Novel watermelon sugar transporter as well as coding gene ClVST1 and application thereof
A technology of transgenic plants and proteins, applied in application, genetic engineering, plant genetic improvement, etc., can solve the problems of low selection efficiency, high cost, and heavy workload.
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Embodiment 1
[0068] This example is used to illustrate the discovery, cloning and localization of a novel watermelon sugar transporter and its encoding gene CLVST1.
[0069] 1. The discovery of a novel sugar transporter in watermelon and its encoding gene CLVST1
[0070] "By using the ultra-high-density SNP genetic map and 326 natural population materials, the fine mapping and association analysis of the sugar content of watermelon fruit were completed, and the watermelon database was used to retrieve and compare the related gene sequences of other species, and one was obtained from the watermelon variety 97103. The new protein is named as watermelon novel sugar transporter, and its sequence is shown in sequence 1 in the sequence table (consisting of 470 amino acid residues). The gene encoding the watermelon novel sugar transporter is named CLVST1 gene, and its cDNA The open reading frame is shown in Sequence 2 in the Sequence Listing (consisting of 1413 nucleotides).
[0071] 2. Cloning ...
Embodiment 2
[0082] This example is used to illustrate the acquisition of CRISPR knockout CLVST1 plants.
[0083] 1. Construction of CRISPR-ClVST1 knockout vector
[0084] 1. pCBC-DT1T2 (Xing, H.L.#, Dong, L.#, Wang, Z.P., Zhang, H.Y., Han, C.Y., Liu, B., Wang, X.C., and Chen, Q.J. *(2014). A CRISPR / Cas9 toolkit for multiplex genome editing in plants. BMC Plant Biol 14, 327.) PCR amplification as template. The sequence composition of the four primers is as follows.
[0085] Sequence composition of DT1-BsF-ClVST1:
[0086] 5'-ATATATGGTCTCGATTGAAATCAAAACCACTCCCTTACTGGGTT-3';
[0087] Sequence composition of DT1-F0-ClVST1:
[0088] 5'-TGAAATCAAACCACTCCCTTACTGGGTTTTAGAGCTAGAAATAGC-3';
[0089] Sequence composition of DT2-R0--ClVST1: 5'-AACGGTCGAGGCGAGGCCGGCGCAATCTCTTAGTCGACTCTAC-3';
[0090] Sequence composition of DT2-BsR--ClVST1:
[0091] 5'-ATTATTGGTCTCGAAAC GGTCGGAGGCGAGGCCGGCGCAA-3'.
[0092] 20μL PCR reaction system: pCBC-DT1T2 template, 10×Buffer 2μL, 10mmol / L dNTPs 2μL, MgSO 4...
Embodiment 3
[0137] This example is used to illustrate the disease resistance response of gene knockout homozygous lines to bacterial fruit spot.
[0138] 1. Disease resistance analysis of watermelon gene knockout homozygous lines
[0139] The CLVST1 gene knockout homozygous strain VST1-CRISPR (three groups, average value for each group) and receptor 97103 (three groups, average value for each group) obtained in Example 2 were primed respectively. The vermiculite after high temperature sterilization is used as the matrix, and the vermiculite is covered after sowing, and the film is covered with heat preservation and moisturizing. Referring to the identification method of artificial inoculation of watermelon bacterial fruit spot reported by Zhao Tingchang et al., the pathogenicity of the strain was determined by spray inoculation. The virulence of M. melon fruit spot mutant strain, wild type strain and complementary strain (Ren Zhengguang, Lin Min, Jiang Wenjun, et al.. quorum sensing syst...
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