A kind of cultivation method and application of Arabidopsis xpo1a/xpo1b± double mutant
A technology of m-xpo1a-rp and m-xpo1a-lp, applied in the field of Arabidopsis thaliana, can solve the problems of restricting the use of TuMV-resistant varieties, long cycle, low efficiency, etc., so as to facilitate follow-up scientific research and field application, genetic Effect of clear background and stable antiviral properties
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[0041] A method for cultivating an Arabidopsis xpo1a / xpo1b double mutant, specifically comprising the following steps:
[0042] (1) Obtain the Arabidopsis thaliana xpo1a mutant (Arabidopsis mutant library number: SALK_078639C);
[0043] (2) 20 days after sowing, DNA and RNA were extracted from the leaves of Arabidopsis thaliana plants of the xpo1a mutant by the CTAB method and the Trizol method;
[0044] (3) Utilize the primer pair LBb1.3-F and m-xpo1a-RP, m-xpo1a-LP and m-xpo1a-RP, and use the extracted DNA as a template for PCR amplification to determine the homozygous situation of the xpo1a mutant (due to T - DNA insertion, LBb1.3-F and m-xpo1a-RP can amplify DNA fragments of specific length, but m-xpo1a-LP and m-xpo1a-RP cannot amplify DNA fragments of specific length). The primer sequences used were:
[0045] LBb1.3-F (tcgcttgtgaatattgtgcag)
[0046] m-xpo1a-LP (atcaaggcagggaaacaaaac)
[0047] m-xpo1a-RP (tgggcagaaatcataggacag); as shown in SEQ ID: No.3-5;
[0048] The...
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