Application of potato StABL1 gene in regulation and control of potato maturity
A potato and gene technology is applied in the field of molecular genetics and breeding to achieve the effect of promoting tuber formation
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Embodiment 1
[0028] This example provides a method for obtaining the transcription factor StABL1 gene associated with potato tuber development.
[0029] Class A bZIP family members in potato have functional redundancy and have SAP motifs that can interact with StSP6A (Teo et al., 2017), screened based on protein interactions (see figure 1 ), we found that StABI5like1, a member of the AREB / ABF / ABI5 subfamily, can interact with StSP6A, and its expression level is high in various developmental organs. Therefore, it is speculated that this gene may also be involved in the growth and development of potato, and we named the gene StABL1.
Embodiment 2
[0031] This embodiment provides the potato StABL1 gene, a cloning method and a function verification method, which specifically include the following steps:
[0032] (1) Primer design
[0033] According to the sequence (Soltu.DM.10G025990.1) (Soltu.DM.10G025990.1) (such as sequence table SEQ No.2) of the StABL1 gene published in the potato genome database (http: / / spuddb.uga.edu / ) in the present invention, design primers to amplify the gene The full-length CDS sequence, the primer sequence is as follows:
[0034] StABL1 F (5'-ATGGGATCTCAGGGTGGTG-3')
[0035] StABL1 R (5'-TTAGACGGGCGCGGAGCTTGTTCTG-3')
[0036] In addition, quantitative primers for StABL1 were designed, and the primer sequences are as follows:
[0037] qStABL1F(5'-GAACTGGAGAACAAGGTTTCAC-3')
[0038] qStABL1R(5'-GACATAACGAACACTACGCATC-3')
[0039] (2) RNA extraction
[0040] The leaf samples of the cultivar Epotas 3 (E3) were taken, ground into powder in liquid nitrogen, and RNA was extracted according to the ...
Embodiment 3
[0084] This embodiment provides the application of potato StABL1 gene, specifically as follows:
[0085] Using E3 as the genetic material, the transformed excess strains were OE-StABL1 (10, 13); using E109 as the genetic material, the transformed excess strains were OE-StABL1 (1, 2). In the tuber experiment in vitro, we transferred the single-segment excess lines OE-StABL1 (10, 13) and E3 into MS solid medium containing 8% sucrose, supplemented with 0.2% activated carbon, and placed in a short Sunlight growth chamber culture. From the fourth week, the tuber formation was recorded every week. In the in vivo tuber experiment, the excess strain OE-StABL1 (10, 13), the control E3, the excess strain OE-StABL1 (1, 2) and the control E109 were planted in the net room, and cultivated in long-day light for about 4 weeks (10-leaf stage), the excess strain OE-StABL1 (10, 13) and the control E3 were transferred to short-day light, and the phenotype was observed every 5 days. The excess ...
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