Suppr超能文献

成熟过程中电穿孔时间对使用CRISPR/Cas9系统进行猪胚胎三基因编辑的影响。

Effects of the timing of electroporation during maturation on triple gene editing in porcine embryos using CRISPR/Cas9 system.

作者信息

Namula Zhao, Wittayarat Manita, Do Lanh Thi Kim, Van Nguyen Thanh, Lin Qingyi, Takebayashi Koki, Hirata Maki, Tanihara Fuminori, Otoi Takeshige

机构信息

College of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang 524088, China.

Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, 7708501, Japan.

出版信息

Vet Anim Sci. 2022 Feb 28;16:100241. doi: 10.1016/j.vas.2022.100241. eCollection 2022 Jun.

Abstract

Mosaicism, including alleles comprising both wild-type and mutant, is a serious problem for gene modification by gene editing using electroporation. One-step generation of F0 pigs with completely desired gene modifications saves cost and time, but the major obstacles have been mosaic mutations. We hypothesized that the timing of electroporation prior to fertilization (IVF) can increase the rates of biallelic mutation for multiple gene knockout as the permeability of mature oocytes is greater than that of zygotes. Hence, we determined whether the timing of electroporation during maturation (IVM) culture enhances triple gene editing in the resulting blastocysts. Three gRNAs targeting , and were simultaneously introduced into the oocytes that had been incubated for 40, 42, and 44 h from the start of the IVM culture. Electroporation with three gRNAs at 40 h and 42 h during IVM culture decreased the blastocyst formation rates and did not improve the mutation rates and target number of biallelic mutations in the resulting blastocysts. The blastocyst formation rate, mutation rates, and target numbers in the resulting blastocysts from oocytes treated by electroporation at 44 h of IVM culture were similar to those of control zygotes electroporated at 13 h after the initiation of IVF. In conclusion, multiple gene editing efficiency in the resulting blastocysts was comparable between oocytes electroporated before and after the fertilization, indicating that oocytes with completed maturation time may allow better functioning of materials accepting gene editing application.

摘要

镶嵌现象,包括同时含有野生型和突变型等位基因的情况,对于使用电穿孔进行基因编辑的基因修饰来说是一个严重问题。一步生成具有完全理想基因修饰的F0猪可节省成本和时间,但主要障碍一直是镶嵌突变。我们推测,由于成熟卵母细胞的通透性大于受精卵,在受精(体外受精)前进行电穿孔的时间可以提高多基因敲除的双等位基因突变率。因此,我们确定了在成熟(体外成熟)培养过程中进行电穿孔的时间是否能提高所得囊胚中的三基因编辑效率。将靶向、和的三种引导RNA同时导入从体外成熟培养开始已孵育40、42和44小时的卵母细胞中。在体外成熟培养的40小时和42小时用三种引导RNA进行电穿孔降低了囊胚形成率,并且没有提高所得囊胚中的突变率和双等位基因突变的靶点数量。在体外成熟培养44小时进行电穿孔处理的卵母细胞所得囊胚的囊胚形成率、突变率和靶点数量与体外受精开始后13小时进行电穿孔的对照受精卵相似。总之,所得囊胚中的多基因编辑效率在受精前后进行电穿孔的卵母细胞之间相当,这表明具有完整成熟时间的卵母细胞可能使接受基因编辑应用的物质发挥更好的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/8899406/31c5db220f1d/gr1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验