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缩短的微卫星d(CA)21序列下调基质金属蛋白酶9基因的启动子活性。

Shortened microsatellite d(CA)21 sequence down-regulates promoter activity of matrix metalloproteinase 9 gene.

作者信息

Shimajiri S, Arima N, Tanimoto A, Murata Y, Hamada T, Wang K Y, Sasaguri Y

机构信息

Department of Pathology and Cell Biology, School of Medicine, University of Occupational and Environmental of Health, Kitakyushu, Japan.

出版信息

FEBS Lett. 1999 Jul 16;455(1-2):70-4. doi: 10.1016/s0014-5793(99)00863-7.

Abstract

One characteristic elements in the promoter of the matrix metalloproteinase 9 (MMP-9) gene is the d(CA) repeat. To investigate whether this element regulates the transcription of the MMP-9 gene and its enzymatic activities, we sequenced the promoter region isolated from esophageal carcinoma cell lines. TE9 cells with low MMP-9 enzymatic activity had the number of d(CA) repeats shortened from 21 to 14 or 18. TE8, TE10 and TE11 cells with high MMP-9 activities had 21 or 23 d(CA) repeats. Luciferase assays using MMP-9 promoter containing 18, 14 or 0 d(CA) repeats showed transcriptional activities which were 50, 50 or 5%, respectively, of the level achieved with promoter containing 21 d(CA) repeats. Sequence analysis of the promoter of 223 Japanese subjects revealed that most had two alleles with 20, 21 or 22 d(CA) repeats, whereas six had one or two alleles with 14, 18 or 19 d(CA) repeats. We postulate that length alteration of the d(CA) repeat causes phenotypic differences among carcinoma cells and that microsatellite instability may contribute to the polymorphism of d(CA) repeat length.

摘要

基质金属蛋白酶9(MMP-9)基因启动子中的一个特征性元件是d(CA)重复序列。为了研究该元件是否调控MMP-9基因的转录及其酶活性,我们对从食管癌细胞系中分离出的启动子区域进行了测序。MMP-9酶活性低的TE9细胞中,d(CA)重复序列的数量从21个缩短至14个或18个。MMP-9活性高的TE8、TE10和TE11细胞有21个或23个d(CA)重复序列。使用含有18个、14个或0个d(CA)重复序列的MMP-9启动子进行荧光素酶检测,结果显示其转录活性分别为含有21个d(CA)重复序列启动子的50%、50%或5%。对223名日本受试者的启动子进行序列分析发现,大多数人有两个分别含有20个、21个或22个d(CA)重复序列的等位基因,而有6人有一个或两个分别含有14个、18个或19个d(CA)重复序列的等位基因。我们推测,d(CA)重复序列长度的改变导致癌细胞之间出现表型差异,并且微卫星不稳定性可能导致d(CA)重复序列长度的多态性。

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