Kojin Bianca B, Tsujimoto Hitoshi, Jakes Emma, O'Leary Sarah, Adelman Zach N
Department of Entomology and Agrilife Research, Texas A&M University.
Department of Entomology and Agrilife Research, Texas A&M University;
J Vis Exp. 2021 Sep 10(175). doi: 10.3791/63008.
Mosquito gene editing has become routine in several laboratories with the establishment of systems such as transcription-activator-like effector nucleases (TALENs), zinc-finger nucleases (ZFNs), and homing endonucleases (HEs). More recently, clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) technology has offered an easier and cheaper alternative for precision genome engineering. Following nuclease action, DNA repair pathways will fix the broken DNA ends, often introducing indels. These out-of-frame mutations are then used for understanding gene function in the target organisms. A drawback, however, is that mutant individuals carry no dominant marker, making identification and tracking of mutant alleles challenging, especially at scales needed for many experiments. High-resolution melt analysis (HRMA) is a simple method to identify variations in nucleic acid sequences and utilizes PCR melting curves to detect such variations. This post-PCR analysis method uses fluorescent double-stranded DNA-binding dyes with instrumentation that has temperature ramp control data capture capability and is easily scaled to 96-well plate formats. Described here is a simple workflow using HRMA for the rapid detection of CRISPR/Cas9-induced indels and the establishment of mutant lines in the mosquito Ae. aegypti. Critically, all steps can be performed with a small amount of leg tissue and do not require sacrificing the organism, allowing genetic crosses or phenotyping assays to be performed after genotyping.
随着转录激活样效应核酸酶(TALENs)、锌指核酸酶(ZFNs)和归巢核酸内切酶(HEs)等系统的建立,蚊子基因编辑在多个实验室已成为常规操作。最近,成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白9(Cas9)技术为精确基因组工程提供了一种更简便、更廉价的替代方法。核酸酶作用后,DNA修复途径会修复断裂的DNA末端,常常引入插入缺失。然后利用这些移码突变来了解目标生物中的基因功能。然而,一个缺点是突变个体没有显性标记,这使得突变等位基因的鉴定和追踪具有挑战性,尤其是在许多实验所需的规模下。高分辨率熔解分析(HRMA)是一种识别核酸序列变异的简单方法,它利用PCR熔解曲线来检测此类变异。这种PCR后分析方法使用荧光双链DNA结合染料,其仪器具有温度梯度控制和数据捕获能力,并且很容易扩展到96孔板形式。本文描述了一种使用HRMA快速检测CRISPR/Cas9诱导的插入缺失并在埃及伊蚊中建立突变系的简单工作流程。至关重要的是,所有步骤都可以用少量腿部组织进行,并且不需要牺牲生物体,从而允许在基因分型后进行遗传杂交或表型分析。