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Generation of alpha-solanine-free hairy roots of potato by CRISPR/Cas9 mediated genome editing of the St16DOX gene

机译:通过CRISPR / CAS9介导的ST16DOX基因的CRACR / CAS9介导的基因组编辑α-Solanine的毛茸茸根的产生

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Potato (Solanum tuberosum) is a major food crop, while the most tissues of potato accumulates steroidal glycoalkaloids (SGAs) alpha-solanine and alpha-chaconine. Since SGAs confer a bitter taste on human and show the toxicity against various organisms, reducing the SGA content in the tubers is requisite for potato breeding. However, generation of SGA-free potato has not been achieved yet, although silencing of several SGA biosynthetic genes led a decrease in SGAs. Here, we show that the knockout of St16DOX encoding a steroid 16 alpha-hydroxylase in SGA biosynthesis causes the complete abolition of the SGA accumulation in potato hairy roots. Nine candidate guide RNA (gRNA) target sequences were selected from Stl6DOX by in silico analysis, and the two or three gRNAs were introduced into a CRISPR/Cas9 vector designated as pMgP237-2A-GFP that can express multiplex gRNAs based on the pre-tRNA processing system. To establish rapid screening of the candidate gRNAs that can efficiently mutate the St16DOX gene, we used a potato hairy root culture system for the introduction of the pMgP237 vectors. Among the transgenic hairy roots, two independent lines showed no detectable SGAs but accumulated the glycosides of 22,26-dihydroxycholesterol, which is the substrate of St16DOX. Analysis of the two lines with sequencing exhibited the mutated sequences of St16DOX with no wild-type sequences. Thus, generation of SGA-free hairy roots of tetraploid potato was achieved by the combination of the hairy root culture and the pMgP237-2A-GFP vector. This experimental system is useful to evaluate the efficacy of candidate gRNA target sequences in the short-term.
机译:土豆(Solanum Tuberosum)是一种主要的食物作物,而马铃薯的大多数组织积累了甾体甘油碱(SGAS)α-甲烷和α-亚基酮。由于SGAS赋予人类苦味并且表现出对各种生物的毒性,降低块茎中的SGA含量是马铃薯育种的必要条件。然而,尚未实现SGA的马铃薯的产生,尽管几个SGA生物合成基因的沉默导致SGA的减少。在这里,我们表明,在SGA生物合成中编码类固醇16α-羟化酶的ST16Dox的敲除导致马铃薯毛根的SGA积累完全取消了SGA积累。九个候选引导RNA(GRNA)靶序列由STL6DOX选择在STL6DOX中,将两种或三个GRNA引入指定为PMGP237-2A-GFP的CRISPR / CAS9载体中,其可以基于Pre-TRNA表达多重GRNA处理系统。为了建立能够有效突变ST16Dox基因的候选GRNA的快速筛选,我们使用了马铃薯毛的根培养系统来引入PMGP237载体。在转基因毛状根中,两个独立的线显示出可检测的SGA,但累积了22,2,26-二羟基胆固醇的糖苷,即ST16Dox的基材。用测序的两条线分析表现出ST16Dox的突变序列,没有野生型序列。因此,通过毛状根培养物和PMGP237-2A-GFP载体的组合实现了四倍吡喃丙酯的无甲状腺马铃薯的产生的产生。该实验系统可用于评估候选GRNA靶序列在短期内的疗效。

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