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Allele exchange at the EPSPS locus confers glyphosate tolerance in cassava

机译:Epsps基因座的等位基因交换赋予了木薯的草甘膦耐受性

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Effective weed control can protect yields of cassava (Manihot esculenta) storage roots. Farmers could benefit from using herbicide with a tolerant cultivar. We applied traditional transgenesis and gene editing to generate robust glyphosate tolerance in cassava. By comparing promoters regulating expression of transformed 5‐enolpyruvylshikimate‐3‐phosphate synthase (EPSPS) genes with various paired amino acid substitutions, we found that strong constitutive expression is required to achieve glyphosate tolerance during in?vitro selection and in whole cassava plants. Using strategies that exploit homologous recombination (HR) and nonhomologous end‐joining (NHEJ) DNA repair pathways, we precisely introduced the best‐performing allele into the cassava genome, simultaneously creating a promoter swap and dual amino acid substitutions at the endogenous EPSPS locus. Primary EPSPS‐edited plants were phenotypically normal, tolerant to high doses of glyphosate, with some free of detectable?T‐DNA integrations. Our methods demonstrate an editing strategy for creating glyphosate tolerance in crop plants and demonstrate the potential of gene editing for further improvement of cassava.
机译:有效的杂草控制可以保护Cassava(Manihot Esculenta)储存根的产量。农民可以从使用除草剂具有耐培养品种的利益。我们应用传统的转子和基因编辑,以产生木薯的鲁棒草甘膦耐受性。通过将调节转化的5-烯醇吡咯的3-磷酸合酶(EPSPS)基因的启动子与各种成对的氨基酸取代进行比较,我们发现需要强烈的组成型表达来在体外选择和整个木薯植物中实现草甘膦耐受性。使用利用同源重组(HR)和非博学终端接合(NHEJ)DNA修复途径的策略,我们将最佳性能的等位基因与Cassava基因组共同引入,同时在内源性Epsps基因座中产生启动子换水和双氨基酸取代。主要EPSPS编辑植物是表型正常的,耐高量的草甘膦,一些不可检测的ΔT-DNA集成。我们的方法证明了用于在作物植物中产生草甘膦耐受性的编辑策略,并证明基因编辑的潜力进一步改善木薯。

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