A kind of ku70 protein mutant with the function of inhibiting tumor cell proliferation, gene and application
A technology for tumor cell proliferation and protein mutants, applied in the field of genes and applications, Ku70 protein mutants, can solve the problems of dose dependence, patient sensitivity, and serious side effects
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Embodiment 1
[0018] Example 1: MU4 protein expression vector pbicep-n-flag-mu4 cloning construction
[0019] The lack of anti-transcripts are designed according to the gene full sequence (NM_001288977) of the Ku70 protein, and a variant Ku70 protein for constructing a deletion C-terminal 37 amino acids, and the sequence of mutant primers is shown in Table 1.
[0020] Table 1 mutation primer
[0021]
[0022] The PbiceP-N-Flag-Ku70 plasmid preserved in the laboratory is a full length of the wild type in the multi-clon site of commercial plasmid pBiceP-CMV-3 (purchased from Sigma). U70 Gene sequence (granular map figure 1 ).
[0023] The PbiceP-N-Flag-Ku70 plasmid was a template, and the PbiceP-N-Flag-MU4 plasmid DNA fragment was obtained by mutation PCR method, and the PCR reaction system was shown in Table 2.
[0024] Table 2 PCR amplification system
[0025] Template DNA 1μL Upstream primer (10μm) 1μL Downstream primer (10μm) 1μL DREAMTAQ PCR MASTER MIX (2 ×) 25μL ...
Embodiment 2
[0032] Example 2: Mu4 protein on SHKU70 / HELA cell proliferation inhibitory activity
[0033] (1) Screening Shku70 / HeLA cells
[0034] The Ku70 shRNA plasmid was transferred to HeLa cells using liposome transfection. Ku70ShRNA plasmids from Jikai Company, plasmid map (GV248 plasmid) figure 2 As shown, the coding sequence of the Ku70 Shrna is inserted into the polyclon position (as shown in SEQ ID NO 5). The plasmid transfected into the cells, which expressed ShRNA targeted to Ku70 mRNA, thereby inhibiting the expression of Ku70, reducing the Ku70 protein level within the cell.
[0035] After 24 hours of transfection, 1 μg / ml of puromycin was added to the medium to screen the Hele cells which were integrated into the plasmid DNA in the genome. After screening for 1 month, a limited dilution method and monoclonal picking method were used to obtain SHKU70 / HELA cells expressed in endogenous Ku70.
[0036] (2) Liposome transfection method to shku70 / heLA cells into pBiceP-N-Fla...
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