Ku70 protein mutant with tumor cell proliferation inhibition function, and gene and application thereof
A technology for tumor cell proliferation and protein mutants, applied in the field of genes and applications, Ku70 protein mutants, which can solve the problems of patient sensitivity, serious toxic and side effects, and dose dependence.
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Embodiment 1
[0018] Example 1: Mu4 protein expression vector pBICEP-N-Flag-Mu4 clone construction
[0019] Deletion mutation primers were designed according to the complete sequence of the Ku70 protein gene (NM_001288977) to construct a mutant Ku70 protein with a deletion of 37 amino acids at the C-terminal. The sequences of the mutation primers are shown in Table 1.
[0020] Table 1 Mutation Primers
[0021]
[0022] The pBICEP-N-Flag-Ku70 plasmid preserved in the laboratory, this plasmid is to insert wild-type full-length Ku70 between the multiple cloning site MIu I and BamH I of the commercialized plasmid pBICEP-CMV-3 (purchased from Sigma Company) Gene sequence (see plasmid map figure 1 ).
[0023] Using the pBICEP-N-Flag-Ku70 plasmid as a template, the DNA fragment of the pBICEP-N-Flag-Mu4 plasmid was obtained by mutation PCR. The PCR reaction system is shown in Table 2.
[0024] Table 2 PCR amplification system
[0025] template DNA 1μl Upstream primer (10μM) ...
Embodiment 2
[0032] Example 2: Detection of the inhibitory activity of Mu4 protein on the proliferation of ShKu70 / HeLa cells
[0033] (1) Screening of ShKu70 / HeLa cells
[0034] The Ku70 ShRNA plasmid was transferred into HeLa cells by lipofection method. The Ku70ShRNA plasmid was purchased from Jikai Company, and the plasmid map (GV248 plasmid) is as follows: figure 2 As indicated, the coding sequence of Ku70 ShRNA (as shown in SEQ ID No.5) was inserted into the multiple cloning site. The plasmid is transfected into cells, and ShRNA targeting Ku70mRNA can be expressed, thereby inhibiting the expression of Ku70 and reducing the level of Ku70 protein in cells.
[0035] After 24 hours of transfection, 1 μg / ml of puromycin was added to the culture medium to select HeLa cells that integrated the transfected plasmid DNA in the genome. After one month of screening, ShKu70 / HeLa cells stably inhibiting the expression of endogenous Ku70 were obtained by limiting dilution method and monoclonal s...
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