Microbiology Program, University of California Riverside, Riverside, CA, 92521, USA.
Department of Biology, University of California Riverside, Riverside, CA, 92521, USA.
Sci Rep. 2021 Dec 8;11(1):23625. doi: 10.1038/s41598-021-03130-0.
A difficult genome editing goal is the site-specific insertion of large genetic constructs. Here we describe the GENEWRITE system, where site-specific targetable activity of Cas endonucleases is coupled with the reverse transcriptase activity of the ORF2p protein of the human retrotransposon LINE-1. This is accomplished by providing two RNAs: a guide RNA targeting Cas endonuclease activity and an appropriately designed payload RNA encoding the desired insertion. Using E. coli as a simple platform for development and deployment, we show that with proper payload design and co-expression of helper proteins, GENEWRITE can enable insertion of large genetic payloads to precise locations, although with off-target effects, using the described approach. Based upon these results, we describe a potential strategy for implementation of GENEWRITE in more complex systems.
一个具有挑战性的基因组编辑目标是在特定位置插入大型基因构建体。在这里,我们描述了 GENEWRITE 系统,其中 Cas 内切酶的特异性靶向活性与人类反转录转座子 LINE-1 的 ORF2p 蛋白的逆转录酶活性偶联。这是通过提供两种 RNA 来实现的:一种靶向 Cas 内切酶活性的向导 RNA 和一种编码所需插入的适当设计的有效载荷 RNA。通过将大肠杆菌用作开发和部署的简单平台,我们表明,通过适当的有效载荷设计和辅助蛋白的共表达,GENEWRITE 可以在精确位置插入大型基因有效载荷,尽管使用描述的方法存在脱靶效应。基于这些结果,我们描述了在更复杂系统中实施 GENEWRITE 的潜在策略。