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Discriminated sgRNAs-Based SurroGate System Greatly Enhances the Screening Efficiency of Plant Base-Edited Cells

查看全文 作  者:Wen [1]Xu;Yongxing [1]Yang;Ya [1]Liu;Guiting [1]Kang;Feipeng [1]Wang;Lu [1]Li;Xinxin [1]Lv;Si [1]Zhao;Shuang [1]Yuan;Jinling [1]Song;Ying [1]Wu;Feng [1]Feng;Xiaoqing [1]He;Chengwei [1]Zhang;Wei [1]Song;Jiuran [1]Zhao;Jinxiao [1]Yang 高影响力作者 机构地区:[1]Beijing Key Laboratory of Maize DNA Fingerprinting and Molecular Breeding,Beijing Academy of Agriculture&Forestry Sciences,Beijing 100080,China高影响力机构 出  处:《Molecular Plant》索引2020年第13卷第1期,共12页高影响力期刊 基  金:This work was supported by Beijing Academy of Agriculture&Forestry Scien ces,Beijing,China;The funding in eluded Innovative Team Con-struction Project of BAAFS(JNKYT201603);the Beijing Scholars Program(BSP041). 摘  要:The development of CRISPR/Cas9-mediated base editing has made genomic modification more efficient. However, selection of genetically modified cells from millions of treated cells, especially plant cells, is still challenging. In this study, an efficient surrogate reporter system based on a defective hygromycin resistance gene was established in rice to enrich base-edited cells. After step-by-step optimization, the Discriminated sgRNAs-based SurroGate system (DisSUGs) was established by artificially differentiating the editing abilities of a wild-type single guide RNA (sgRNA) targeting the surrogate reporter gene and an enhanced sgRNA targeting endogenous sites. The DisSUGs enhanced the efficiency of screening base-edited cells by 3- to 5-fold for a PmCDA1-based cytosine-to-tyrosine base editor (PCBE), and 2.5- to 6.5-fold for an adenine base editor (ABE) at endogenous targets. These targets showed editing efficiencies of <25% in the conventional systems. The DisSUGs greatly enhanced the frequency of homozygous substitutions and expanded the activity window slightly for both a PCBE and an ABE. Analyses of the total number of single-nucleotide variants from whole-genome sequencing revealed that, compared with the no-enrichment PCBE strategy, the DisSUGs did not alter the frequency of genome-wide sgRNA-independent off-target mutations, but slightly increased the frequency of target-dependent off-target mutations. Collectively, the DisSUGs developed in this study greatly enhances the efficiency of screening plant base-edited cells and will be a useful system in future applications. 关 键 词:cell ENRICHMENT surrogate REPORTER CYTOSINE BASE EDITORS ADENINE BASE EDITORS
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