Sweet potato stem nematode resistance related protein IbPIF1 as well as coding gene and application thereof
A resistance-related, stem nematode technology, applied in application, genetic engineering, plant genetic improvement, etc., to achieve the effects of improved disease resistance, broad application space and market prospects
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Embodiment 1
[0070] Example 1. Obtaining the protein IbPIF1 and its encoding gene related to the improvement of sweet potato stem nematode disease
[0071] 1. Extraction of total RNA from sweet potato
[0072] Take 0.1 g of young leaves of sweet potato variety Lushu No. 3 and grind them into powder in liquid nitrogen, add them to a 2 mL centrifuge tube, and use TIANGEN's RNAprep pure plant total RNA extraction kit (catalog number: DP432) to extract total sweet potato RNA, kit Included: Lysis Buffer RL, Deproteinization Buffer RW1, Wash Buffer RW, RNase-Free ddH 2 O, RNase-Free adsorption column CR3, RNase-Free filter column CS, DNase I, buffer RDD, RNase-Free centrifuge tube, RNase-Free collection tube.
[0073] Take 1 μL of the extracted total RNA to detect its integrity by 1.2% agarose gel electrophoresis, and take another 2 μL of the extracted total RNA to dilute to 500 μL, and use a UV spectrophotometer to detect its quality (OD). 260 ) and purity (OD 260 / OD 280 ), the total RNA e...
Embodiment 2
[0080] Example 2. Application of IbPIF1 protein in improving sweet potato D. nematode resistance
[0081] 1. Preparation of IbPIF1-transformed sweet potato
[0082] 1. Construction of plant expression vector
[0083] 1) According to the coding sequence of the sweet potato IbPIF1 gene, design and amplify the primer sequence of the complete coding sequence, and respectively introduce NcoI and PmlI restriction sites in the forward primer (primer 3) and reverse primer (primer 4), the primers The sequence is as follows:
[0084] Primer 3: 5'- CATGCCATGG ATGGATGAGGACTTCAATCTTCCT-3' (the underlined part is the NcoI restriction site);
[0085] Primer 4: 5'- GCCACGTG TCAACGAGATTGATGATTCCCTG-3' (the underlined part is the PmlI restriction site).
[0086] 2) Take the DNA fragment shown in the artificially synthesized SEQ ID No.2 as template, adopt primer 3 and primer 4 to carry out PCR amplification, obtain PCR product, then PCR product is connected to pMD19-T carrier (purchased f...
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