Descurainiasophia DsCBF gene, preparation method and application thereof
A technology of Artemisia indica and genes, applied in the field of Artemisia indica DsCBF cold resistance gene and its preparation, can solve the problems of lack of pertinence, effort, and time, and achieve the effect of drought resistance and salt-alkaline resistance
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Embodiment 1
[0026] Example 1 Preparation of Artemisia persicae DsCBF cold resistance gene
[0027] 1. Cloning of the cold resistance gene DsCBF of Artemisia persicae
[0028] (1) The source (Collection) of Artemisia sophia, the seeds of Artemisia sophia were purchased from Chengdu Seed Company, Sichuan Province;
[0029] (2) Isolation of total RNA (RNA isolation)
[0030] Use Trizol reagent to extract the total RNA of Artemisia annua;
[0031] (3) Cloning of Full-length cDNA of DsCBF cold resistance gene of Artemisia persicae
[0032] According to the known conserved amino acid sequences of CBF1, CBF2, and CBF3 of Arabidopsis thaliana; 662 CBFprotein and 663 CBF-like protein of Brassica napus, degenerate primers were designed, and using the principle of homologous gene cloning, the RACE method was used to complete cDNA Long cloning is divided into three stages:
[0033] In the first stage, RT-PCR amplification is performed using degenerate primers and total RNA as a template:
[0034...
Embodiment 2
[0053] Example 2 Construction of Recombinant Plasmid of Artemisia persicae DsCBF Cold Resistance Gene
[0054] According to the full-length sequence of the DsCBF gene of Artemisia indica, primers were designed to amplify its open reading frame, and two restriction enzyme sites BamHI and SacI were respectively introduced into the forward primer and reverse primer to construct the DsCBF gene expression vector; After PCR amplification, the Artemisia persicae DsCBF gene was cloned into the intermediate vector pMD18-T, pMD18-T was digested with restriction enzymes BamHI and SacI, and the DsCBF gene was recovered; the plant expression vector pBI121 was digested with BamHI and SacI, and the pBI121 fragment was recovered ; Insert the DsCBF gene between BamHI and SacI of pBI121 to form the DsCBF gene expression vector pBIcbf; then transfer it into Agrobacterium tumefaciens (Agrobacterium tumefaciens) EHA105 (Pirece, USA), and finally use it to transform the CBF of the model plant defec...
Embodiment 3
[0055] Example 3 Application of the Recombinant Plasmid Expressing the Cold Resistance Gene of Artemisia persicae DsCBF in Arabidopsis
[0056] Use the inflorescence transfection method to transform Arabidopsis thaliana, and transform according to the following steps:
[0057] (1) Planting Arabidopsis until the flowering stage, the soil surface is covered with gauze or cotton cloth;
[0058] (2) remove the terminal inflorescence, to promote the growth of the secondary inflorescence, the plant will grow rapidly in 4-6 days after removing the terminal inflorescence;
[0059] (3) Cultivate Agrobacterium to the logarithmic growth phase at 28°C;
[0060] (4) Centrifuge at 4000rpm, resuspend the bacteria to OD with fresh 5% sucrose solution 600 =0.8; every 2-3 small pots (small pot diameter 9cm) need to be soaked with 400ml-500ml agrobacterium liquid;
[0061] (5) Before dipping, add surfactant Silwet L-77 (500ul / L) and mix well. If Silwet L-77 is too toxic, reduce the concentrat...
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