Volume 39, Issue 2 pp. 122-129
Technology Report
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Coat color-tagged green mouse with EGFP expressed from the RNA polymerase II promoter

Yi-Chun Hsiao

Yi-Chun Hsiao

Faculty of Life Sciences and Institute of Genetics, National Yang-Ming University, Taipei, Taiwan

Level Biotechnology Inc., Taipei, Taiwan

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Hsiao-Hui Chang

Hsiao-Hui Chang

Level Biotechnology Inc., Taipei, Taiwan

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Ching-Yen Tsai

Ching-Yen Tsai

Faculty of Life Sciences and Institute of Genetics, National Yang-Ming University, Taipei, Taiwan

Level Biotechnology Inc., Taipei, Taiwan

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Yiin-Jeng Jong

Yiin-Jeng Jong

Faculty of Life Sciences and Institute of Genetics, National Yang-Ming University, Taipei, Taiwan

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Long-Shyan Horng

Long-Shyan Horng

Faculty of Life Sciences and Institute of Genetics, National Yang-Ming University, Taipei, Taiwan

Level Biotechnology Inc., Taipei, Taiwan

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Shu-Fen Lin

Shu-Fen Lin

Faculty of Life Sciences and Institute of Genetics, National Yang-Ming University, Taipei, Taiwan

Level Biotechnology Inc., Taipei, Taiwan

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Ting-Fen Tsai

Corresponding Author

Ting-Fen Tsai

Faculty of Life Sciences and Institute of Genetics, National Yang-Ming University, Taipei, Taiwan

Department of Medical Research and Education, Veterans General Hospital-Taipei, Taiwan

Division of Molecular and Genomic Medicine, National Health Research Institute, Taipei, Taiwan

Faculty of Life Sciences & Institute of Genetics, National Yang-Ming University, No. 155, Sec. 2, Lih-Nong St., Taipei 112, TaiwanSearch for more papers by this author
First published: 25 May 2004
Citations: 24

Abstract

Laborious molecular genotyping and variegated gene expression are two widely encountered issues for transgenic mouse studies. To facilitate genotyping in the FVB/N albino background and to reduce variegated expression, we successfully generated double-tagged transgenic mice for direct visual genotyping with the coat color phenotype derived from tyrosinase cDNA driven by the tyrosinase promoter and with simultaneous high enhanced green fluorescent protein (EGFP) expression driven by the promoter of RNA polymerase II large subunit gene. Incorporation of insulator into a transgene construct achieved high efficiency of transgene expression in more than 90% of the founders. EGFP was detected as early as the one-cell fertilized egg and lasted for the whole embryo development, as well as in all of the adult tissues examined. The coat color-tagged green mice offer opportunities in applications such as tissue transplantation, lineage tracing, chimera biology, RNA interference, and other transgenic studies. genesis 39:122–129, 2004. © 2004 Wiley-Liss, Inc.

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