%(10 ng /μLsg1)和0%(10 ng /μLsg2),双重sgRNA的效率为25.0%(25 ng /μLsg2 + sg3组)和28.6%(50 ng /μLsg2 + sg3组)。 BLG基因敲除山羊乳腺中BLG的相对表达以及其他乳蛋白编码基因(如CSN1S1,CSN1S2,CSN2,CSN3和LALBA)均显着降低(p <0.01)(p <0.05)。不出所料,BLG基因敲除山羊的乳汁中已消除了BLG蛋白。此外,大多数目标儿童都是嵌合体(3/4),并且可以同时编辑他们的各种身体组织。因此,我们的研究为优化羊奶质量提供了基础,可将其应用于生物医学和农业研究。

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