MYB transcription inhibition factor LrMYB3 related to lycium ruthenicum anthocyanin synthesis and application thereof

A technology of transcription repressor and anthocyanin, which is applied in the field of genetic engineering and can solve problems such as unreported

Active Publication Date: 2021-08-27
WOLFBERRY SCI INST NINGXIA ACAD OF AGRI & FORESTRY SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

MYB transcription factors play an important role in the regulation of anthocyanin metabolism. Although some research results have reported several MYB transcription factors

Method used

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  • MYB transcription inhibition factor LrMYB3 related to lycium ruthenicum anthocyanin synthesis and application thereof
  • MYB transcription inhibition factor LrMYB3 related to lycium ruthenicum anthocyanin synthesis and application thereof
  • MYB transcription inhibition factor LrMYB3 related to lycium ruthenicum anthocyanin synthesis and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0062] For the extraction of DNA and RNA, refer to the kit instructions, and operate in a conventional manner.

[0063] Synthesis of single-stranded cDNA: Using the total RNA of Lycium barbarum fruit as a template, the single-stranded cDNA was synthesized using the experimental steps given by Takara's PrimeScriptTMRT reagent Kit with gDNA Eraser (Perfect Real Time).

[0064] Cloning of LrMYB3 gene: See Table 2 for the sequences of the amplification primers. The primers were diluted to 10 μM, and the obtained cDNA was used as a template for PCR amplification reaction. The reaction system is shown in Table 3 below.

[0065] Table 2

[0066]

[0067]

[0068] table 3

[0069]

[0070] After the amplification is completed, take out the PCR product and perform 1% agarose gel electrophoresis detection. After electrophoresis for about 7 minutes, observe it under a UV gel imager. If the target band is single and the size is correct, cut out the gel piece and place it in the ...

Embodiment 2

[0086] The open reading frame and deduced amino acid sequence of the LrMYB3 transcription factor were searched through the ORF Finder (https: / / www.ncbi.nlm.nih.gov / orffinder / ) online search tool on NCBI. The online software ProtParam (http: / / web.expasy.org / protparam / ) was used to predict the amino acid composition, protein molecular weight, theoretical isoelectric point and stability of transcription factors. The hydrophobicity and charge distribution of proteins were analyzed using the online software ProtScale (https: / / web.expasy.org / protscale / ). The transmembrane domain of LrMYB3 protein was analyzed using TMHMM 2.0 (http: / / www.cbs.dtu.dk / services / TMHMM) software. The signal peptide of the protein was predicted by Cell-PLoc2.0 (http: / / www.cbs.dtu.dk / services / Sign alP). Use Wolf Psort (https: / / www.genscript.com / wolf-psort.html) and online software (https: / / www.csbio.sjtu.edu.cn / bioinf / Cell-PLoc-2 / ) to predict Subcellular localization of proteins. Use SOPMA (https: / / npsa-p...

Embodiment 3

[0163] Construction of Plant Overexpression Recombinant Vector

[0164] Cloning of target gene homologous recombination fragment:

[0165] Using the cDNA solution obtained in the steps of the above examples as a template, the corresponding primers in Table 12 were used to amplify the homologous recombination fragment of the plant overexpression vector. The amplification system, detection and recovery of PCR products are the same as those in the above examples.

[0166] Table 12

[0167]

[0168] Carrier digestion reaction

[0169] The vector pCM1307 was double-digested with two restriction enzymes XbaI and KpnI; the vector pZYB9-pEAQ-HT was double-digested with two restriction enzymes SmaI and StuI. The enzyme digestion system and product recovery are the same as those in the above-mentioned examples.

[0170] Homologous recombination connection fragments and vectors, Escherichia coli DH5α transformation, bacterial liquid PCR identification and plasmid extraction are the...

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Abstract

The invention discloses an MYB transcription inhibition factor LrMYB3 related to lycium ruthenicum anthocyanin synthesis and application thereof, and belongs to the technical field of gene engineering. According to transcriptome data of lycium ruthenicum, the MYB transcription inhibition factor LrMYB3 participating in anthocyanin synthesis is screened and cloned according to annotation results and expression quantity differences of MYB transcription factors, and belongs to a R2R3 type MYB transcription factor. Multiple sequence alignment and evolutionary tree analysis show that the transcription inhibition factor belongs to a FaMYB1-like transcription inhibition factor. QRT-PCR analysis shows that: the LrMYB3 is expressed in each tissue of the lycium ruthenicum, and the expression level is gradually increased along with ripening of the lycium ruthenicum. Subcellular localization and transcriptional activity detection experiments show that the LrMYB3 is a transcription factor which is localized in a cell nucleus and has no activation function.

Description

technical field [0001] The invention relates to the technical field of genetic engineering, and more specifically relates to a MYB transcription inhibitor LrMYB3 related to anthocyanin synthesis of Lycium barbarum black fruit and its application. Background technique [0002] Lycium ruthenicum Murry (Lycium ruthenicum Murry.) belongs to the Solanaceae (Solanaceae) Lycium genus deciduous thorny shrubs. It is rich in nutrition and has both medicine and food. It has attracted widespread attention because of its rich anthocyanins. Anthocyanins have strong antioxidant activity, which can not only help plants resist stressful environments, but also have great benefits in promoting human health. [0003] Transcription factors, also known as trans-acting factors, usually refer to a class of proteins encoded by genes, which can specifically bind to relevant cis-acting elements in the gene promoter region to activate or inhibit gene expression, thereby increasing the plant's response ...

Claims

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Application Information

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IPC IPC(8): C07K14/415C12N15/29C12N15/82A01H5/00A01H6/82
CPCC07K14/415C12N15/825
Inventor 曹有龙唐琳樊云芳秦欢张曦燕李婷婷陈晓军赵建华李彦龙王亚军张波
Owner WOLFBERRY SCI INST NINGXIA ACAD OF AGRI & FORESTRY SCI
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