[Construction of expression vector of hTERT/hIL-18 fusion gene in eukaryotic cells and its function].
Xiangmin Tong, Jie Jin, Hangping Yao, Wenbin Qian, Hai-tao Qian
Abstract
Xiangmin Tong, Jie Jin, Hangping Yao, Wenbin Qian, Hai-tao Qian
Abstract
OBJECTIVE: To construct expression vector of hTERT-hIL-18 fusion gene in eukaryotic cells and to study its biological function. METHODS: hIL-18 gene was amplified by RT-PCR, then T-A cloned and inserted into PCDNA3.1(+)/hTERT vector. The sequence of fusion gene was examined by enzyme incision and DNA sequencing. The vector with fusion gene was transformed into 3T3 cells by the method of lipofecting, and proved by Western blot. The secretion gamma-interferon was measured with ELISA and cell apoptosis was detected with flow cytometry. RESULT: Expression vector PCDNA3.1(+) of hTERT/hIL-18 fusion gene was constructed successfully. The correct sequence was proved by enzyme incision and sequencing and there was a correct open reading frame. Fusion protein of hTERT/hIL-18 was effectively expressed in eukaryotic cells and was proved by Western blot and immunofluorescence stain. The fusion protein stimulated KG-1 cells to secrete gamma-interferon and had anti-apoptosis effect. CONCLUSION: Fusion protein hTERT-hIL-18 is highly effectively expressed in eukaryotic cells and is biologically active.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
OBJECTIVE: To construct expression vector of hTERT-hIL-18 fusion gene in eukaryotic cells and to study its biological function. METHODS: hIL-18 gene was amplified by RT-PCR, then T-A cloned and inserted into PCDNA3.1(+)/hTERT vector. The sequence of fusion gene was examined by enzyme incision and DNA sequencing. The vector with fusion gene was transformed into 3T3 cells by the method of lipofecting, and proved by Western blot. The secretion gamma-interferon was measured with ELISA and cell apoptosis was detected with flow cytometry. RESULT: Expression vector PCDNA3.1(+) of hTERT/hIL-18 fusion gene was constructed successfully. The correct sequence was proved by enzyme incision and sequencing and there was a correct open reading frame. Fusion protein of hTERT/hIL-18 was effectively expressed in eukaryotic cells and was proved by Western blot and immunofluorescence stain. The fusion protein stimulated KG-1 cells to secrete gamma-interferon and had anti-apoptosis effect. CONCLUSION: Fusion protein hTERT-hIL-18 is highly effectively expressed in eukaryotic cells and is biologically active.
Key concepts: Molecular biology, Telomerase reverse transcriptase, Fusion gene, Fusion protein, Biology, Western blot, Gene, Expression vector