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首页> 外文期刊>Journal of Experimental Botany >Efficient induction of haploid plants in wheat by editing of TaMTL using an optimized Agrobacterium-mediated CRISPR system
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Efficient induction of haploid plants in wheat by editing of TaMTL using an optimized Agrobacterium-mediated CRISPR system

机译:通过优化的农杆菌介导的CRISPR系统编辑TAMTL,高效诱导小麦的单倍体植物

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摘要

The use of CRISPR/LbCpf1 and CRISPR/xCas9 systems in wheat have not yet been reported. In this study, we compared the efficiencies of three CRISPR editing systems (SpCas9, LbCpf1, and xCas9), and three different promoters (OsU6a, TaU3, and TaU6) that drive single-guide (sg)RNA, which were introduced into wheat via Agrobacterium-mediated transformation. The results indicated that TaU3 was a better choice than OsU6a or TaU6. The editing efficiency was higher using two sgRNAs than one sgRNA, and mutants with a large fragment deletion between the two sgRNAs were produced. The LbCpf1 and xCas9 systems could both be used successfully. Two endogenous genes, TaWaxy and TaMTL, were edited with high efficiency by the optimized SpCas9 system, with the highest efficiency (80.5%) being achieved when using TaU3 and two sgRNAs to target TaWaxy. Rates of seed set in the TaMTL-edited T-0 transgenic plants were much lower than that of the wild-type. A haploid induction rate of 18.9% was found in the TaMTL-edited T-1 plants using the CRISPR/SpCas9 system. Mutants with reverse insertion of the deleted sequences of TaMTL and TaWaxy between the two sgRNAs were identified in the edited T-0 plants. In addition, wheat grains lacking embryos or endosperms were observed in the TaMTL-edited T-1 generation.
机译:尚未报告使用CRISPR / LBCPF1和CRISPR / XCAS9系统。在这项研究中,我们比较了三种CRISPR编辑系统(SPCAS9,LBCPF1和XCAS9)的效率,以及驱动单引导(SG)RNA的三种不同的启动子(OSU6a,TAU3和TAU6),该RNA通过农杆菌介导的转化。结果表明,TAU3是比OSU6A或TAU6更好的选择。使用两个SGRNA的编辑效率高于一个SGRNA,并产生两个SGRNA之间的突变体缺失的突变体。 LBCPF1和XCAS9系统均可成功使用。通过优化的SPCAS9系统以高效率编辑了两个内源性基因,Tawaxy和Tamtl,使用TAU3和两个SGRNA靶向raTaxy时,实现了最高效率(80.5%)。在棕褐色编辑的T-0转基因植物中设置的种子率远低于野生型的速率。使用CRISPR / SPCAS9系统,在Tamtl编辑的T-1植物中发现了18.9%的单倍体诱导速率。在编辑的T-0植物中鉴定了具有反向插入缺失的TAMT1和Tawaxy的缺失序列的突变体。此外,在TamT1编辑的T-1代代中观察到缺乏胚胎或胚乳的小麦颗粒。

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