CpG methylation attenuates Sp1 and Sp3 binding to the human extracellular superoxide dismutase promoter and regulates its cell-specific expression.
CpG methylation attenuates Sp1 and Sp3 binding to the human extracellular superoxide dismutase promoter and regulates its cell-specific expression.
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DOI：
10.1016/j.freeradbiomed.2010.01.007
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发表时间：
2010-04-01
影响因子：
7.4
通讯作者：
Folz, Rodney J.
中科院分区：
文献类型：
--
作者：
Zelko, Igor N.;Mueller, Michael R.;Folz, Rodney J.
关键词：
Extracellular superoxide dismutase (EC-SOD) plays an important role in maintaining normal redox homeostasis in the lung. It is expressed at very high levels in pulmonary fibroblasts, alveolar type II epithelial cells and smooth muscle cells. The molecular mechanism(s) governing this cell-specific expression of EC-SOD are mostly unknown. In our previous studies we showed that EC-SOD cell specific expression was not attributed to differential transcriptional regulation, suggesting that other, possibly epigenetic, mechanisms are involved in regulation of its expression. In this paper, we found high levels of promoter methylation in A549 cells and correspondingly low levels of methylation in MRC5 cells. Inhibition of DNA methyltransferase activity by 5-azacytidine in A549 cells reactivated EC-SOD transcription (2.75±0.16 fold, p<0.001) demonstrating the importance of methylation in repression of EC-SOD expression. Furthermore, methylation of cytosines in the promoter markedly decreased Sp1/Sp3 driven promoter activity to 30.09±2.85% (p<0.001) compare to unmethylated promoter. This attenuation of transcription in the promoter-reporter construct was, at least in part, attributed to the binding of methyl-binding protein MeCP2 in the insect cells. However, no binding of MeCP2 or MBD2 proteins to EC-SOD promoter was detected in mammalian cells in vivo. We also found marked differences in the chromatin organization of the EC-SOD promoter between these two cell lines, further supporting the important role epigenetic modifications play in the regulation of EC-SOD expression.
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影响因子：
3.8
作者：
Rabbani, ZN;Anscher, MS;Folz, RJ;Archer, E;Huang, H;Chen, LG;Golson, ML;Samulski, TS;Dewhirst, MW;Vujaskovic, Z
通讯作者：
Vujaskovic, Z
DOI：
10.1152/ajplung.00058.2001
发表时间：
2002-04-01
影响因子：
4.9
作者：
Bowler, RP;Nicks, M;Crapo, JD
通讯作者：
Crapo, JD
影响因子：
8.7
作者：
Luoma, JS;Strålin, P;Ylä-Herttuala, S
通讯作者：
Ylä-Herttuala, S
影响因子：
--
作者：
Lee, LTO;Tan-Un, KC;Chow, BKC
通讯作者：
Chow, BKC
DOI：
10.1165/ajrcmb.16.2.9032123
发表时间：
1997-02-01
影响因子：
6.4
作者：
Su, WY;Folz, R;Chang, LY
通讯作者：
Chang, LY