Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding/Jiangsu Key Laboratory of Crop Genetics and Physiology, Agricultural College of Yangzhou University, Yangzhou, China.
Jiangsu Co-Innovation Center for Modern Production Technology of Grain Crops, Yangzhou University, Yangzhou, China.
Plant Biotechnol J. 2022 Mar;20(3):499-510. doi: 10.1111/pbi.13732. Epub 2021 Nov 2.
Cytosine base editors (CBEs) can install a predefined stop codon at the target site, representing a more predictable and neater method for creating genetic knockouts without altering the genome size. Due to the enhanced predictability of the editing outcomes, it is also more efficient to obtain homozygous mutants in the first generation. With the recent advancement of CBEs on improved editing activity, purify and specificity in plants and animals, base editing has become a more appealing technology for generating knockouts. However, there is a lack of design tools that can aid the adoption of CBEs for achieving such a purpose, especially in plants. Here, we developed a user-friendly design tool named CRISPR-BETS (base editing to stop), which helps with guide RNA (gRNA) design for introducing stop codons in the protein-coding genes of interest. We demonstrated in rice and tomato that CRISPR-BETS is easy-to-use, and its generated gRNAs are highly specific and efficient for generating stop codons and obtaining homozygous knockout lines. While we tailored the tool for the plant research community, CRISPR-BETS can also serve non-plant species.
胞嘧啶碱基编辑器(CBEs)可以在目标位点引入预设的终止密码子,这代表着一种更可预测、更简洁的方法,可在不改变基因组大小的情况下创建基因敲除。由于编辑结果的可预测性增强,在第一代中获得纯合突变体的效率也更高。由于 CBE 在提高编辑活性、在动植物中的纯度和特异性方面的最新进展,碱基编辑已成为生成敲除的更具吸引力的技术。然而,缺乏能够帮助采用 CBE 实现这一目标的设计工具,特别是在植物中。在这里,我们开发了一种名为 CRISPR-BETS(碱基编辑以停止)的用户友好型设计工具,它有助于设计引导 RNA(gRNA),在感兴趣的蛋白质编码基因中引入终止密码子。我们在水稻和番茄中证明了 CRISPR-BETS 易于使用,其生成的 gRNA 高度特异性和高效,可产生终止密码子并获得纯合敲除系。虽然我们为植物研究界量身定制了该工具,但 CRISPR-BETS 也可用于非植物物种。