This work was supported by the grants from the National High Technology Research and Development Program of China (“863" Programme) (No. 2002AA216031) and the National Basic Research Program of China (973 Program) (No. 2006CB504300).
Recently,the interactions between hepatitis C virus (HCV) genes and the host cell factors were the focus of this field. Cell factors in the different biochemical pathway were approved to be interfered when HCV infection. To make sure which HCV gene(s) was the major factor during the interaction process,ten eukaryotic expression plasmids containing different functional genes of HCV: Core,E1,E2,p7,NS2,NS3,NS4A,NS4B,NS5A and NS5B were transfected into the CHO-K1 cells respectively. Then ten stable cell lines expressing different HCV functional proteins were constructed under the selective pressure of G418. DNA and mRNA of the HCV genes were both detected by PCR and RT-PCR respectively in the corresponding stable cell lines,freezation and anabiosis would not lose the HCV genes. Besides,the E1,E2 and NS5B proteins were detected by Western-blot which demonstrated that the HCV genes have formed stable expression in the host cells. The activity of UDP-glucose ceramide glucosyltransferase (UGCG) in the stable cell lines increased in different degree by TLC assay. For example,the activity of UGCG in CHO-K1-E2 and CHO-K1-p7 was doubled according to the control cells,and in CHO-K1-NS2 and CHO-K1-NS5A was about 1.6 times compared with the control cells. The establishment of the stable cell lines containing different single HCV gene will provide foundation for investigating the interactions between the virus and the host factors,and for the filtration of antiviral medicine.
郭佳,鄢然,徐国东,郑从义. 丙型肝炎病毒功能基因在CHO细胞中的表达研究[J]. Chinese Journal of Biotechnology, 2007, 23(6):
Copy® 2024 All Rights Reserved