Regulation of TIMP gene expression in cell culture and during mouse embryogenesis.

A M Flenniken, C E Campbell, B R Williams
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Abstract

We have identified elements in the 5' region of the murine tissue inhibitor of metalloproteinase (TIMP) gene which control the response to serum, phorbol esters and transforming growth factor beta (TGF-beta) in cell culture. These elements lie between -858 and -601 relative to the translation initiation start site in the gene and are distinct from those that control expression in response to virus induction. The temporal and spatial expression of the TIMP gene was also analysed during mouse embryogenesis using in situ hybridization. A transgenic mouse line was constructed which expressed a TIMP/lac Z fusion gene. Using in situ beta-galactosidase assays we were able to compare the expression of the transgene with the endogenous gene. Thus we concluded that most of the sequences controlling in vivo expression of TIMP were present in the transgene and could be localised to the 5' region of the gene.

细胞培养和小鼠胚胎发生过程中TIMP基因表达的调控。
我们已经在小鼠组织金属蛋白酶抑制剂(TIMP)基因的5'区发现了一些元件,这些元件控制着细胞培养中对血清、酚酯和转化生长因子β (tgf - β)的反应。这些元件位于相对于基因翻译起始位点的-858和-601之间,与那些控制病毒诱导表达的元件不同。利用原位杂交技术分析了TIMP基因在小鼠胚胎发生过程中的时空表达。构建了表达TIMP/lac Z融合基因的转基因小鼠系。利用原位β -半乳糖苷酶测定,我们能够比较转基因与内源基因的表达。因此,我们得出结论,大部分控制TIMP在体内表达的序列都存在于转基因中,并且可以定位在基因的5'区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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