Novel multifunctional dual-luciferase reporter gene plasmid

A luciferase gene and dual luciferase technology, which is applied in the fields of molecular biology and genetic engineering, can solve the problems of inability to use and limit the application range of miRNA target identification plasmids, so as to reduce experimental errors, facilitate extraction, and improve experiments. The effect of efficiency

Inactive Publication Date: 2018-12-18
SUN YAT SEN UNIV
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AI Technical Summary

Problems solved by technology

However, the fixed promoter in pmirGLO can only express the promoter gene in most mammalian cells, which greatly limits the scope of application of this miRNA target identification plasmid, and pmirGLO only introduces polyclonal expression downstream of firefly luciferase site, the plasmid can only be used for miRNA target identification, but not for other dual-luciferase reporter gene detection studies such as promoter activity regulation identification

Method used

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  • Novel multifunctional dual-luciferase reporter gene plasmid
  • Novel multifunctional dual-luciferase reporter gene plasmid
  • Novel multifunctional dual-luciferase reporter gene plasmid

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Embodiment

[0029] 1. Plasmid Construction

[0030] Material: High Fidelity Enzyme HS (Premix) (Takara, Japan), DNA Ladder (Dongsheng, China), Agarose Gel DNA Recovery Kit (Magen, China), restriction enzyme EcoRI (NEB, UK), Plasmid Mini Kit I (OMEGA, P / N: D6942-01)

[0031] The specific sequences of the designed primers are shown in Table 1

[0032] Table 1. Primer sequences

[0033]

[0034] 1.1 Deletion of the PGK promoter in mutant pmirGLO

[0035] Steps: ① Design and synthesize primers pmiRGLO-EcoRI-FseIF and pmiRGLO-EcoRI-AscIR according to the pmirGLO vector sequence: use the high-fidelity enzyme Premix to clone the pmirGLO vector DNA of the human phosphoglycerate kinase PGK promoter sequence from the pmirGLO vector; ②PCR After the reaction, the product was separated by 1% agarose gel electrophoresis, and the target DNA band was quickly excised under ultraviolet light with reference to the 1kb DNA Ladder (estimated product size: 6385bp), and the target DNA was recovered usi...

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Abstract

The invention discloses a novel multifunctional dual-luciferase reporter gene plasmid. The plasmid contains a luc firefly luciferase gene, a Rluc renilla luciferase gene, a SV40 poly(A) termination signal part and two independent multiple cloning sites, wherein the two independent multiple cloning sites are located on the upstream and the downstream of a luc firefly luciferase gene coder frame respectively. The dual-luciferase reporter gene plasmid containing detection gene and reference gene is successfully constructed, not only can the detection gene be transferred into a subject cell conveniently, but also the reference gene can be taken in correspondingly, the complexity of experiment operation and experiment errors are greatly reduced, the plasmid has the multiple cloning sites at thetwo ends of the firefly luciferase gene, the multiple cloning site located on the upstream of firefly luciferase can introduce a promoter sequence which can be used for genetic transcription adjustment, control and detection, and the multiple cloning site located on the downstream of the firefly luciferase can introduce a 3'UTR sequence which can be used for miRNA target identification, so that switching of different application of the same plasmid is achieved.

Description

technical field [0001] The invention relates to the fields of molecular biology and genetic engineering, in particular to a novel multifunctional double luciferase reporter gene plasmid. Background technique [0002] Luciferase is a general term for a class of enzymes that catalyze the oxidation and luminescence of luciferin or adipose fluorescein in organisms. Luciferase can catalyze luciferin to form oxidized luciferin. During the luciferin oxidation process, bioluminescence is emitted, and the intensity of bioluminescence can be detected and recorded by a chemiluminescence instrument. The luciferase reporter gene system is a reporter system that uses luciferin as a substrate to detect luciferase activity. It can detect gene expression extremely sensitively and efficiently, and is an important detection method for detecting gene transcription or translation regulation. [0003] When using luciferase to quantitatively detect gene expression, the second reporter gene is usu...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/63C12N15/52C12N15/66
CPCC12N9/0069C12N15/63C12N15/66C12Y113/12005C12Y113/12007
Inventor 左洪亮徐晓鹏李朝政翁少萍何建国
Owner SUN YAT SEN UNIV
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