Graduate School of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai-cho, Nada-ku, Kobe, Hyogo, 657-8501, Japan.
Graduate School of Agriculture, Meijo University, 1-501 Shiogamaguchi, Tempaku-ku, Nagoya, Aichi, 468-8502, Japan.
Plant Physiol Biochem. 2018 Oct;131:78-83. doi: 10.1016/j.plaphy.2018.04.028. Epub 2018 Apr 25.
The CRISPR/Cas9 system is a revolutionary genome-editing tool for directed gene editing in various organisms. Cas9 variants can be applied as molecular homing devices when combined with various functional effectors such as transcriptional activators or DNA modification enzymes. Target-AID is a synthetic complex of nuclease deficient Cas9 fused to an activation-induced cytidine deaminase (AID) that enables targeted nucleotide substitution (C to T or G to A). We previously demonstrated that the introduction of desired point mutations into target genes by Target-AID confers herbicide tolerance to rice callus. Inheritance of the introduced mutations, as well as the removal of transgenes, are key issues that must be addressed in order to fully develop Target-AID as a plant breeding technique. Here we report the transmission of such mutations from the callus to regenerants and their progenies, leading to a generation of selectable marker-free (SMF) herbicide tolerant rice plants with simultaneous multiplex nucleotide substitutions. These findings demonstrate that Target-AID can be developed into novel plant breeding technology which enables improvement of multiplex traits at one time in combination with sophisticated targeted base editing with the simplicity and versatility of CRISPR/Cas9 system.
CRISPR/Cas9 系统是一种用于各种生物中定向基因编辑的革命性基因组编辑工具。当 Cas9 变体与各种功能效应器(如转录激活因子或 DNA 修饰酶)结合使用时,可以作为分子归巢装置。Target-AID 是一种由无核酸酶 Cas9 融合到激活诱导胞嘧啶脱氨酶(AID)的合成复合物,可实现靶向核苷酸取代(C 到 T 或 G 到 A)。我们之前证明,通过 Target-AID 将所需的点突变引入靶基因可赋予水稻愈伤组织对除草剂的耐受性。为了充分将 Target-AID 开发为一种植物育种技术,必须解决引入突变的遗传以及转基因的去除等关键问题。在这里,我们报告了这种突变从愈伤组织传递到再生体及其后代,并导致产生可选择标记自由(SMF)的除草剂耐受水稻植物,同时具有多重核苷酸取代。这些发现表明,Target-AID 可以开发成为一种新型的植物育种技术,它可以与 CRISPR/Cas9 系统的简单性和多功能性相结合,同时改进多个性状的复杂靶向碱基编辑。