Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jan 15, 2004; 10(2): 264-267
Published online Jan 15, 2004. doi: 10.3748/wjg.v10.i2.264
Establishment of transgenic mice carrying gene encoding human zinc finger protein 191
Jian-Zhong Li, Xia Chen, Hua Yang, Shui-Liang Wang, Xue-Lian Gong, Hao Feng, Bao-Yu Guo, Long Yu, Zhu-Gang Wang, Ji-Liang Fu
Jian-Zhong Li, Hua Yang, Shui-Liang Wang, Ji-Liang Fu, Department of Medical Genetics, Second Military Medical University, Shanghai 200433, China
Zhu-Gang Wang, Ji-Liang Fu, Shanghai Nanfang Research Center for Biomodel Organism, Shanghai 201203, China
Long Yu, Genetics Institute, Fudan University, Shanghai 200433, China
Jian-Zhong Li, Xue-Lian Gong, Hao Feng, Bao-Yu Guo, Department of Biochemical Pharmacy, Second Military Medical University, Shanghai 200433, China
Xia Chen, Shanghai Research Center of Biotechnology, Chinese Academy of Sciences, Shanghai 200233, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No.39830360
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: June 16, 2003
Revised: July 17, 2003
Accepted: July 24, 2003
Published online: January 15, 2004
Abstract

AIM: Human zinc finger protein 191 (ZNF191) was cloned and characterized as a Krüppel-like transcription factor, which might be relevant to many diseases such as liver cancer, neuropsychiatric and cardiovascular diseases. Although progress has been made recently, the biological function of ZNF191 remains largely unidentified. The aim of this study was to establish a ZNF 191 transgenic mouse model, which would promote the functional study of ZNF191.

METHODS: Transgene fragments were microinjected into fertilized eggs of mice. The manipulated embryos were transferred into the oviducts of pseudo-pregnant female mice. The offsprings were identified by PCR and Southern blot analysis. ZNF 191 gene expression was analyzed by RT-PCR. Transgenic founder mice were used to establish transgenic mouse lineages. The first generation (F1) and the second generation (F2) mice were identified by PCR analysis. Ten-week transgenic mice were used for pathological examination.

RESULTS: Four mice were identified as carrying copies of ZNF191 gene. The results of RT-PCR showed that ZNF 191 gene was expressed in the liver, testis and brain in one of the transgenic mouse lineages. Genetic analysis of transgenic mice demonstrated that ZNF 191 gene was integrated into the chromosome at a single site and could be transmitted stably. Pathological analysis showed that the expression of ZNF 191 did not cause obvious pathological changes in multiple tissues of transgenic mice.

CONCLUSION: ZNF 191 transgenic mouse model would facilitate the investigation of biological functions of ZNF191 in vivo.

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