Liu Zi-Ling, Zhou Yu-Yu, Xu Qiu-Xuan, Wang Xing-Ce, Liu Tong-Xian, Tian Hong-Gang
Key Laboratory of Plant Protection Resources and Pest Management of Ministry of Education, Key Laboratory of Integrated Pest Management on the Loess Plateau of Ministry of Agriculture and Rural Affairs, College of Plant Protection, Northwest A&F University, Yangling, Shaanxi, China.
Institute of Entomology, Guizhou University, Guiyang, Guizhou, China.
Insect Sci. 2024 Sep 20. doi: 10.1111/1744-7917.13447.
The clustered regularly interspaced small palindromic repeats (CRISPR) / CRISPR-associated nuclease 9 (Cas9)-mediated gene editing technology has revolutionized the study of fundamental biological questions in various insects. Diverse approaches have been developed to deliver the single-guide RNA (sgRNA) and Cas9 to the nucleus of insect embryos or oocytes to achieve gene editing, including the predominant embryonic injection methods and alternative protocols through parental ovary delivery. However, a systematic comparative study of these approaches is limited, especially within a given insect. Here, we focused on revealing the detailed differences in CRISPR/Cas9-mediated gene editing between the embryo and ovary delivery methods in the beetle Tribolium castaneum, using the cardinal and tyrosine hydroxylase (TH) as reporter genes. We demonstrated that both genes could be efficiently edited by delivering Cas9/sgRNA ribonucleoproteins to the embryos by microinjection, leading to the mutant phenotypes and indels in the target gene sites. Next, the Cas9/sgRNA complex, coupled with a nanocarrier called Branched Amphiphilic Peptide Capsules (BAPC), were delivered to the ovaries of parental females to examine the efficacy of BAPC-mediated gene editing. Although we observed that a small number of beetles' progeny targeting the cardinal exhibited the expected white-eye phenotype, unexpectedly, no target DNA indels were found following subsequent sequencing analysis. In addition, we adopted a novel approach termed "direct parental" CRISPR (DIPA-CRISPR). However, we still failed to find gene-editing events in the cardinal or TH gene-targeted insects. Our results indicate that the conventional embryonic injection of CRISPR is an effective method to initiate genome editing in T. castaneum. However, it is inefficient by the parental ovary delivery approach.
成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关核酸酶9(Cas9)介导的基因编辑技术彻底改变了对各种昆虫基本生物学问题的研究。人们已经开发出多种方法将单向导RNA(sgRNA)和Cas9递送至昆虫胚胎或卵母细胞的细胞核以实现基因编辑,包括主要的胚胎注射方法以及通过亲代卵巢递送的替代方案。然而,对这些方法的系统比较研究有限,尤其是在特定昆虫中。在此,我们以朱砂眼基因和酪氨酸羟化酶(TH)作为报告基因,着重揭示在赤拟谷盗中胚胎递送方法与卵巢递送方法在CRISPR/Cas9介导的基因编辑方面的详细差异。我们证明,通过显微注射将Cas9/sgRNA核糖核蛋白递送至胚胎能够有效编辑这两个基因,从而导致靶基因位点出现突变表型和插入缺失。接下来,将Cas9/sgRNA复合物与一种名为分支两亲肽胶囊(BAPC)的纳米载体相结合,递送至亲代雌性的卵巢,以检验BAPC介导的基因编辑效果。尽管我们观察到少数靶向朱砂眼基因的甲虫后代表现出预期的白眼表型,但意外的是,后续测序分析未发现靶DNA插入缺失。此外,我们采用了一种名为“直接亲代”CRISPR(DIPA-CRISPR)的新方法。然而,我们仍然未能在靶向朱砂眼基因或TH基因的昆虫中发现基因编辑事件。我们的结果表明,传统的CRISPR胚胎注射法是在赤拟谷盗中启动基因组编辑的有效方法。然而,通过亲代卵巢递送方法效率较低。