Salaudeen Asfar Lathif, Mateyko Nicholas, de Boer Carl G
Genome Science and Technology Graduate Program, University of British Columbia, Vancouver, BC, Canada.
School of Biomedical Engineering, University of British Columbia, Vancouver, BC, Canada.
bioRxiv. 2025 Apr 9:2025.04.09.648054. doi: 10.1101/2025.04.09.648054.
Guide RNA (gRNA) arrays can enable targeting multiple genomic loci simultaneously using CRISPR-Cas9. In this study, we present a streamlined and efficient method to rapidly construct gRNA arrays with up to 10 gRNA units in a single day. We demonstrate that gRNA arrays maintain robust functional activity across all positions, and can incorporate libraries of gRNAs, combining scalability and multiplexing. Our approach will streamline combinatorial perturbation research by enabling the economical and rapid construction, testing, and iteration of gRNA arrays.
引导RNA(gRNA)阵列能够利用CRISPR-Cas9同时靶向多个基因组位点。在本研究中,我们提出了一种简化且高效的方法,可在一天内快速构建多达10个gRNA单元的gRNA阵列。我们证明,gRNA阵列在所有位置均保持强大的功能活性,并且可以整合gRNA文库,兼具可扩展性和多重性。我们的方法将通过实现gRNA阵列的经济、快速构建、测试和迭代,简化组合扰动研究。