TNFR1 gene recombinant adenovirus and construction thereof

Abstract

The invention discloses a TNFR1 gene recombinant adenovirus. The adenovirus contains siRNA expressed by an interference TNFR1 gene of a nucleotide sequence shown in SEQ ID No.1, the siRNA is connected to the place below a U6 promoter of shuttle plasmid pHBAd-U6-GFP to prepare an adenovirus shuttle plasmid, and then the adenovirus shuttle plasmid and a skeleton plasmid pHBAd-BHG are subjected to cotransfection 293 cells to obtain adenovirus Ad-TNFR1 shRNA. The TNFR1 gene recombinant adenoviru is used for blocking or reducing TNFR1 expression and blocking a biological effect produced through TNF in a new way, so that tool medicine is designed to explore the effect of TNFR1 in hyperalgesia generation and the intracellular action mechanism, and medicine for preventing inflammatory factors from activating a receptor is designed to weaken the hyperalgesia effect caused after receptor activation.

Description

technical field

[0001] The invention belongs to the technical field of genetic bioengineering and relates to the construction of an adenovirus, in particular to a recombinant adenovirus that interferes with the expression of TNFR1. Background technique

[0002] NMDA receptors are an important class of excitatory amino acid receptors in the central nervous system. They are ionotropic receptors and play an important role in synaptic plasticity and excitotoxicity.

[0003] NMDA receptors are heterotetramers composed of NR1, NR2, and NR3 subunits, each of which is distributed differently in the central nervous system. It is generally believed that NR1 is an essential subunit of NMDA receptors, distributed in large quantities in the brain and spinal cord, and is necessary for the realization of its channel function. NMDA receptors not only play an important physiological role in the development of the nervous system, but also play a key role in the formation of neuronal circuits...

Examples

Embodiment 1

[0022] Design the siRNA sequence that interferes with the expression of TNFR1, specifically: 5'-attgttactaagcccctaact-3'.

[0023] The shRNA expression sequence containing the above siRNA was artificially synthesized, the sequence was connected to the sense strand and the antisense strand of the above siRNA through a loop of 7 bases, and BamHI and EcoRI restriction sites were respectively introduced at both ends of the sequence.

[0024] Topstrand (62bp):

[0025] 5'-AATTCGattgttactaagcccctaactTGTGCTTagttaggggcttagtaacaatTTTTTTg-3';

[0026] Bottomstrand (62bp):

[0027] 5'-GATCCAAAAAAAattgttactaagcccctaactAAGCACAagttaggggcttagtaacaatCg-3'.

[0028] The above-mentioned complementation utilizes 3' and 5' single-strand annealing to obtain the double-strand expression template annealing product of the corresponding target fragment shRNA. The annealing procedure is:

[0029] System: 20μl;

[0030] 10×Buffer2μl;

[0031] 100mM Tris-Cl pH7.5;

[0032] 1M NaCl;

[0033] 10mM ...

Embodiment 2

[0052] Take 2ml of the adenovirus shuttle plasmid bacterial solution in the logarithmic growth phase prepared in Example 1, add it to 100ml LB medium containing 100μg / ml Amp, shake the bacteria overnight at 37°C and 300rpm, and extract the plasmid with the Kangwei Century Zhongli Plasmid Kit .

[0053] The day before transfection, 293 cells were inoculated in 60 mm culture dishes, the medium was DMEM+10% Hyclon fetal bovine serum, and placed at 37°C with 5% CO 2 cultured overnight in an incubator.

[0054] When the cells grow to 70-80% of the bottom area, take the recombinant adenovirus vector plasmid TNFR1shRNA and the backbone plasmid pHBAd-BHG, and use Lipofiter TM Lipofectamine (Hanbio) transfection reagent was used for transfection.

[0055] The specific steps are:

[0056] a. Replace the complete medium 2 hours before transfection. Take 2 μg of recombinant adenovirus vector plasmid TNFR1shRNA and 4 μg of backbone plasmid pHBAd-BHG, dilute them with 300 μl of DMEM me...

Embodiment 3

[0066] At a density of 2×10 5 Plant the MEF cell line into a 6-well plate. After the cells grow to 60% confluence, they are infected with Ad-GFP and Ad-TNFR1shRNA adenovirus respectively, at 37°C and 5% CO 2 Cultivate in the incubator for 2 hours, replace the culture medium, and observe the fluorescent expression of GFP under a fluorescent microscope after culturing for 36 hours. The results are as follows: image 3 shown.

