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Genome editing in PDS genes of tomatoes by non-selection method and of Nicotiana benthamiana by one single guide RNA to edit two orthologs

机译:通过非选择方法和尼古利亚纳·宾夕法尼亚州的番茄PDS基因编辑一个单一导向RNA编辑两种矫形器

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The CRISPR/Cas9 system is widely used for targeted mutagenesis in many organisms including plants. For application of this system, tissue culture methods need to be established. In this study, detailed methods for introduction of mutations in tomato and Nicotiana benthamiana plants using the CRISPR/Cas9 system are described. The methods include tissue culture protocols for tomato and N. benthamiana . We also demonstrate the methodology to generate Cas9-free genome edited tomato plants and use of one single guide RNA (sgRNA) to edit two orthologs in N. benthamiana . The examples of editing the PHYTOENE DESATURASE ( PDS ) genes in these plants are also provided. The Cas9-free tomato line was obtained when tomato plants were cultured on a non-selective medium after transformation with the CRISPR/Cas9 system. Two orthologs of PDS in N. benthamiana were mutated using a sgRNA, because these orthologs contain the same nucleotide sequences with PAM motif. These mutations were inherited to the next generation. The mutations in the PDS genes resulted in an albino phenotype in tomato and N. benthamiana plants. These results demonstrate that the non-selective method is one of the ways to obtain Cas9-free genome editing in tomato plants and that the two orthologs can be edited by one sgRNA in N. benthamiana .
机译:CRISPR / CAS9系统广泛用于许多生物体中的靶向诱变。对于该系统的应用,需要建立组织培养方法。在这项研究中,描述了使用CRISPR / CAS9系统引入番茄和尼古利亚纳·尼加沙米亚纳植物中的详细方法。该方法包括番茄和N.Nenthamiana的组织培养方案。我们还展示了产生Cas9无基因组的番茄植物的方法,并使用一种单一引导RNA(SGRNA)来编辑N.Benthamiana的两种原果。还提供了在这些植物中编辑植物去饱和酶(PDS)基因的实施例。在用CRISPR / CAS9系统转化后在非选择性培养基上培养番茄植物时,获得了无CAS9的番茄线。使用SGRNA突变N.Benthamiana中的两个PDS的两个原因,因为这些矫形器含有与PAM基序的相同核苷酸序列。这些突变被遗传到下一代。 PDS基因中的突变导致番茄和N.Penthamiana植物中的白化表型。这些结果表明,非选择性方法是在番茄植物中获得无需基因组的方法之一,并且两种原果可以在N必需的N必需植物中的一个SGRNA编辑。

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