Method for improving content of 5-methyltetrahydrofolate by gene knockout
A methyltetrahydrofolate and gene knockout technology, applied in the fields of genetic engineering and molecular biology, can solve folic acid deficiency, changes in DNA methylation level and pattern, accelerate the development of colon cancer and prostate cancer, and precancerous lesions, etc. problem, achieve the effect of increasing folic acid content and alleviating hidden hunger
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Embodiment 1
[0027] Example 1 Corn ZmGFT1 Construction of gene knockout vector and acquisition and identification of transgenic plants
[0028] (1) The leaves of maize inbred line C01 were collected, the total RNA of maize was extracted by Trizol method, and the cDNA of maize was obtained with RevertAid First Strand cDNA Synthesis Kit (Thermo). Using maize cDNA as a template, Primer1 (SEQ ID NO.5) / Primer2 (SEQ ID NO.6) as amplification primers, the CDS full-length of the GRMZM2G124863 gene was amplified ( figure 1 A).
[0029] (2) Referring to the results of the sequencing sequence, design two target sites in the genomic region corresponding to the GFT1 exon ( figure 1 T1 and T2 of B, design website: http: / / cas9.cbi.pku.edu.cn / index.jsp), these two targets have common characteristics in the genome, NGG at the 3' end (N is A , T, C, G any base), the sequence is SEQ ID NO.3 and SEQ ID NO.4.
[0030] (3) Referring to the method of gene knockout vector construction (Li CX, Liu CL et al.,...
Embodiment 2
[0040] Example 2 ZmGFT1 Detection of gene knockout maize transcription level
[0041] Will ZmGFT1 The negative transgenic T0 generation plants with gene knockout and no CRISPR / Cas9 recombinant plasmid were selfed to obtain stable genetic ZmGFT1 Gene knockout T1 generation line. Will ZmGFT1 The gene knockout T1 generation plants were selfed, and the grain materials 25 days after pollination were taken, frozen in liquid nitrogen, and ground into powder, and total RNA was extracted using a total RNA extraction kit (purchased from Beijing Yuanpinghao Biotechnology Co., Ltd.). RevertAid First Strand cDNA Synthesis Kit (Thermo) was used to obtain cDNA. Transgenic plants were detected by qRT-PCR detection kit (purchased from Beijing Quanshijin Biotechnology Co., Ltd.) ZmGFT1 gene transcription levels. PCR reaction system: DNA template 1 μl, Primer9 (SEQ ID NO.13) 0.4 μl, Primer10 (SEQ ID NO.14) 0.4 μl, Dye II 0.4 μl, 2X Buffer 10 μl, ddH 2 O 7.8 μl; PCR amplification program: ...
Embodiment 3
[0042] Example 3 ZmGFT1 Determination of Folic Acid Content in Gene Knockout Maize
[0043] Utilize high performance liquid chromatography mass spectrometry to measure described in embodiment 2 ZmGFT1 Folic acid content in leaves and grains of transgenic maize (including monoglutamic acid-tailed 5-methyltetrahydrofolate, diglutamic acid-tailed 5-methyltetrahydrofolate, triple-glutamic acid-tailed 5-methyltetrahydrofolate). Organs tested included fresh leaves 70 days after planting and fresh seeds 25 days after pollination.
[0044] The result is as Figure 6-8 as shown, ZmGFT1 The content of 5-methyltetrahydrofolate, the main form of folic acid, in the leaves and grains of transgenic maize was significantly higher than that in the control (wild type). In fresh leaves planted for 70 days, the gene knockout mutants had about 2.01-2.23 times more monoglutamic tail 5-methyltetrahydrofolate and 2.23 times more diglutamic tail 5-methyltetrahydrofolate than the wild type. Increa...
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