Gene editing method for aroma control gene of improved indica rice strain and application thereof
A gene editing and gene technology, applied in the field of crops, to achieve the effect of efficient gene editing
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Embodiment 1
[0081] 1. Construction of gene editing transformation vector KF80:
[0082] Gene editing based on Streptococcus pyogenes acquired immune system CRISPR endonuclease Cas9 has been achieved in a variety of plants, and the NHEJ editing efficiency is often as high as 90%. Refer to the design of gene editing Agrobacterium transformation vector pHSE401 (Xing et al. , 2014, BMC Plant Biol 14:327), through the use of monocotyledonous plant-specific maize ubiquitin gene promoter ZmUBI1 pro and a maize U6 snRNA gene promoter ZmU6 pro, respectively for high-efficiency expression in grasses such as rice and maize Cas9 and gRNA genes, the final Agrobacterium transformation DNA binary vector for gene editing consists of three gene expression units ZmU6 pro:gRNA:AtU6-26 term, ZmUBI1 pro:SpCas9:PsE9 term, and 35S pro:HygR:35S term , There is a BsaI restriction site between ZmU6 pro and gRNA, and any gRNA sequence can be inserted using DNA ligase or Gibson cloning method after the vector is lin...
Embodiment 2
[0117] 1. Construction of gene editing transformation vector KF80:
[0118]Gene editing based on Streptococcus pyogenes acquired immune system CRISPR endonuclease Cas9 has been achieved in a variety of plants, and the NHEJ editing efficiency is often as high as 90%. Refer to the design of gene editing Agrobacterium transformation vector pHSE401 (Xing et al. , 2014, BMC Plant Biol 14:327), through the use of monocotyledonous plant-specific maize ubiquitin gene promoter ZmUBI1 pro and a maize U6 snRNA gene promoter ZmU6 pro, respectively for high-efficiency expression in grasses such as rice and maize Cas9 and gRNA genes, the final Agrobacterium transformation DNA binary vector for gene editing consists of three gene expression units ZmU6 pro:gRNA:AtU6-26 term, ZmUBI1pro:SpCas9:PsE9 term and 35S pro:HygR:35S term, There is a BsaI restriction site between ZmU6 pro and gRNA, and any gRNA sequence can be inserted using DNA ligase or Gibson cloning method after the vector is lineari...
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