Application of isatis indigotica fort IiAP2/ERF049 gene to regulating and controlling synthesis of lignan compound
A technology of woad and gene, applied in the field of genetic engineering, to achieve the effect of reducing pollution, great application prospects, and increasing content
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Embodiment 1
[0047] Embodiment 1: Screening of Isatis indigo AP2 / ERF transcription factor
[0048] Arabidopsis thaliana AP2 / ERF transcription factors were downloaded from the Arabidopsis database (DATF, http: / / datf.cbi.pku.edu.cn / ) and the Chinese cabbage database (http: / / brassicadb.org / brad / ) respectively 159 (Arabidopsisthaliana AP2 / ERFs, AtAP2 / ERFs) and 321 Chinese cabbage AP2 / ERF transcription factors (Chinese cabbageAP2 / ERFs, BraAP2 / ERFs), according to their amino acid sequences to establish the Brassicaceae AP2 / ERF database. Use the TBLASTN algorithm to compare this database with the Isatis indigo transcriptome database (the e-value value is set to 10 -5 ), identify and extract genes homologous to Brassicaceae AP2 / ERF in the Isatis indigo transcriptome database as Isatis indigo AP2 / ERF candidate genes.
[0049] Bioinformatics software Vector NTI 11.5 and MEGA 5.05 were used to analyze the nucleotide sequence of the Isatis indigo AP2 / ERF candidate gene obtained above, extract the ope...
Embodiment 2
[0052] Embodiment 2: the cloning of woad IiAP2 / ERF049 gene
[0053] 1. Isatis indica DNA and total RNA extraction
[0054] Take about 100 mg of Isatis indigo sterile seedlings, grind them into powder quickly in liquid nitrogen, and use the CTAB method to extract Isatis indigo DNA; take another about 100 mg of Isatis indigo sterile seedlings, quickly grind them into powder in liquid nitrogen, add the pre-installed plant tissue cracking solution in a 1.5ml centrifuge tube, shake and mix well, and then follow the TIANGEN TRNzol-A + Total RNA was extracted from Isatis indica according to the instructions of the total RNA extraction kit. Use 1% agarose gel electrophoresis to identify the quality of DNA and total RNA, and use a Nano drop 2000C spectrophotometer (Thermo Scientific, San Jose, California, USA) to detect the purity and concentration of DNA and total RNA;
[0055] 2. Isatis indigo IiAP2 / ERF049 gene cloning
[0056] Using 1 μg of the extracted total RNA as a template, ...
Embodiment 3
[0064] Example 3: Analysis of the subcellular localization of the woad IiAP2 / ERF049 gene
[0065] According to the content of the bioinformatics analysis in Example 2, the IiAP2 / ERF049 gene is an AP2 / ERF transcription factor with an AP2 domain. In order to further verify the nature of IiAP2 / ERF049 gene as a transcription factor, we constructed the subcellular localization vector of IiAP2 / ERF049 gene, and confirmed that IiAP2 / ERF049 is localized in the nucleus by transforming rice protoplasts, which conforms to the characteristics of transcription factors.
[0066] 1. Construction of subcellular localization vector
[0067] In this embodiment, according to the pCAMBIA1301-GFP vector sequence and the IiAP2 / ERF049 gene ORF region sequence, design primers with restriction sites, wherein the forward primer contains the Nco I restriction site (5'-AA CCATGG GAATGGTGAGCTTAAGAAGG-3', SEQ ID NO: 6), the reverse primer contains a Spe I restriction site (5'-GG ACTAGT GGTAGAAAGTGTACTGA...
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