A kind of chicken mda5 gene promoter and application thereof

A promoter and promoter sequence technology, applied in the field of genetic engineering, can solve the problems of unclear regulatory mechanism of MDA5 and unreported research, and achieve the effect of convenient verification, prediction and screening

Active Publication Date: 2018-01-19
GUANGXI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there are many studies on the regulation mechanism of RIG-I, but the regulation mechanism of MDA5 is still unclear, and the study on the promoter of chicken MDA5 gene has not been reported.

Method used

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  • A kind of chicken mda5 gene promoter and application thereof
  • A kind of chicken mda5 gene promoter and application thereof
  • A kind of chicken mda5 gene promoter and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Embodiment 1: chicken melanoma differentiation-associated gene 5 (MDA5) promoter fragment and corresponding acquisition

[0031] NCBI database (http: / / www.ncbi.nlm.nih.gov) searched the upstream regulatory sequence of chicken melanoma differentiation-related gene MDA5, predicted the approximate region of MDA5 promoter, and used this sequence as the research object. Design primers (the primer sequence is shown in Table 1), and use the white chicken genomic DNA as a template to amplify the promoter region of MDA5 by PCR. The amplified products are identified by 1% agarose gel electrophoresis and purified and recovered with Tiangen recovery kit , the fragment was connected to the pMD19-T (Takara) vector, and sent to the handsome company for sequencing. The obtained promoter sequence is shown in SEQ ID NO:3.

[0032] Primer name

Embodiment 2

[0033] Example 2: Construction of chicken melanoma differentiation-associated gene 5 (MDA5) promoter transfection vector

[0034] Using the MDA5 promoter connected to the pMD19-T vector as a template, primers were designed for PCR amplification, and two Dicer sites, PciⅠ and BamHI, were introduced. The sequences of the primers are shown in Table 2. The amplified product was identified by 1% agarose gel electrophoresis and purified and recovered with the Tiangen recovery kit, then connected to the pEASY-T1 vector with the full-type gold pEASY-T1 Cloning Kit kit, and sent to Yingjun Company sequencing. After sequence comparison, select the samples with correct sequencing for future use.

[0035] Table 2 Amplification primers introducing PciⅠ and BamHI restriction sites

[0036]

[0037] Use restriction endonucleases PciⅠ and BamHI (both purchased from NEB Company) to double-digest the vector pDsRed1-N1 plasmid (Clontech) and the promoter fragment connected to pEASY-T1 respe...

Embodiment 3

[0058] Example 3: Cell Transfection of Recombinant Plasmids

[0059] In this study, chicken embryonic fibroblasts (DF-1) were adherent cells, which were cultured by adherent cell culture method. The cells are passaged in culture dishes or well plates, cultured in a 37°C incubator with a carbon dioxide concentration of 5%, and the growth status of the cells, such as cell shape and density, is observed through a microscope. Under normal circumstances, subculture once every three days. The cell culture medium is DMEM high-glucose medium containing 10% fetal bovine serum and 0.01% penicillin-streptomycin solution.

[0060] Prior to cell transfection, transfer the cells into a 24-well plate to reach a density of 70-80% within 24 hours. Cell transfection was carried out by liposome method at about 24 hours. The liposome used was Lipofectamine® LTX & PLUS Reagent (Invitrogen), and the specific operation was carried out strictly according to the instructions.

[0061] About 36 hou...

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PUM

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Abstract

The invention discloses a chicken MDA5 gene promoter, the sequence of which is shown as SEQ ID NO: 3 in the sequence table, and the length of the MDA5 gene promoter sequence is 2487bp. The invention also discloses the cloning method and application of the MDA5 gene promoter. The invention verifies the ability of the chicken MDA5 gene promoter to initiate gene expression in cells, verifies the regulation and control of the promoter expression by different stimuli, and brings deeper cognition for the expression regulation of the MDA5 gene.

Description

technical field [0001] The invention belongs to the technical field of genetic engineering, and in particular relates to the isolation, identification and application of a promoter region of chicken natural immunity-related gene MDA5. Background technique [0002] Innate immunity, also known as nonspecific immunity or innate immunity, mainly realizes the removal and killing of pathogens through natural immune molecules and cells. Through the recognition of pathogens, host cells activate a series of downstream cascade reactions, which eventually lead to the production of type I interferons, pro-inflammatory cytokines, chemokines, etc., thereby inhibiting the replication of pathogens, resisting infection and clearing pathogens. The recognition of innate immunity to pathogens depends on pathogen molecular pattern recognition receptors (PRR). [0003] Melanoma Differentiation-Associated protein 5 (MDA5, also known as Helicard, IFIH1) is a pathogen molecular pattern recognition ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N15/113C12N15/10C12N15/55C12N15/85
Inventor 陆阳清张文馨陈东阳左二伟卢克焕
Owner GUANGXI UNIV
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