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

被引:167
作者
Shimajiri, S
Arima, N
Tanimoto, A
Murata, Y
Hamada, T
Wang, KY
Sasaguri, Y
机构
[1] Univ Occupat & Environm Hlth, Sch Med, Dept Pathol & Cell Biol, Yahatanishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[2] Kyurin Corp, Kyurin Omtest Lab Dept, Yahatanishi Ku, Kitakyushu, Fukuoka 8060046, Japan
关键词
microsatellite; d(CA) repeat; matrix metalloproteinase 9; gene transcription; esophageal cancer;
D O I
10.1016/S0014-5793(99)00863-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
One characteristic elements in re 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, (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:70 / 74
页数:5
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