Viral Hepatitis
Copyright ©2005 Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. May 21, 2005; 11(19): 2885-2891
Published online May 21, 2005. doi: 10.3748/wjg.v11.i19.2885
Generation of the regulatory protein rtTA transgenic mice
Kang Xu, Xin-Yan Deng, Ying Yue, Zhong-Min Guo, Bing Huang, Xun Hong, Dong Xiao, Xi-Gu Chen
Kang Xu, Xin-Yan Deng, Ying Yue, Zhong-Min Guo, Bing Huang, Xun Hong, Dong Xiao, Xi-Gu Chen, Center of Experimental Animals, Sun Yat-Sen (Zhongshan) University, Guangzhou 510080, Guangdong Province, China
Kang Xu, The First Affiliated Hospital of Sun Yat-Sen University, Sun Yat-Sen (Zhongshan) University, Guangzhou 510080, Guangdong Province, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 30271177 and No. 39870676; Guangdong Province Natural Science Foundation of China, No. 021903; Postdoctoral Fellowship Foundation of China
Correspondence to: Professor Xi-Gu Chen, Center of Experimental Animals, Sun Yat-Sen (Zhongshan) University, No. 74, Zhongshan Road 2, Guangzhou 510080, Guangdong Province, China. xiguchen@163.com
Telephone: +86-20-8733-1393 Fax: +86-20-8733-1230
Received: February 2, 2004
Revised: February 3, 2004
Accepted: April 5, 2004
Published online: May 21, 2005
Abstract

AIM: To translate Tet-on system into a conditional mouse model, in which hepatitis B or C virus (HBV or HCV) gene could be spatiotemporally expressed to overcome “immune tolerance” formed during the embryonic development and “immune escape” against hepatitis virus antigen(s), an effector mouse, carrying the reverse tetracycline-responsive transcriptional activator (rtTA) gene under the tight control of liver-specific human apoE promoter, is required to be generated.

METHODS: To address this end, rtTA fragment amplified by PCR was effectively inserted into the vector of pLiv.7 containing apoE promoter to create the rtTA expressing vector, i.e., pApoE-rtTA. ApoE-rtTA transgenic fragment (-6.9 kb) released from pApoE-rtTA was transferred into mice by pronucleus injection, followed by obtaining one transgene (+) founder animal from microinjection through PCR and Southern blot analysis.

RESULTS: rtTA transgene which could be transmitted to subsequent generation (F1) derived from founder was expressed in a liver-specific fashion.

CONCLUSION: Taken together, these findings demonstrate that rtTA transgenic mice, in which rtTA expression is appropriately targeted to the murine liver, are successfully produced, which lays a solid foundation to ‘off-on-off’ regulate expression of target gene (s) (e.g., HBV and/or HCV) in transgenic mice mediated by Tet-on system.

Keywords: Hepatitis virus; Tet-on system; Transgenic mice; Liver-specific human apoE promoter