A wheat powdery mildew resistance-related protein tawrky49 and its coding gene and application
A technology related to wheat powdery mildew and resistance, which can be used in application, genetic engineering, plant genetic improvement, etc., and can solve problems such as scarcity
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Embodiment 1
[0040] Embodiment 1, TaWRKY49 Gene acquisition
[0041] 1. Obtaining RNA
[0042] The 7-day seedlings of wheat variety Shannong 20 were inoculated with Erysiphysis tritici physiological race E09, and the samples were collected for 48 hours to extract RNA.
[0043] 2. Obtain cDNA by reverse transcription
[0044] Reverse transcription system:
[0045] RNA 2.5 μL, Oligo-dT primer 1 μL, DEPC water 6.5 μL, mix the above solutions in a centrifuge tube, incubate at 65°C for 5 minutes, and place on ice for another 5 minutes.
[0046] Then add 5 μL of 5× reverse transcription buffer solution, 1.25 μL of dNTP mix, 0.625 μL of inhibitor, 1 μL of M-MLV reverse transcriptase, 7.125 μL of DEPC water to the above system, incubate at 42°C for 1 hour, and incubate at 95°C for 5 minutes. cDNA was obtained.
[0047] 3. Clone TaWRKY49
[0048] Add the above cDNA to 25 μL double distilled water, take 1 μL for subsequent PCR reaction as a template, and use the following primers for PCR am...
Embodiment 2
[0054] Embodiment 2, TaWRKY49 Application of Genes in Resistance to Powdery Mildew
[0055] 1. Identification of the regulatory role of TaWRKY49 on wheat powdery mildew resistance by gene gun transient overexpression technology
[0056] 1. Carrier Construction
[0057] 1) Using the PCR product obtained in Example 1 (or the artificially synthesized sequence 1) as a template, perform PCR amplification with the following primers to obtain a PCR product of about 1.2Kb.
[0058] Forward primer: GGGGACAAGTTTGTACAAAAAAGCAGGCTTCATGGCATCTTGTGGCGGC (SEQ ID No. 5)
[0059] Reverse primer: GGGGACCACTTTGTACAAGAAAGCTGGGTCTCATAAAAAAATATTACTAC (SEQ ID No. 6)
[0060] 2) Use the PCR product obtained in step 1) to perform BP reaction with the pDNOR201 vector (purchased from Invitrogen) to obtain the ENTRY vector.
[0061] The above BP reaction system: PCR product 75ng, pDNOR201 75ng, BPase 0.5 μL, overnight at 25°C.
[0062] 3) Perform LR reaction between the above ENTRY vector and pUbi-A...
Embodiment 3
[0113] Example 3. Analysis of subcellular localization of TaWRKY49 and expression pattern induced by powdery mildew
[0114] 1. Subcellular localization of TaWRKY49
[0115] 1. Carrier Construction
[0116] 1) Using the PCR product obtained in Example 1 (or the artificially synthesized sequence 1) as a template, perform PCR amplification with the following primers to obtain a PCR product of about 1.2Kb.
[0117] Forward primer: GGGGACAAGTTTGTACAAAAAAGCAGGCTTCATGGCATCTTGTGGCGGCG (SEQ ID No. 9)
[0118] Reverse primer: GGGGACCACTTTGTACAAGAAAGCTGGGTCTAAAAAAAATATTACTACTAC (SEQ ID No. 10)
[0119] 2) Use the PCR product prepared in step 1) to perform BP reaction with the pDNOR201 vector (purchased from Invitrogen) to obtain the ENTRY-TaWRKY49 vector.
[0120] The above BP reaction system: PCR product 75ng, pDNOR201 75ng, BPase 0.5μL, overnight at 25°C.
[0121] 3) React the above ENTRY-TaWRKY49 vector with pUbi-Gateway-mYFP vector LR to generate pUbi-TaWRKY49-mYFP vector.
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