Viral Hepatitis
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jan 15, 2003; 9(1): 112-116
Published online Jan 15, 2003. doi: 10.3748/wjg.v9.i1.112
Expression of hepatitis B virus X protein in transgenic mice
Jun Xiong, Yu-Cheng Yao, Xiao-Yuan Zi, Jian-Xiu Li, Xin-Min Wang, Xu-Ting Ye, Shu-Min Zhao, Yong-Bi Yan, Hong-Yu Yu, Yi-Ping Hu
Jun Xiong, Yu-Cheng Yao, Xiao-Yuan Zi, Jian-Xiu Li, Xin-Min Wang, Xu-Ting Ye, Shu-Min Zhao, Yong-Bi Yan, Yi-Ping Hu, Department of Cell Biology, Second Military Medical University, Shanghai 200433, China
Hong-Yu Yu, Department of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China
Author contributions: All authors contributed equally to the work.
Supported by Projects of the Science Development Foundation of Shanghai (No.994919033) and Tackling Key Problems in Science and Technology from the State Science and Technology Ministry (No.TJ99-LA01)
Correspondence to: Yi-Ping Hu, Department of Cell Biology, Department of Basic Medicine, Second Military Medical University, Shanghai 200433, China. yphu@smmu.edu.cn
Telephone: +86-21-25070291 Fax: +86-21-25070291
Received: January 14, 2002
Revised: June 23, 2002
Accepted: July 26, 2002
Published online: January 15, 2003
Abstract

AIM: To establish a mice model harboring hepatitis B virus x gene (adr subtype) for studying the function of hepatitis B virus X protein, a transactivator of viral and cellular promoter/enhancer elements.

METHODS: Expression vector pcDNA3-HBx, containing CMV promoter and hepatitis B virus x gene open reading fragment, was constructed by recombination DNA technique. Hela cells were cultured in DMEM and transfected with pcDNA3-HBx or control pcDNA3 plasmids using FuGENE6 Transfection Reagent. Expression of pcDNA3-HBx vectors in the transfected Hela cells was confirmed by Western blotting. After restriction endonuclease digestion, the coding elements were microinjected into male pronuclei of mice zygotes. The pups were evaluated by multiplex polymerase chain reaction (PCR) at genomic DNA level. The x gene transgenic mice founders were confirmed at protein level by Western blotting, immunohistochemistry and immunogold transmission electron microscopy.

RESULTS: Expression vector pcDNA3-HBx was constructed by recombination DNA technique and identified right by restriction endonuclease digestion and DNA direct sequencing. With Western blotting, hepatitis X protein was detected in Hela cells transfected with pcDNA3-HBx plasmids, suggesting pcDNA3-HBx plasmids could express in eukaryotic cells. Following microinjection of coding sequence of pcDNA3-HBx, the embryos were transferred to oviducts of psedopregnant females. Four pups were born and survived. Two of them were verified to have the HBx gene integrated in their genomic DNA by multiplex PCR assay, and named C57-TgN (HBx)S MMU1 and C57-TgN (HB x) SMMU3 respectively. They expressed 17KD X protein in liver tissue by Western blotting assay. With the immunohistochemistry, X protein was detected mainly in hepatocytes cytoplasm of transgenic mice, which was furthermore confirmed by immunogold transmission electon microscopy.

CONCLUSION: We have constructed the expression vector pcDNA3-HBx that can be used to study the function of HBx gene in eukaryotic cells in vitro. We also established HBx gene (adr subtype) transgenic mice named C57-TgN (HBx) SMMU harboring HBx gene in their genome and express X protein in hepatocytes, Which might be a valuable animal system for studying the roles of HBx gene in hepatitis B virus life cycle and development of hepatocellular carcinoma in vivo.

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