Microhomology-mediated end-joining Knock-In approaches to delete the allergenic domain of trout parvalbumin beta-1. Preliminary results in F0 animals and feedback.

Open research Europe Pub Date : 2025-02-25 eCollection Date: 2024-01-01 DOI:10.12688/openreseurope.18223.2
Veronique Lebret, Cecile Duret, Amaury Herpin, Pierre-Yves Rescan
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引用次数: 0

Abstract

Background: Gene editing techniques offer new opportunities to improve important traits in aquaculture. The allergenicity of fish flesh is a major problem in aquaculture. Parvalbumin (Parv) is the most prevalent fish allergen. For instance, in salmonids, a single parvalbumin beta-1 protein (parvb1) has been identified as an allergen in specific patients. Therefore, generating trout carrying two parvb1 alleles deleted from the allergenic peptide-encoding region could prevent allergies in these sensitive individuals.

Methods: Here, we describe the application of the Crispr/cas9 system in an attempt to delete parvb1 exon 2 encoding the allergenic peptide and, alternatively, to replace exon 2 of parvb1 with exon2 of parvalbumin beta-2 protein (parvb2,) which does not encode the allergenic peptide. Exon skipping and swapping were pursued through microhomology-mediated end-joining (MMEJ) knock-In using specifically designed double-stranded donor DNA.

Results: Genotyping of approximately 200 F0 fingerlings originating from eggs injected with donor DNA designed for exon 2 skipping led to the identification of only one animal carrying an allele lacking exon 2. Genotyping of approximately 150 fingerlings originating from eggs injected with donor DNA for exon 2 swapping did not result in any trout carrying the expected modified allele.

Conclusions: These preliminary results indicate the potential difficulties associated with the MMEJ KI experiments performed in farmed fish. Finally, new genomic techniques in aquaculture are further discussed in the context of lively debates taking place in the European parliament regarding a possible revision of the current law that determines the legal status of farm animals modified by genome editing. Gene editing, microhomology-mediated end-joining knock-in, parvalbumin, allergenicity, trout, and genetically modified organisms (GMOs).

微同源介导的末端连接敲入方法删除鳟鱼小白蛋白β -1的致敏结构域。F0动物的初步结果和反馈。
背景:基因编辑技术为改善水产养殖的重要性状提供了新的机会。鱼类的致敏性是水产养殖中的一个主要问题。细小白蛋白(Parv)是最常见的鱼类过敏原。例如,在鲑鱼中,一种单一的细小蛋白β -1蛋白(parvb1)已被确定为特定患者的过敏原。因此,产生携带两个parvb1等位基因的鳟鱼,从致敏肽编码区删除,可以防止这些敏感个体的过敏。方法:在这里,我们描述了Crispr/cas9系统的应用,试图删除parvb1编码致敏肽的外显子2,或者用不编码致敏肽的parvb1 β -2蛋白(parvb2)的外显子2替换parvb1的外显子2。外显子跳跃和交换是通过微同源介导的末端连接(MMEJ)敲入,使用专门设计的双链供体DNA。结果:对大约200只F0种鱼种进行基因分型,这些鱼种来源于注射了专为外显子2跳过而设计的供体DNA的卵,结果发现只有一只动物携带缺乏外显子2的等位基因。对大约150只来自注入供体DNA进行外显子2交换的卵的鱼种进行基因分型,没有发现任何鳟鱼携带预期的修饰等位基因。结论:这些初步结果表明,在养殖鱼类中进行MMEJ - KI实验可能存在困难。最后,在欧洲议会就现行法律的可能修订进行激烈辩论的背景下,进一步讨论了水产养殖中的新基因组技术,该法律确定了通过基因组编辑修改的农场动物的法律地位。基因编辑,微同源介导的末端连接敲入,小白蛋白,过敏原性,鳟鱼和转基因生物(GMOs)。
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