首页> 外文期刊>Nucleic acids research >Thionein gene expression in Cd++-variants of the CHO cell: correlation of thionein synthesis rates with translatable mRNA levels during induction, deinduction, and superinduction
【24h】

Thionein gene expression in Cd++-variants of the CHO cell: correlation of thionein synthesis rates with translatable mRNA levels during induction, deinduction, and superinduction

机译:硫蛋白基因在CHO细胞Cd ++变体中的表达:硫蛋白合成速率与诱导,还原和超诱导过程中可翻译mRNA水平的相关性

获取原文
           

摘要

The relationship of thionein synthesis rates to translatable cytoplasmic thionein mRNA levels was investigated for the first time in a cultured cell system. Thionein synthesis was induced in Cdr, a cadmium-resistant variant of CHO, by exposure to 2 μM CdCl2. Following a short (1.5 hr) lag, thionein synthesis increases to a rate that is at least 30 times the uninduced rate 7–8 hr after addition of Cd++. This increase is blocked by the coincident addition of actinomycin D. Cytoplasmic thionein mRNA levels, measured by translation in a modified wheat germ system, increase rapidly following induction to values approximately 25 times uninduced levels within 6–8 hr. The increases in thionein mRNA precede proportionate increases in thionein synthesis by 0.5–1.0 hr. Continued exposure to Cd++ results in a decreased thionein synthesis rate after 8 hr. By 30 hr, the rate is one-half that seen 6–8 hr after induction. Removal of Cd++ after 8 hr results in a rapid decrease in thionein synthesis (t1/2 - 4 hr). Both decreases are inhibited by the addition of actinomycin. In all instances--induction, deinduction, and actinoraycin-mediated “super-induction”--translatable thionein mRNA levels and thionein synthesis rates increase, decrease, or are maintained coordinately. The results suggest that thionein synthesis in Cdr is controlled primarily by the level of translatable cytoplasmic thionein mRNA.
机译:在培养的细胞系统中,首次研究了硫蛋白合成速率与可翻译胞质硫蛋白mRNA水平的关系。通过暴露于2μMCdCl 2 ,在Cd r (一种对镉具有抗性的CHO中)诱导硫蛋白合成。在短暂的(1.5小时)滞后之后,添加Cd ++ 后7–8小时,硫蛋白的合成速率增加到未诱导速率的至少30倍。通过同时添加放线菌素D可以阻止这种增加。通过修饰的小麦胚芽系统中的翻译测量,胞质硫蛋白mRNA水平在诱导后6-8小时内迅速增加至未诱导水平的25倍。硫蛋白mRNA的增加先于硫蛋白合成按比例增加0.5-1.0小时。持续暴露于Cd ++ 会导致8小时后硫蛋白合成速率降低。到30小时,该频率是诱导后6-8小时的一半。 8小时后去除Cd ++ 导致硫蛋白合成迅速降低(t 1/2 -4小时)。放线菌素的添加均抑制了两种减少。在所有情况下,诱导,去诱导和放线菌素介导的“超诱导”,可翻译的硫蛋白mRNA水平和硫蛋白合成速率均会提高,降低或保持协调。结果表明,Cd r 中硫蛋白的合成主要受可翻译胞质硫蛋白mRNA水平的控制。

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