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首页> 外文期刊>Toxicology and Applied Pharmacology >Involvement of DNA hypermethylation in down-regulation of the zinc transporter ZIP8 in cadmium-resistant metallothionein-null cells.
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Involvement of DNA hypermethylation in down-regulation of the zinc transporter ZIP8 in cadmium-resistant metallothionein-null cells.

机译:DNA高甲基化参与抗镉抗性金属硫蛋白无效细胞中锌转运蛋白ZIP8的下调。

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The Zrt/Irt-related protein 8 (ZIP8) encoded by slc39a8 is now emerging as an important zinc transporter involved in cellular cadmium incorporation. We have previously shown that mRNA and protein levels of ZIP8 were decreased in cadmium-resistant metallothionein-null (A7) cells, leading to a decrease in cadmium accumulation. However, the mechanism by which ZIP8 expression is suppressed in these cells remains to be elucidated. In the present study, we investigated the possibility that epigenetic silencing of the slc39a8 gene by DNA hypermethylation is involved in the down-regulation of ZIP8 expression. A7 cells showed a higher mRNA level of DNA methyltransferase 3b than parental cells. Hypermethylation of the CpG island of the slc39a8 gene was detected in A7 cells. Treatment of A7 cells with 5-aza-deoxycytidine, an inhibitor of DNA methyltransferase, caused demethylation of the CpG island of the slc39a8 gene and enhancement of mRNA and protein levels of ZIP8. In response to the recovery of ZIP8 expression, A7 cells treated with 5-aza-deoxycytidine showed an increase in cadmium accumulation and consequently an increase in sensitivity to cadmium. These results suggest that epigenetic silencing of the slc39a8 gene by DNA hypermethylation plays an important role in the down-regulation of ZIP8 in cadmium-resistant metallothionein-null cells.
机译:slc39a8编码的Zrt / Irt相关蛋白8(ZIP8)现在正成为参与细胞镉掺入的重要锌转运蛋白。先前我们已经显示,抗镉的金属硫蛋白-无(A7)细胞中ZIP8的mRNA和蛋白水平降低,从而导致镉积累的降低。然而,在这些细胞中抑制ZIP8表达的机制仍有待阐明。在本研究中,我们调查了通过DNA高甲基化对slc39a8基因进行表观遗传沉默可能与ZIP8表达的下调有关。 A7细胞显示出比亲代细胞更高的DNA甲基转移酶3b mRNA水平。在A7细胞中检测到slc39a8基因CpG岛的甲基化过高。用DNA甲基转移酶抑制剂5-氮杂脱氧胞苷处理A7细胞,导致slc39a8基因的CpG岛脱甲基,并提高ZIP8的mRNA和蛋白水平。响应ZIP8表达的恢复,用5-氮杂-脱氧胞苷处理的A7细胞显示出镉积累的增加,因此对镉的敏感性增加。这些结果表明,DNA高甲基化对slc39a8基因的表观遗传沉默在抗镉的金属硫蛋白无效细胞中ZIP8的下调中起重要作用。

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