清脆的
基因组编辑
核酸酶
效应器
Cas9
DNA
基因组
基因组工程
CRISPR干扰
计算生物学
锌指核酸酶
引导RNA
转录激活物样效应核酸酶
生物
遗传学
细胞生物学
同源重组
基因靶向
核酸内切酶
分子生物学
基因
作者
Greta Bigelyte,Joshua K. Young,Tautvydas Karvelis,Karolina Budre,Rimantė Žedaveinytė,Vesna Djukanovic,Elizabeth Van Ginkel,Sushmitha Paulraj,Stephen L. Gasior,Spencer Jones,Lanie Feigenbutz,Grace St. Clair,Pierluigi Barone,Jennifer A. Bohn,Ananta Acharya,Gina Zastrow‐Hayes,Selgar Henkel-Heinecke,Arūnas Šilanskas,Ralf Seidel,Virginijus Šikšnys
标识
DOI:10.1038/s41467-021-26469-4
摘要
Class 2 CRISPR systems are exceptionally diverse, nevertheless, all share a single effector protein that contains a conserved RuvC-like nuclease domain. Interestingly, the size of these CRISPR-associated (Cas) nucleases ranges from >1000 amino acids (aa) for Cas9/Cas12a to as small as 400-600 aa for Cas12f. For in vivo genome editing applications, compact RNA-guided nucleases are desirable and would streamline cellular delivery approaches. Although miniature Cas12f effectors have been shown to cleave double-stranded DNA, targeted DNA modification in eukaryotic cells has yet to be demonstrated. Here, we biochemically characterize two miniature type V-F Cas nucleases, SpCas12f1 (497 aa) and AsCas12f1 (422 aa), and show that SpCas12f1 functions in both plant and human cells to produce targeted modifications with outcomes in plants being enhanced with short heat pulses. Our findings pave the way for the development of miniature Cas12f1-based genome editing tools.
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