Viral Hepatitis
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 15, 2003; 9(3): 513-515
Published online Mar 15, 2003. doi: 10.3748/wjg.v9.i3.513
Expression of RNase H of human hepatitis B virus polymerase in Escherichia coli
Hong Cheng, Hui-Zhong Zhang, Wan-An Shen, Yan-Fang Liu, Fu-Cheng Ma
Hong Cheng, Yan-Fang Liu, Fu-Cheng Ma, Department of Pathology, Xijing Hospital, Fourth Military Medical University, Xi’an 710033, Shaanxi Province, China
Hui-Zhong Zhang, Wan-An Shen, Orthopedics Oncology Institute of Chinese PLA, Fourth Military Medical University, Tangdu Hospital, Xi’an 710038, Shaanxi Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Hong Cheng, Department of Pathology, Xijing Hospital, Fourth Military Medical University, Xi’an 710033, Shaanxi Province, China. nelson@fmmu.edu.cn
Telephone: +86-29-3375497
Received: October 17, 2002
Revised: November 8, 2002
Accepted: November 16, 2002
Published online: March 15, 2003
Abstract

AIM: To amplify HBV-RNase H gene fragment and expression of RNase H for further use in the studies of HBV associated liver diseases.

METHODS: The encoding gene of HBV-RNase H was separately amplified for the first half and second half (H1 and H2) by PCR from full length HBV gene and cloned into pT7Blue-T vector. Clones were first screened by digestion with Xba I and Hind III enzyme for the correct size, and analyzed further by DNA sequencing. The RNase H1 and H2 fragments isolated from XbaI and Hind III digestion products of pT7 Blue-RNase H plasmid were ligated to the GSTag expressing vectors separately, and expressed in E.coli BL21. The expressed proteins were checked by PAGE gel and Western blot.

RESULTS: Both H1 and H2 nucleotide seqences consisting of known genes and proteins, in correct size, were further confirmed by Western blot to be the GST and RNase H1 or H2 fusion proteins.

CONCLUSION: The successful cloning and expression of HBV-RNase H will contribute to further research and application in HBV-associated diseases.

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