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©2006 Baishideng Publishing Group Co.
World J Gastroenterol. Dec 14, 2006; 12(46): 7488-7496
Published online Dec 14, 2006. doi: 10.3748/wjg.v12.i46.7488
Published online Dec 14, 2006. doi: 10.3748/wjg.v12.i46.7488
Figure 1 Construction of APOBEC3G and its N-terminal and C-terminal cytosine deaminase domain expression plasmids.
Full-length APOBEC3G sequence was cloned into EcoRI/HindIII restriction sites of the CMV-driven expression vector fused with a hemagglutinin fusion epitope tag at its N- terminal end (pXF3H) to construct APOBEC3G expression plasmid (pA3G). pA3G was digested with EcoRI/BamHIand BamHI/HindIII, these fragments were inserted into pXF3H to construct the N-terminal and C-terminal cytosine deaminase domain expression plasmids (pXFNA3G and pXFCA3G), respectively. pA3G was digested with EcoRI/BglII, and used for the construction of the N-terminal region of APOBEC3G which did not contain any cytosine deaminase domain plasmid (pXFEA3G). pCMV: CMV promoter; CD1: N-terminal cytosine deaminase domain; CD2: C-terminal cytosine deaminase domain.
- Citation: Lei YC, Tian YJ, Ding HH, Wang BJ, Yang Y, Hao YH, Zhao XP, Lu MJ, Gong FL, Yang DL. N-terminal and C-terminal cytosine deaminase domain of APOBEC3G inhibit hepatitis B virus replication. World J Gastroenterol 2006; 12(46): 7488-7496
- URL: https://www.wjgnet.com/1007-9327/full/v12/i46/7488.htm
- DOI: https://dx.doi.org/10.3748/wjg.v12.i46.7488