CrisprBuildr: an open-source application for CRISPR-mediated genome engineering in Drosophila melanogaster.

Nicole Horsley, Adam von Barnau Sythoff, Mark Delgado, Selina Liu, Clemens Cabernard
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Abstract

CRISPR/Cas9 is a powerful tool for targeted genome engineering experiments. With CRISPR/Cas9, genes can be deleted or modified by inserting small peptides, fluorescent proteins or other tags for protein labelling experiments. Such experiments are important for detailed protein characterization in vivo. However, designing and cloning the corresponding constructs can be repetitive, time consuming and laborious. To aid users in CRISPR/Cas9-based genome engineering experiments, we built CrisprBuildr, a web-based application that allows users to delete genes or insert fluorescent proteins at the N- or C-terminus of their gene of choice. The application is built on the Drosophila melanogaster genome but can be used as a template for other available genomes. We have also generated new tagging vectors, using EGFP and mCherry combined with the small peptide SspB-Q73R for use in iLID-based optogenetic experiments. CrisprBuildr guides users through the process of designing guide RNAs and repair template vectors. CrisprBuildr is an open-source application and future releases could incorporate additional tagging or deletion vectors, genomes or CRISPR applications.

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CrisprBuildr:在果蝇中进行crispr介导的基因组工程的开源应用程序。
CRISPR/Cas9是靶向基因组工程实验的有力工具。使用CRISPR/Cas9,可以通过插入小肽、荧光蛋白或其他标签来删除或修饰基因,进行蛋白质标记实验。这样的实验对于体内蛋白质的详细表征是重要的。然而,设计和克隆相应的构造可能是重复的、耗时的和费力的。为了帮助用户进行基于CRISPR/ cas9的基因组工程实验,我们构建了CrisprBuildr,这是一个基于网络的应用程序,允许用户在选择的基因的N端或c端删除基因或插入荧光蛋白。该应用程序是建立在果蝇基因组上的,但可以作为其他可用基因组的模板。我们还生成了新的标记载体,使用EGFP和mCherry结合小肽SspB-Q73R用于基于ilid的光遗传学实验。CrisprBuildr指导用户设计引导rna和修复模板载体的过程。CrisprBuildr是一个开源应用程序,未来的版本可能会包含额外的标记或删除载体、基因组或CRISPR应用程序。
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