Expanding the range of CRISPR/Cas9-directed genome editing in soybean

IF 4.6 4区 农林科学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY aBIOTECH Pub Date : 2021-06-25 DOI:10.1007/s42994-021-00051-4
Reqing He, Pengxiang Zhang, Yuchuan Yan, Chen Yu, Liyun Jiang, Youlin Zhu, Dong Wang
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引用次数: 2

Abstract

The CRISPR/Cas9 system has been widely applied for plant genome editing. The commonly used SpCas9 has been shown to rely on the protospacer adjacent motif (PAM) sequences in the canonical form NGG and non-canonical NAG. Although these PAM sequences are extensively distributed across plant genomes, a broader scope of PAM sequence is required to expand the range of genome editing. Here we report the adoption of three variant enzymes, xCas9, SpCas9-NG and XNG-Cas9, to produce targeted mutation in soybean. Sequencing results determined that xCas9 with the NGG and KGA (contains TGA and GGA) PAMs successfully induces genome editing in soybean genome. SpCas9-NG could recognize NGD (contains NGG, NGA and NGT), RGC (contains AGC and GGC), GAA and GAT PAM sites. In addition, XNG-Cas9 was observed to cleave soybean genomic regions with NGG, GAA and AGY (contains AGC and AGT) PAM. Moreover, off-target analyses on soybean editing events induced by SpCas9 and xCas9 indicated that two high-fidelity Cas9 variants including eSpCas9 (enhanced specificity SpCas9) and exCas9 (enhanced specificity xCas9) could improve the specificity of the GGA PAM sequence without reducing on-target editing efficiency. These findings significantly expand the scope of Cas9-mediated genome editing in soybean.

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扩大CRISPR/Cas9指导的大豆基因组编辑范围
CRISPR/Cas9系统已广泛应用于植物基因组编辑。常用的SpCas9已被证明依赖于典型形式NGG和非典型NAG的原间隔基相邻基序(PAM)序列。尽管这些PAM序列广泛分布在植物基因组中,但需要更广泛的PAM序列来扩大基因组编辑的范围。在这里,我们报道了采用三种变体酶,xCas9、SpCas9-NG和XNG-Cas9,在大豆中产生靶向突变。测序结果表明,含有NGG和KGA(含有TGA和GGA)PAMs的xCas9成功诱导了大豆基因组的基因组编辑。SpCas9-NG能识别NGD(包含NGG、NGA和NGT)、RGC(包含AGC和GGC)、GAA和GAT-PAM位点。此外,观察到XNG-Cas9用NGG、GAA和AGY(包含AGC和AGT)PAM切割大豆基因组区域。此外,对SpCas9和xCas9诱导的大豆编辑事件的脱靶分析表明,包括eSpCas9(增强特异性SpCas9)和exCas9(增强特异性xCas9)在内的两种高保真Cas9变体可以在不降低靶上编辑效率的情况下提高GGA-PAM序列的特异性。这些发现显著扩大了Cas9介导的大豆基因组编辑的范围。
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CiteScore
7.70
自引率
2.80%
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0
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