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CRISPR/Cas9 genome editing of rubber producing dandelion Taraxacum kok-saghyz using Agrobacterium rhizogenes without selection

机译:使用发根农杆菌无选择地对生产橡胶的蒲公英蒲公英进行CRISPR / Cas9基因组编辑

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CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats/CRISPR associated protein 9) is a highly accessible genome editing tool. Here we demonstrate its potential for use in Taraxacum species. Taraxacum kok-saghyz (TK, Rubber Dandelion) is notable for its ability to produce high molecular weight rubber in its roots and promise as an alternative source of natural rubber. In order to accelerate the domestication of TK, we have established a simple strategy to deploy CRISPR/Cas9 in this species. A critical gene encoding fructan:fructan 1-fructosyltransferase (1-FFT), implicated in inulin biosynthesis was selected as the target, as inulin is an expected antagonist of rubber production. TK plantlets were inoculated with Agrobacterium rhizogenes harboring a plasmid encoding a Cas9 and sgRNA (single guide RNA) targeting TK 1-FFT. We were able to rapidly induce hairy roots harboring knockout alleles without the selection of stable, herbicide or antibiotic resistant transformants. Mutagenesis was affirmed by observing a loss of restriction sites within 1-FFT, followed by sequencing. Of 11 hairy root samples tested, 10 showed the presence of genome editing, with mutation rates as high as 88.9%, suggesting a high efficiency mutagenesis induced by CRISPR/Cas9 via A. rhizogenes-mediated transformation. Whole TK plants were regenerated from hairy roots harboring knockout alleles. The regenerated plants contained knockout alleles, with mutation rates as high as 80.0%. TK plants with edited genomes were obtained within 10 weeks. By omitting a selection step, it was possible to generate edited TK plants lacking stably transformed CRISPR elements, which may potentially reduce off-target mutagenesis. Application of high efficiency CRISPR/Cas9 genome editing will facilitate the domestication and commercialization of TK as a rubber producing crop, and may accelerate basic research on the regulation of rubber biosynthesis. (C) 2016 Elsevier B.V. All rights reserved.
机译:CRISPR / Cas9(聚簇的规则间隔的短回文重复序列/ CRISPR相关蛋白9)是一种易于使用的基因组编辑工具。在这里,我们证明了其在蒲公英属物种中使用的潜力。蒲公英(TK,Rubber Dandelion)以其在根部生产高分子量橡胶的能力而著称,并有望作为天然橡胶的替代来源。为了加速传统知识的驯化,我们建立了一个简单的策略来在该物种中部署CRISPR / Cas9。选择与菊糖生物合成有关的编码果聚糖:果聚糖1-果糖基转移酶(1-FFT)的关键基因作为靶标,因为菊糖是橡胶生产的预期拮抗剂。用发根农杆菌接种TK小植株,所述发根农杆菌含有编码靶向TK 1-FFT的Cas9和sgRNA(单向导RNA)的质粒。我们能够快速诱导出具有剔除等位基因的毛根,而无需选择稳定的除草剂或抗生素抗性转化子。通过观察1-FFT内限制性酶切位点的缺失,然后进行测序,可以确认突变的发生。在测试的11个毛状根样品中,有10个显示存在基因组编辑,突变率高达88.9%,表明CRISPR / Cas9通过发根农杆菌介导的转化诱导了高效诱变。整个TK植物从带有剔除等位基因的毛根再生。再生的植物含有敲除的等位基因,突变率高达80.0%。在10周内获得了具有经过编辑的基因组的TK植物。通过省略选择步骤,可以生成缺少稳定转化的CRISPR元件的经过编辑的TK植物,这可能会减少脱靶诱变。高效的CRISPR / Cas9基因组编辑技术的应用将促进TK作为橡胶生产作物的驯化和商业化,并可能加快橡胶生物合成调控的基础研究。 (C)2016 Elsevier B.V.保留所有权利。

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