2007PubMedRequires access

[Expression of HCV NS5A gene in HepG2 cell and the effect of the NS5A expression on PI3K in vitro].

Xuefang Hu, Xiao-zhao Deng, Zhenyu Diao, Yun Zhang, Zhou Zong-an, Yu Liu

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Abstract

AIM: To reveal the influence of HCV-NS5A on PI3K, we probe into the relationship between NS5A and PI3K in vitro. METHODS: Full length NS5A gene of HCV was amplified by PCR, using the plasmid containing HCV full-length open reading frame (ORF) as template, and cloned into the eukaryotic expressing plasmid pcDNA3.0(-) by DNA recombination technique. The recombinant vector was identified by digestion with restriction enzymes and polymerase chain reaction and by directly sequencing. Then both the recombinant vector pcDNA3.0(-)-NS5A and the control vector pcDNA3.0(-) were transfected HepG2 cell using Lipofectamin2000. RESULTS: Expressing NS5A was proven by RT-PCR and Western blot analysis in transfected HepG2 cell. Further more we examined the PI3K protein expressed in the HepG2 cell expressing recombinant NS5A. CONCLUSION: NS5A can activate PI3K in vitro and its signal cascade pathway.

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What this paper is about

AIM: To reveal the influence of HCV-NS5A on PI3K, we probe into the relationship between NS5A and PI3K in vitro. METHODS: Full length NS5A gene of HCV was amplified by PCR, using the plasmid containing HCV full-length open reading frame (ORF) as template, and cloned into the eukaryotic expressing plasmid pcDNA3.0(-) by DNA recombination technique. The recombinant vector was identified by digestion with restriction enzymes and polymerase chain reaction and by directly sequencing. Then both the recombinant vector pcDNA3.0(-)-NS5A and the control vector pcDNA3.0(-) were transfected HepG2 cell using Lipofectamin2000. RESULTS: Expressing NS5A was proven by RT-PCR and Western blot analysis in transfected HepG2 cell. Further more we examined the PI3K protein expressed in the HepG2 cell expressing recombinant NS5A. CONCLUSION: NS5A can activate PI3K in vitro and its signal cascade pathway.

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Available abstract

AIM: To reveal the influence of HCV-NS5A on PI3K, we probe into the relationship between NS5A and PI3K in vitro. METHODS: Full length NS5A gene of HCV was amplified by PCR, using the plasmid containing HCV full-length open reading frame (ORF) as template, and cloned into the eukaryotic expressing plasmid pcDNA3.0(-) by DNA recombination technique. The recombinant vector was identified by digestion with restriction enzymes and polymerase chain reaction and by directly sequencing. Then both the recombinant vector pcDNA3.0(-)-NS5A and the control vector pcDNA3.0(-) were transfected HepG2 cell using Lipofectamin2000. RESULTS: Expressing NS5A was proven by RT-PCR and Western blot analysis in transfected HepG2 cell. Further more we examined the PI3K protein expressed in the HepG2 cell expressing recombinant NS5A. CONCLUSION: NS5A can activate PI3K in vitro and its signal cascade pathway.

Key concepts: NS5A, Recombinant DNA, Molecular biology, Transfection, Plasmid, Biology, Restriction enzyme, Expression vector

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[Expression of HCV NS5A gene in HepG2 cell and the effect of the NS5A expression on PI3K in vitro]. — Research Paper | ScholarLens