Wheat leaf developmental gene TaWRKY76 and application thereof
A gene and leaf technology, applied to the leaf development gene-WRKY transcription factor TaWRKY76 and its application field, can solve the problems of unclear regulation mechanism of AtIAMT1 and unreported role of WRKY gene.
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Embodiment 1
[0028] Embodiment 1: Cloning of TaWRKY76 gene
[0029] 1.1 Wheat cultivation: germinate Shanrong 3 and Jinan 177 wheat seeds, use Hoagland culture medium, 21 ℃, long-day sunshine (light 16h / darkness 8h), culture to 2 leaves 1 heart stage, and extract RNA;
[0030] 1.2 Extraction of total RNA:
[0031] Reagents and utensils: RNAiso (TaKaRa), chloroform (Chloroform), isopropyl alcohol (Isopropyl alcohol), absolute ethanol (Ethanol), DEPC water, all plastic consumables are treated with DEPC water for 24 hours, 123 ° C, 40 min high pressure damp heat Bacteria, and then dried in an oven at 65°C (about 2 days), glassware and metal utensils were treated at 180°C for 6 hours.
[0032] 1) Material collection: 0.05g of leaves and 0.07g of roots (absorbed with absorbent paper before material collection) were put into a 2ml plastic centrifuge tube, a steel column was added, quick-frozen in liquid nitrogen, and oscillated and ground by an oscillator;
[0033] 2) Add 1.5ml Trizol extract,...
Embodiment 2
[0113] Example 2: Expression profile analysis of TaWRKY76 gene
[0114] 2.1 Material collection: Cultivate Wheat Shanrong 3 and Jinan 177 to the stage of two leaves and one heart according to the method in 1.1, and extract the total RNA of leaves and roots respectively;
[0115] 2.2 Extraction of total RNA, digestion of DNA and reverse transcription of RNA: see 1.2-1.4 for the method
[0116] 2.3 Adjustment of internal reference for semi-quantitative analysis:
[0117] Using cDNA as a template, carry out PCR reaction, the system is slightly modified from 1.5. Primers are as follows
[0118] TaAct-S: 5'-GTTCCAATCTATGAGGGATACACGC-3'
[0119] TaAct-A:5'-GAACCTCCACTGAGAACAACATTACC-3'
[0120] Adjust the internal reference of all samples to a consistent level;
[0121] 2.4 TaWRKY76 gene expression profile analysis: use the above cDNA as a template, and use TaWRKY76 semi-quantitative primers for PCR amplification, and the system is slightly modified from 2.3;
[0122] 2.5 Elec...
Embodiment 3
[0123] Example 3: Subcellular Subcellularization of the TaWRKY76 Gene
[0124] 3.1 Biolistic transformation of onion epidermal cells
[0125] 3.1.1 Preparation of onion skin
[0126] Buy fresh onions from the market, culture them in water for two days until they grow new roots, cut off the inner epidermis (3×3cm) with tweezers and a blade in an ultra-clean bench, spread the inner layer on 1 / 2MS with the inner layer facing down, try not to leave with bubbles,
[0127] 3.1.2 Preparation of particle bullets
[0128] 1) Sterilize twice with 70% alcohol lotion tungsten powder, add 50% sterilized glycerin to make the concentration reach 60mg / ml;
[0129] 2) Mix the tungsten powder particle solution well before use, take 25μl into a 1.5ml centrifuge tube, and then add
[0130] 10 μl plasmid DNA (2 μg / μl),
[0131] 100μl 2.5mol / L CaCl 2 ,
[0132] 40μl 0.1mol / L spermidine, shake while adding;
[0133]3) The mixture was vortexed for 3 minutes;
[0134] 4) Stand still for 1min;...
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