Heme oxygenase-1 gene enhancer manifests silencing activity in a chromatin environment prior to oxidative stress

被引:20
作者
Dohl, Y
Alam, J
Yoshizumi, M
Sun, JY
Igarashi, K
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Dept Biomed Chem, Hiroshima 724, Japan
[2] Hiroshima Univ, Grad Sch Biomed Sci, Dept Cardiovasc Physiol & Med, Hiroshima 724, Japan
[3] Louisiana State Univ, Med Ctr, Alton Ochsner Med Fdn & Ochsner Clin, Dept Mol Genet, Baton Rouge, LA 70803 USA
[4] Louisiana State Univ, Med Ctr, Dept Biochem & Mol Biol, Baton Rouge, LA 70803 USA
关键词
D O I
10.1089/ars.2006.8.60
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The expression of heme oxygenase-1 (HO-1) is regulated by El and E2 enhancers, both of which contain multiple Maf recognition elements (MAREs). In living cells, MAREs are bound by Bach1/MafK heterodimers, hence maintaining a quiescent state of the HO-1 gene (hmox-1): However, in transient transfection assays, they act as transcriptional enhancers. Therefore MAREs may manifest their function only in a chromatin environment. By using NIH3T3 cell pools stably transfected with EGFP reporter genes driven by the wild-type or mutated E2 enhancer, we demonstrate that the E2 MAREs function as transcriptional silencers depending on the binding of Bach1/MafK heterodimer in vivo only in a chromatin environment. After cadmium treatment, they switched into transcriptional enhancers. Surprisingly, single MARE site did not exhibit such fuliction. Furthermore, by using DNase I hypersensitivity assay, we demonstrate that simple chromatin condensations were not involved in the Bach1-mediated repression. We conclude that, in a chromatin environment, the E2 MAREs function as transcriptional silencers depending on binding of BachI/MafK heterodimer.
引用
收藏
页码:60 / 67
页数:8
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