Method for specificity overexpression of miRNA of slow virus mediated mammal cells
A mammalian and lentiviral technology, applied in the direction of retroRNA viruses, botanical equipment and methods, biochemical equipment and methods, etc., can solve the problem of inability to achieve specific expression of miRNAmiRNA
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specific Embodiment approach 1
[0011] Specific Embodiment 1: In this embodiment, a method of lentivirus-mediated mammalian cell-specific overexpression of miRNA is as follows: using the shRNA lentivirus expression system, the miRNA mature sequence is used as the upstream sense sequence, and the downstream and miRNA The antisense (antisense) sequence complementary to the mature sequence is mutated according to the rules of T to C and A to G, and the mutated RNA secondary neck loop structure is cloned into the shRNA lentiviral vector, and then the virus is packaged to establish a stable mutation The cell line of the RNA secondary neck loop structure; wherein 2-6 mutation sites are selected from the 2-8 bases starting from the 5' end of the antisense sequence for mutation.
[0012] Beneficial effects of this embodiment: This embodiment constructs a lentivirus-mediated method for specifically overexpressing miRNA in mammalian cells. Compared with chemical methods, it can not only overexpress a single specific mi...
specific Embodiment approach 2
[0013] Embodiment 2: The difference between this embodiment and Embodiment 1 is that the mutated sequence needs to be predicted by software for predicting the RNA secondary neck loop structure, so as to ensure that the RNA secondary neck loop structure is not destroyed. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0014] Embodiment 3: This embodiment differs from Embodiment 1 or Embodiment 2 in that: the software for predicting the RNA secondary neck loop structure is DNAMAN, RNAStructure or RNA draw. Others are the same as in the first or second embodiment.
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