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  4. 應用條件化基因剔除及轉基因策略探討小鼠C型血小板生長因子(PDGF-C)生理作用之分子調控機制(1/3)
 
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應用條件化基因剔除及轉基因策略探討小鼠C型血小板生長因子(PDGF-C)生理作用之分子調控機制(1/3)

Date Issued
2003
Date
2003
Author(s)
鄭登貴
DOI
912313B002384
URI
http://ntur.lib.ntu.edu.tw//handle/246246/16456
Abstract
Several inducible gene expression systems have been developed in vitro in recent years to overcome limitations with traditional transgenic mice. One of these, the tetracycline-regulated system, has been used successfully in vivo. The expression of the targeted protein are controlled by a promoter containing seven DNA operator sequences from the Escherichia coli transposon 10 ( Tn10). To control the expression of PDGF-C in transgenic (Tg) mice, we used a tetracycline-controlled transactivator (tTA or rtTA) and a tTA/rtTA-dependent promoter linked to a PDGF-C gene. Doxycycline (Dox)-sensitive co-regulation of two transcriptionally coupled transgenes will be investigated in the mouse. For this, we generated four independent mouse line clone carrying coding regions for mouse PDGF-C gene and green fluorescent protein (GFP) in a bicistronic, bidirectional module under the control of the Tet-responsive promoter and/or 4311 regulatory regions of trophoblast- specific promoter. It is anticipated that the rtTA andor tTA-sensitive bi-directional expression module is well suited to express genes of interest in a regulated manner and that GFP can be used to track transcriptional activity of the module in the living mouse.
Subjects
PDGF-C
Tetracycline-regulated system
green fluorescent protein
transgenic mice
Publisher
臺北市:國立臺灣大學動物科學技術學系暨研究所
Type
report
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