[0067] Collect the cells, wash them 3 times with PBS, scrape the cells with a scraper, transfer them into EP tubes, centrifuge at 1000rpm for 3 minutes, discard the supernatant, freeze the cell pellets with liquid nitrogen and store them in a -8°C refrigerator. Take out the cells from the -80°C refrigerator, add 500 μl RIPA Complete Lysis Solution, lyse on ice for 2 hours, centrifuge at 12,000 rpm for 30 minutes, collect the supernatant, and discard the precipitate. The protein content in the supernatant samples was determined by the BCA method, and the ...

technical field

[0001] The invention belongs to the technical field of genetic bioengineering and relates to the construction of an adenovirus, in particular to a recombinant adenovirus that interferes with the expression of TNFR1. Background technique

[0002] NMDA receptors are an important class of excitatory amino acid receptors in the central nervous system. They are ionotropic receptors and play an important role in synaptic plasticity and excitotoxicity.

[0003] NMDA receptors are heterotetramers composed of NR1, NR2, and NR3 subunits, each of which is distributed differently in the central nervous system. It is generally believed that NR1 is an essential subunit of NMDA receptors, distributed in large quantities in the brain and spinal cord, and is necessary for the realization of its channel function. NMDA receptors not only play an important physiological role in the development of the nervous system, but also play a key role in the formation of neuronal circuits...

Examples

Embodiment 1

[0022] Design the siRNA sequence that interferes with the expression of TNFR1, specifically: 5'-attgttactaagcccctaact-3'.

[0023] The shRNA expression sequence containing the above siRNA was artificially synthesized, the sequence was connected to the sense strand and the antisense strand of the above siRNA through a loop of 7 bases, and BamHI and EcoRI restriction sites were respectively introduced at both ends of the sequence.

[0024] Topstrand (62bp):

[0025] 5'-AATTCGattgttactaagcccctaactTGTGCTTagttaggggcttagtaacaatTTTTTTg-3';

[0026] Bottomstrand (62bp):

[0027] 5'-GATCCAAAAAAAattgttactaagcccctaactAAGCACAagttaggggcttagtaacaatCg-3'.

[0028] The above-mentioned complementation utilizes 3' and 5' single-strand annealing to obtain the double-strand expression template annealing product of the corresponding target fragment shRNA. The annealing procedure is:

[0029] System: 20μl;

[0030] 10×Buffer2μl;

[0031] 100mM Tris-Cl pH7.5;

[0032] 1M NaCl;

[0033] 10mM ...

Embodiment 2

[0052] Take 2ml of the adenovirus shuttle plasmid bacterial solution in the logarithmic growth phase prepared in Example 1, add it to 100ml LB medium containing 100μg / ml Amp, shake the bacteria overnight at 37°C and 300rpm, and extract the plasmid with the Kangwei Century Zhongli Plasmid Kit .

[0053] The day before transfection, 293 cells were inoculated in 60 mm culture dishes, the medium was DMEM+10% Hyclon fetal bovine serum, and placed at 37°C with 5% CO 2 cultured overnight in an incubator.

[0054] When the cells grow to 70-80% of the bottom area, take the recombinant adenovirus vector plasmid TNFR1shRNA and the backbone plasmid pHBAd-BHG, and use Lipofiter TM Lipofectamine (Hanbio) transfection reagent was used for transfection.

[0055] The specific steps are:

[0056] a. Replace the complete medium 2 hours before transfection. Take 2 μg of recombinant adenovirus vector plasmid TNFR1shRNA and 4 μg of backbone plasmid pHBAd-BHG, dilute them with 300 μl of DMEM me...

Embodiment 3

[0066] At a density of 2×10 5 Plant the MEF cell line into a 6-well plate. After the cells grow to 60% confluence, they are infected with Ad-GFP and Ad-TNFR1shRNA adenovirus respectively, at 37°C and 5% CO 2 Cultivate in the incubator for 2 hours, replace the culture medium, and observe the fluorescent expression of GFP under a fluorescent microscope after culturing for 36 hours. The results are as follows: image 3 shown.

[0067] Collect the cells, wash them 3 times with PBS, scrape the cells with a scraper, transfer them into EP tubes, centrifuge at 1000rpm for 3 minutes, discard the supernatant, freeze the cell pellets with liquid nitrogen and store them in a -8°C refrigerator. Take out the cells from the -80°C refrigerator, add 500 μl RIPA Complete Lysis Solution, lyse on ice for 2 hours, centrifuge at 12,000 rpm for 30 minutes, collect the supernatant, and discard the precipitate. The protein content in the supernatant samples was determined by the BCA method, and the ...

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