Construction and identification of a expression vector driven by human telomerase reverse transcriptase gene promotor
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Abstract
Objective: To construc and identify the expression vector which contains a luciferase gene driven by human telomerase reverse transcriptase(hTERT) gene promotor.Methods: The fragment of hTERT promoter about 1 100 bp was acquired by nested PCR amplification,the correct sequence was inserted into the luciferase gene expression vector.In order to get a lot of containing hTERT promoter luciferase recombinant,the construction of pGL3-hTERTp recombinant was transformed into JM190 bacteria.Restriction endonuclease and PCR were used to identify the recombinant and sequencing.Results: After identifying which used restriction endonuclease and PCR method,we successfully constructed the recombinant of hTERT promoter luciferase gene expression vector.Conclusions: A novel recombinant luciferase gene expression vector driven by hTERT promoter is made successfully,and the newly constructed recombinant is useful for study the molecular mechanism that As2O3 inhibits the expression of telomerase of HL-60 cells.
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