Wheat powdery mildew resistance associated protein TaEDS1-B1 and encoding gene and application thereof
A technology of powdery mildew and coding, applied in the fields of application, genetic engineering, plant genetic improvement, etc., can solve the problems such as loss of resistance of production varieties
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Embodiment 1
[0089] Example 1. Cloning and sequence structure analysis of wheat TaEDS1-B1 gene
[0090] 1. Acquisition of cDNA and genomic DNA sequences of the coding region of wheat TaEDS1-B1 gene
[0091] 1. Extraction of wheat genomic DNA and total RNA
[0092] (1) Extraction of wheat genomic DNA
[0093] Wheat genomic DNA was extracted according to the conventional CTAB method. The specific steps are as follows: take about 0.2 g of fresh leaves of 7-day-old Piedea chinensis seedlings, grind them into fine powder in liquid nitrogen, and transfer them to a sterilized 2 ml centrifuge tube. Add 1.0ml CTAB extraction buffer (1.3%CTAB, 133mM Tris / HCl pH8.0, 13mM EDTA, 0.93M NaCl, 0.66%PVP3600, 0.18Mβ-mercaptoethanol), and mix well. Incubate at 65°C for 1.0 h, during which the samples are mixed from time to time to fully extract. After the sample was cooled to room temperature, 1ml of chloroform / isoamyl alcohol (v / v=24:1) was added, and mixed by inversion for 1h. Centrifuge at 12000 rpm ...
Embodiment 2
[0111] Example 2. Using VIGS technology to verify the powdery mildew resistance function of TaEDS1-B1 gene
[0112] 1. Obtaining of TaEDS1-B1 Gene Silenced Plants
[0113] 1. Construction of BSMV-VIGS vector system for inducing TaEDS1-B1 gene
[0114] (1) Acquisition of Silent Sequence
[0115] 1) Obtaining the silence sequence TaEDS1-S1
[0116] Using the recombinant plasmid pGEM-T-TaEDS1-B1 prepared in Example 1 as a template, PCR amplification was performed on TaEDS1-S1F and TaEDS1-S1R using primers to obtain a PCR amplification product of 292bp (corresponding to sequences 1 to 5 ' from the 1133-1424th nucleotide sequence) and named it as the silent sequence TaEDS1-S1.
[0117] The nucleotide sequences of the above-mentioned primers to TaEDS1-S1-F and TaEDS1-S1-R are as follows (the sequence shown in the underline is the restriction endonuclease NheI enzyme cutting recognition site):
[0118] TaEDS1-S1-F:5'-TAC GCTAGC GTGGCCTTGAACTGAG-3';
[0119] TaEDS1-S1-R:5'-TAC ...
Embodiment 3
[0160] Example 3. The function of TaEDS1-B1 was verified by the transient expression technology of wheat leaf epidermal cells
[0161] The function of wheat powdery mildew resistance is an autonomous behavior of single cells, and powdery mildew only infects the epidermal cells of the host leaves. Therefore, transient expression in epidermal cells is an effective technique to verify the function of wheat powdery mildew resistance genes. The target gene was randomly introduced into the epidermal cells of isolated wheat leaves through a gene gun, and a reporter gene was co-transformed at the same time to mark the positively transformed cells. Effect of disease-associated gene expression on powdery mildew infection. The specific implementation steps are as follows:
[0162] 1. Construction of transient expression vectors in epidermal cells of wheat leaves
[0163] 1) Using the pGEM-T-TaEDS1-B1 plasmid prepared in Example 1 as a template, using TaEDS1-B166-NcoI-f3 and TaEDS1-B16...
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