...
首页> 外文期刊>Journal of health science. >Characterization of Gene Expression Profiles of Metallothionein-Null Cadmium-Resistant Cells
【24h】

Characterization of Gene Expression Profiles of Metallothionein-Null Cadmium-Resistant Cells

机译:耐金属硫蛋白的抗镉细胞基因表达谱的表征

获取原文
获取原文并翻译 | 示例

摘要

To understand metallothionein (MT)-independent mechanisms for cadmium (Cd) resistance in mammalian cells, we previously established MT-null Cd-resistant cells from embryonic fibroblast cells of MT-I and -II knockout mice. The Cd resistance of these cells was conferred primarily by a marked reduction of Cd accumulation. To identify genes responsible for Cd resistance as well as Cd transport, we carried out several DNA microarray analyses using cDNAs obtained from two clones of Cd-resistant cells and parental cells. A competitive hybridization of Cy3-and Cy5-probed cDNAs on a DNA chip was carried out with dye-swapping. After a careful examination of the reproducibility and reliability of the data obtained using five different chips, it was found that the expression of 78 genes was enhanced and that of 48 genes was reduced in Cd-resistant cells compared with those in parental cells. These genes include those involved in signal transduction, ubiquitin pathway, and cell-to-cell interactions. Several genes for transporters including solute carrier family transporters and ATP-binding cassette transporters were up- or down-regulated. The examination of mRNA levels using quantitative real-time PCR revealed that the expression of Slc39al4 encoding ZIP14, a member of the zinc transporter ZIP (ZRT-, IRT-like protein) family, was markedly down-regulated in both clones of Cd-resistant cells. Although it is not yet clear whether ZIP14 has the ability to transport Cd, these results suggest that the lowered expression of ZIP14 may be involved in Cd resistance in MT-null cells.
机译:为了了解哺乳动物细胞对镉(Cd)抗性的金属硫蛋白(MT)依赖性机制,我们先前从MT-1和-II基因敲除小鼠的胚胎成纤维细胞中建立了对MT无效的Cd抗性细胞。这些细胞对Cd的抗性主要是由于Cd积累的显着减少所致。为了鉴定负责Cd抗性和Cd转运的基因,我们使用了从两个Cd抗性细胞和亲本细胞克隆获得的cDNA进行了几种DNA微阵列分析。通过交换染料,在DNA芯片上进行了Cy3和Cy5探测的cDNA的竞争性杂交。在仔细检查了使用五种不同芯片获得的数据的可重复性和可靠性之后,发现与亲代细胞相比,Cd耐药细胞中78个基因的表达增强,而48个基因的表达减少。这些基因包括那些涉及信号转导,泛素途径和细胞间相互作用的基因。转运蛋白的几个基因包括溶质载体家族转运蛋白和ATP结合盒转运蛋白被上调或下调。使用定量实时PCR检测mRNA水平发现,编码锌的转运蛋白ZIP(ZRT-,IRT-like蛋白)家族成员ZIP14的Slc39al4的表达在耐Cd的两个克隆中均明显下调细胞。尽管尚不清楚ZIP14是否具有转运Cd的能力,但这些结果表明ZIP14的降低表达可能与MT空细胞的Cd抗性有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号