A kind of Chunlan cgwrky11 gene and its application
A gene and transgenic technology, applied in Chunlan CgWRKY11 gene and its application fields, can solve the problems of reduced activity, different gene functions, and reduced, and achieve the effect of prolonging the vegetative growth cycle
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Embodiment 1
[0023] The material used in this example is the leaves of Chunlan 'Songmei', which were quickly frozen in liquid nitrogen after harvest and stored in an ultra-low temperature refrigerator (-80°C).
[0024] 1) Extraction of total RNA from Chunlan leaves
[0025] Follow the instructions of the TaKaRa Plant Total RNA Extraction Kit. The specific operations are:
[0026] The cryopreserved Chunlan leaves were quickly transferred to a mortar pre-cooled with liquid nitrogen, and the tissue was ground with a pestle, during which liquid nitrogen was continuously added until it was ground into powder; Buffer PE into a 1.5 mL sterilized tube, pipette repeatedly until there is no obvious precipitation in the lysate; centrifuge the lysate at 12,000 rpm at 4°C for 5 min; carefully pipette the supernatant into a new 1.5 mL sterilized tube . Add 1 / 10 volume of Buffer NB to the supernatant, mix with Vortex, centrifuge at 12,000 rpm and 4°C for 5 min; carefully pipette the supernatant into a ...
Embodiment 2
[0048] Research indicates WRKY11 The gene is expressed in various tissues and organs in Chunlan ( figure 2 a), but the expression of this gene is the highest in spring orchid, indicating that the gene is functionally active in flowers. Through the expression analysis of the leaves treated with ABA stress of Chunlan ( figure 2 b), to prove CgWRKY11 The gene plays an important regulatory role in the ABA stress response of Chunlan leaves.
[0049] The plant material used in this example is Arabidopsis ( Arabidopsis thaliana ) Col (Columbia) wild-type seeds.
[0050] The Escherichia coli strain used in this example was Trans5α; the Agrobacterium strain was GV3101, which were respectively used to transform Arabidopsis thaliana; the plant expression vector used in the experiment was pBI121. The strains used were purchased from Quanjin Bio and Price Bio.
[0051] 1) CgWRKY11 Construction of gene overexpression vector
[0052] obtained in Example 1 CgWRKY11 The full-lengt...
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