Human source chromosome targeting vector of human beta-globin gene cluster and application therefor
A technology of targeting vectors and globin, which is used in gene therapy, introduction of foreign genetic material using vectors, blood diseases, etc. It can solve the problems of low expression level, unstable gene integration, random integration sites of viral vectors, etc., to avoid immunity. The effect of responding, avoiding safety problems
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Embodiment 1
[0044] Example 1. Construction and Identification of Human Chromosomal Targeting Vector of Human β-globin Gene Cluster
[0045] The homology analysis and chromosome location of the two homology arms TGLS1 and TGLS2 in the human chromosome BAC targeting vector BACMS are carried out. The chromosome location map is as follows: figure 2 As shown (A in the figure indicates that it is located at 21p11, and B indicates that it is located at 7q36.2), indicating that they are not only highly homologous to the human melanoma antigen gene (B melanomaantigen, BAGE) on the short arm of the D and G chromosomes, but also related to human The Homo sapiens myeloid / lymphoid or mixed-lineage leukemia 3 (MLL3) gene at 7q36.2 at the end of the long arm of chromosome 7 is highly homologous, and the sequences of TGLS1 and TGLS2 are the last inclusion of the MLL3 gene The homology of the gene is 97%. Therefore, it is believed that using this vector to construct a new human chromosome-targeting vecto...
Embodiment 2
[0059] Embodiment 2, the acquisition of monoclonal cell line and the structural analysis of genomic DNA thereof
[0060] 1. Obtaining monoclonal cell lines
[0061] The human-derived chromosomal BAC targeting vector (BACMS / BGGC) constructed in Example 1 containing the complete β-globin gene cluster was transfected into K562 cells by the liposome method (or the BACMS / BGGC was treated with the restriction enzyme SgrAI K562 cells were electroporated after linearization). In order to prevent the possible loss of positive cell clones under the simultaneous action of two screening drugs, G418 (purchased from Sigma) and GCV (purchased from Sigma), a step-by-step screening method was adopted. After screening with 400 μg / mL G418 for 6 weeks, 12 monoclonal cell lines resistant to G418 were obtained, the genomes were extracted and each cell line was frozen; at the same time, 10 μg / mL GCV was used for negative selection of 12 cell lines. As a result, two cell lines were obtained, named ...
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