首页|基于小型化Cas蛋白的CRISPR/Gal4BD-Cas供体适配基因编辑系统研究

基于小型化Cas蛋白的CRISPR/Gal4BD-Cas供体适配基因编辑系统研究

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在哺乳动物细胞中,利用同源引导修复(homology-directed repair,HDR)机制的基因编辑策略能够实现精准的点编辑和敲入,但是HDR的低效性严重制约了该策略在精准医疗和分子设计育种中的应用。鉴于HDR机制所需的供体DNA模板不能自主募集到基因组双链断裂(double-stranded break,DSB)处,本课题组提出了供体适配系统(donor adapting system,DAS)的概念并开发出CRISPR/SpCas9-Gal4BD供体适配基因编辑系统。由于SpCas9蛋白分子较大,与Gal4BD适配器结合不利于表达、病毒载体包装及活体递送等过程,因此本研究进一步采用两种小型化Cas蛋白——路邓葡萄球菌(Staphylococcus lugdunensis)源SlugCas9变体SlugCas9-HF与 氨基酸球菌(Acidaminococcus sp。)源 AsCasl2a,开发了新型的 CRISPR/Gal4BD-SlugCas9 和CRISPR/Gal4BD-AsCas12a供体适配基因编辑系统。通过SSA活性报告实验初步证明了 Gal4BD与SlugCas9、AsCasl2aN-端融合对其打靶活性影响较小。通过HDR效率报告实验进行功能验证并优化供体设计方案,结果表明:对于 CRISPR/Gal4BD-AsCasl2a DAS,适配器结合序列(binding sequence,BS)与供体 5'-端融合(BS-dsDNA)效果较好;对于CRISPR/Gal4BD-SlugCas9 DAS,则 BS与供体3'-端融合(dsDNA-BS)较佳。最终,利用CRISPR/Gal4BD-SlugCas9 DAS 对 HEK293T 细胞中的 EMX1、NUDT5、AAVS1 三个基因位点分别实现了 24%、37%、31%的精准编辑,相比对照组得到了显著提高。本研究为供体适配基因编辑系统的进一步优化提供了参考和借鉴,为后续动物分子设计育种应用研究提供了新的基因编辑工具。
CRISPR/Gal4BD-Cas donor adapting systems based on miniaturized Cas proteins for improved gene editing
Targeted precise point editing and knock-in can be achieved by homology-directed repair(HDR)based gene editing strategies in mammalian cells.However,the inefficiency of HDR strategies seriously restricts their application in precision medicine and molecular design breeding.In view of the problem that exogenous donor DNA cannot be efficiently recruited autonomously at double-stranded breaks(DSBs)when using HDR strategies for gene editing,the concept of donor adapting system(DAS)was proposed and the CRISPR/Cas9-Gal4BD DAS was developed previously.Due to the large size of SpCas9 protein,its fusion with the Gal4BD adaptor is inconvenient for protein expression,virus vector packaging and in vivo delivery.In this study,two novel CRISPR/Gal4BD-SlugCas9 and CRISPR/Gal4BD-AsCasl2a DASs were further developed,using two miniaturized Cas proteins,namely SlugCas9-HF derived from Staphylococcus lugdunensis and AsCas12a derived from Acidaminococcus sp.Firstly,the SSA reporter assay was used to assess the targeting activity of different Cas-Ga14BD fusions,and the results showed that the fusion of Ga14BD with SlugCas9 and AsCasl2a N-terminals had minimal distraction on their activities.Secondly,the HDR efficiency reporter assay was conducted for the functional verification of the two DASs and the corresponding donor patterns were optimized simultaneously.The results demonstrated that the fusion of the Gal4BD adaptor binding sequence at the 5'-end of intent dsDNA template(BS-dsDNA)was better for the CRISPR/Gal4BD-AsCasl2a DAS.while for the CRISPR/Ga14BD-SlugCas9 DAS,the dsDNA-BS donor pattern was recommended.Finally,CRISPR/Gal4BD-SlugCas9 DAS was used to achieve gene editing efficiency of 24%,37%and 31%respectively for EMX1,NUDT5 and AAVSl gene loci in HEK293T cells,which was significantly increased compared with the controls.In conclusion,this study provides a reference for the subsequent optimization of the donor adapting systems,and expands the gene editing technical toolbox for the researches on animal molecular design breeding.

gene editinghomology-directed repairdonor adaptingminiaturized Cas proteinsadaptor

杨森、马宝霞、钱泓润、崔婕妤、张潇筠、李利达、魏泽辉、张智英、王建刚、徐坤

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西北农林科技大学动物科技学院,杨凌 712100

基因编辑 同源引导修复 供体适配 小型化Cas蛋白 适配器

农业农村部农业生物育种重大专项农业农村部农业生物育种重大专项

2023ZD040742023ZD04051

2024

遗传
中国遗传学会 中国科学院遗传与发育生物学研究所

遗传

CSTPCD北大核心
影响因子:1.082
ISSN:0253-9772
年,卷(期):2024.46(9)