Basic Research
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jun 15, 2003; 9(6): 1333-1336
Published online Jun 15, 2003. doi: 10.3748/wjg.v9.i6.1333
Establishment of transgenic mice carrying the gene of human nuclear receptor NR5A2 (hB1F)
Shui-Liang Wang, Hua Yang, You-Hua Xie, Yuan Wang, Jian-Zhong Li, Long Wang, Zhu-Gang Wang, Ji-Liang Fu
Shui-Liang Wang, Hua Yang, Jian-Zhong Li, Ji-Liang Fu, Department of Medical Genetics, Second Military Medical University, Shanghai 200433, China
You-Hua Xie, Yuan Wang, Institute of Biochemistry and Cell Biology, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China
Long Wang, Zhu-Gang Wang, Ji-Liang Fu, Shanghai Nanfang Research Center for Model Organisms, Shanghai 201203, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No.39830360, and the National 863 High Technology Research and Development Program of China, No. 2001AA221261
Correspondence to: Professor. Ji-Liang Fu, Department of Medical Genetics, Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, China. jlfu@guomai.sh.cn
Telephone: +86-21-25070027 Fax: +86-21-25070027
Received: December 5, 2002
Revised: December 24, 2002
Accepted: January 2, 2003
Published online: June 15, 2003
Abstract

AIM: Human hepatitis B virus enhancer II B1 binding factor (hB1F) was cloned and characterized as a novel member of the Ftz-F1 (NR5A) nuclear receptor subfamily. Although progresses have recently been made, its biological function remains largely unidentified. The aim of this study was to establish an hB1F transgenic mouse model to promote the functional study of hB1F.

METHODS: Transgene fragments were microinjected into fertilized eggs of mice. The manipulated embryos were transferred into the oviducts of pseudopregnant female mice. The offsprings were identified by PCR and Southern blot analysis. Transgene expression was analyzed with RT-PCR and Western blot analysis. Transgenic founder mice were used to establish transgenic mouse lineages. The F1 and F2 mice were identified by PCR analysis.

RESULTS: Seven mice were identified as carrying copies of transgene. RT-PCR and Western blotting results showed that the transgene was expressed in heart, liver, lung, kidney and stomach in one of the transgenic mouse lineages. Genetic analysis of the transgenic mice demonstrated that the transgene was integrated into the chromosome at a single site, and was transmitted stably.

CONCLUSION: In this study we established an hB1F transgenic mouse model, which will facilitate the investigation of the biological function of hB1F in vivo.

Keywords: $[Keywords]