Disease-resistant transgenic soybean event b5c9120-3 foreign insert fragment flanking sequence and its application

A technology of transgenic soybeans and flanking sequences, applied in the field of plant biology, can solve problems such as disease-resistant transgenic soybeans that have not yet been found

Active Publication Date: 2022-02-11
JILIN ACAD OF AGRI SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0005] According to the analysis of existing patents and documents, no articles or patent reports related to the flanking sequence of the exogenous insert fragment of the disease-resistant transgenic soybean event B5C9120-3 have been found so far

Method used

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  • Disease-resistant transgenic soybean event b5c9120-3 foreign insert fragment flanking sequence and its application
  • Disease-resistant transgenic soybean event b5c9120-3 foreign insert fragment flanking sequence and its application
  • Disease-resistant transgenic soybean event b5c9120-3 foreign insert fragment flanking sequence and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Example 1. Analysis of the insertion site of the exogenous fragment of the transgenic soybean event B5C9120-3

[0038] 1. Genomic DNA extraction of transgenic soybean B5C9120-3

[0039] (1) Genomic DNA extraction: Take 1-2 g of young soybean leaves, grind them into powder with liquid nitrogen, and put them into a 50 mL centrifuge tube. Add 5mL extract solution A (100mmol / L Tris-HCl, pH8.0, 0.35mol / L sorbitol, 5mmol / L EDTA, pH8.0, 1% 2-mercaptoethanol), 3.5mL extract solution B (50mmol / L L Tris-HCl, pH8.0, 4.0mol / LNaCl, 1.8% CTAB, 25mmol / L EDTA, pH8.0), 0.3mL 30% sodium lauroyl sarcosinate and 2% PVP-360, incubated at 55°C 60-90 minutes, shaking gently several times during the period. Take out the centrifuge tube, add an equal volume of chloroform:isoamyl alcohol (24:1), shake it upside down for 15 minutes, and then centrifuge at room temperature for 10 minutes (13000rpm). Aspirate the supernatant, add 2 / 3 volume of pre-cooled isopropanol mixed with 1 / 10 volume of sup...

Embodiment 2

[0044] Example 2. Analysis of the left and right border flanking sequences of the transgenic soybean event B5C9120-3 exogenous insert

[0045] According to the exogenous insertion sequence of the transgenic soybean event B5C9120-3 and the upstream and downstream sequences of the insertion site in the soybean reference genome, PCR detection primers were designed. B5C9120-3 insertion site upstream sequence amplification primers are B5C9120LB-F1 (5'-CGTGGCAGTTCCTGATTTGTTC-3') and B5C9120LB-R1: (5'-CTTTATGTTATGTGGGTAAGTCACCT-3'); B5C9120-3 insertion site downstream sequence amplification primers For B5C9120RB-F1: (5'-ACATACTTCCTCCCTCTTCAGC-3') and B5C9120RB-R 1 (5'-CATAGGCAGCACCGAATAACC-3').

[0046]Using the B5C9120-3 genomic DNA as a template, the above primers were used for PCR amplification. The PCR reaction system (25uL) is: 10×PCR buffer 2.5uL, 10mmol / L dNTPs 0.5uL, 5U / uL Taq enzyme 0.5uL, sample DNA 1.0uL, 10umol / L forward primer 0.5uL, 10umol / L reverse Primer 0.5uL, ddH ...

Embodiment 3

[0048] Example 3. Specific PCR detection of transgenic soybean event B5C9120-3

[0049] According to the left border flanking sequence (as shown in SEQ-2) and the right border flanking sequence (as shown in SEQ-3) of the exogenous insert fragment of the transgenic soybean event B5C9120-3, specific detection primers were designed respectively. In the left border flanking sequence-specific detection primer combination, one of the primers is a forward primer designed based on the 1-483 site sequence of SEQ-2, as shown in SEQ-4; the other primer is based on SEQ-2 No. 484- The reverse primer designed for the sequence at position 957 is shown in SEQ-5. In the right border flanking sequence-specific detection primer combination, one of the primers is a forward primer designed based on the sequence of the 1-326 positions of SEQ-3, as shown in SEQ-6; the other primer is based on the 327- The reverse primer designed for the sequence at position 945 is shown in SEQ-7.

[0050] The DNA ...

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Abstract

The invention provides a flanking sequence of a disease-resistant transgenic soybean event B5C9120‑3 exogenous insert fragment and an application thereof, belonging to the field of plant biotechnology. Specifically, it relates to a broad-spectrum anti-mosaic virus transgenic soybean event B5C9120‑3 exogenous insert fragment left and right border flanking sequences and its application. The left border flanking sequence of the transgenic soybean event B5C9120‑3 exogenous insert fragment disclosed by the present invention is shown in SEQ‑2, and the right border flanking sequence is shown in SEQ‑3. The flanking sequence of the exogenous insert fragment of the transgenic soybean event B5C9120‑3 disclosed in the present invention can be used as the target DNA sequence to establish a specific detection method for the transgenic event. The flanking sequence of the exogenous insert fragment and the detection method provided by the present invention are suitable for the specific detection of the transgenic soybean event including parents, derivative lines or varieties, and its products including plants, tissues, seeds and products.

Description

technical field [0001] The invention relates to the field of plant biotechnology, in particular to a broad-spectrum anti-mosaic virus transgenic soybean event B5C9120-3 exogenous insertion fragment flanking sequence and application thereof. Background technique [0002] Soybean mosaic virus (SMV), bean common mosaic virus (BCMV) and watermelon mosaic virus (WMV) all belong to the genus Potyvirus. Potyvirus Y (Potyvirus) is the largest genus of plant viruses, which can infect many plants such as Solanaceae, Chenopodiaceae, Fabaceae, Cucurbitaceae, etc., and cause serious yield loss. SMV is a major viral disease affecting soybean production, and it is also one of the most important diseases in major soybean producing areas in my country. SMV can generally cause a 10% to 35% reduction in soybean yield, and even cause large-scale extinction in severe years and regions (Yang et al. 2013, 2014; Ross 1983). In foreign countries, SMV strains are divided into G1-G7 according to the...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N15/11C12Q1/6895
CPCC12Q1/6895C12Q2600/13
Inventor 杨向东董英山杨静贺红利邢国杰牛陆郭东全钱雪燕姚瑶
Owner JILIN ACAD OF AGRI SCI
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