Apple V-ATPase subunit gene MdVHA-B1S396A and stress-resistance application thereof
A mdvha-b1s396a, apple technology, applied in application, genetic engineering, plant genetic improvement and other directions, can solve the problem of long cycle of resistant varieties
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Embodiment 1
[0069] Example 1: Cloning of apple V-ATPase subunit gene MdVHA-B1.
[0070] 1) Gala tissue culture leaf RNA extraction and reverse transcription
[0071] 1. Extraction of plant total RNA
[0072] Use the RNAplant plus Reagent kit to extract RNA on a small scale (the material is generally a tissue containing more starch and sugar, such as apple tissue, and the sample mass is <0.1g):
[0073] Take less than 0.1g of frozen ground apple tissue material, add 0.5ml kit extraction reagent (4°C), shake until thoroughly mixed;
[0074] 1) Leave at room temperature for 5 minutes. Note: Lay centrifuge tubes flat to maximize surface area;
[0075] 2) Centrifuge at 12,000 rpm for 1 minute at 4°C, and transfer the supernatant to a new RNase-free centrifuge tube;
[0076] 3) Add 0.1ml 5M NaCl and mix gently;
[0077] 4) Add 0.3ml chloroform, mix up and down;
[0078] 5) Centrifuge at 12,000 rpm for 10 minutes at 4°C, take the upper aqueous phase and transfer it to a new RNase-free cent...
Embodiment 2
[0108] Example 2: Apple MdVHA-B1 Gene Chromosomal Location and Genome Structure
[0109] Using the nucleotide sequence of the V-ATPase subunit gene AtVHA-B1 in Arabidopsis thaliana published in the Arabidopsis genome database, the homologous sequence (serial number MDP0000945182) was found in the apple genome database blast. Chromosomal location of the MdVHA-B1 gene uses the genome database of the Apple website (http: / / genomics.research.iasma.it / ); and genome structure prediction uses (http: / / gsds.cbi.pku.edu.cn / index. php) database (attached figure 1 ): The apple V-ATPase subunit gene MdVHA-B1 is located on chromosome 10 near the centromere; it consists of 14 exons and 13 introns.
example 3
[0110] Example 3: Response of MdVHA-B1 gene to salt stress
[0111] (1) Treat the tissue-cultured seedlings of Apple Gala with better growth condition with 100mM NaCl for 0h, 1h, 3h, 6h, 9h, 12h and 24h respectively, and then take samples respectively, fix them rapidly in liquid nitrogen, extract RNA respectively and reverse The cDNA of each sample was obtained by transcription.
[0112] (2) Design specific primers MdVHAB1(RT)-F, MdVHAB1(RT)-R and apple internal reference primers Md18S-F, Md18S-R in the 5' non-coding region of MdVHA-B1 gene.
[0113] Md18S-F: 5'-AAACGGCTACCACATCCA-3', its sequence is shown in SEQ.ID.NO.9;
[0114] Md18S-R: 5'-CACCAGACTTGCCCTCCA-3', its sequence is shown in SEQ.ID.NO.10;
[0115] MdVHAB1(RT)-F: 5'-TCTCTTTCTTCCGCTTGGCTC-3', its sequence is shown in SEQ.ID.NO.11;
[0116] MdVHAB1(RT)-R: 5'-ACAACCGGGTGACAAGCTAAC-3', its sequence is shown in SEQ.ID.NO.12;
[0117] (3) Use the cDNA obtained in step 1) of Example 3 as a template, and adjust these...
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