Suppr超能文献

CRISPR/Cas9 核酸酶在文昌鱼基因组编辑中的应用。

Application of CRISPR/Cas9 Nuclease in Amphioxus Genome Editing.

机构信息

State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Xiamen University, Xiangan District, Xiamen 361102, Fujian, China.

出版信息

Genes (Basel). 2020 Nov 5;11(11):1311. doi: 10.3390/genes11111311.

Abstract

The cephalochordate amphioxus is a promising animal model for studying the origin of vertebrates due to its key phylogenetic position among chordates. Although transcription activator-like effector nucleases (TALENs) have been adopted in amphioxus genome editing, its labor-intensive construction of TALEN proteins limits its usage in many laboratories. Here we reported an application of the CRISPR/Cas9 system, a more amenable genome editing method, in this group of animals. Our data showed that while co-injection of mRNAs and sgRNAs into amphioxus unfertilized eggs caused no detectable mutations at targeted loci, injections of mRNAs and sgRNAs at the two-cell stage, or of Cas9 protein and sgRNAs before fertilization, can execute efficient disruptions of targeted genes. Among the nine tested sgRNAs (targeting five genes) co-injected with Cas9 protein, seven introduced mutations with efficiency ranging from 18.4% to 90% and four caused specific phenotypes in the injected embryos. We also demonstrated that monomerization of sgRNAs via thermal treatment or modifying the sgRNA structure could increase mutation efficacies. Our study will not only promote application of genome editing method in amphioxus research, but also provide valuable experiences for other organisms in which the CRISPR/Cas9 system has not been successfully applied.

摘要

文昌鱼是脊索动物中一个关键的进化分支,是研究脊椎动物起源的理想动物模型。尽管转录激活样效应物核酸酶(TALENs)已被用于文昌鱼基因组编辑,但 TALEN 蛋白的构建繁琐限制了其在许多实验室的应用。在这里,我们报道了 CRISPR/Cas9 系统(一种更易于使用的基因组编辑方法)在该动物群中的应用。我们的数据表明,尽管将 mRNAs 和 sgRNAs 共注射到文昌鱼未受精卵中不会在靶位引起可检测的突变,但在二细胞阶段注射 mRNAs 和 sgRNAs,或在受精前注射 Cas9 蛋白和 sgRNAs,可以有效地破坏靶基因。在与 Cas9 蛋白共注射的 9 个测试 sgRNAs(靶向 5 个基因)中,有 7 个 sgRNA 引起了 18.4%至 90%的突变效率,并在注射胚胎中引起了 4 种特定的表型。我们还证明,通过热处理或修饰 sgRNA 结构使 sgRNA 单体化可以提高突变效率。我们的研究不仅将促进基因组编辑方法在文昌鱼研究中的应用,也将为其他尚未成功应用 CRISPR/Cas9 系统的生物体提供宝贵的经验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e414/7694359/5f9c9cde79a2/genes-11-01311-g001.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