首页> 外文OA文献 >Thionein gene expression in Cd++-variants of the CHO cell: correlation of thionein synthesis rates with translatable mRNA levels during induction, deinduction, and superinduction.
【2h】

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。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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 microM 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 a 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 increase 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 (t 1/2 approximately 4 hr). Both decreases are inhibited by the addition of actinomycin. In all instances--induction, deinduction, and actinomycin-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2 microM CdCl2在CHO的抗镉变体Cdr中诱导硫蛋白合成。在短暂的(1.5小时)滞后后,硫氰酸合成速度增加到至少是添加Cd ++后7-8小时未诱导速率的30倍。通过同时添加放线菌素D来阻止这种增加。通过修饰的小麦胚芽系统中的翻译测量,胞质硫蛋白mRNA水平在诱导后迅速增加,在6-​​8小时内达到未诱导水平的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,诱导率是诱导后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约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,Cdr中的硫蛋白合成主要受可翻译的胞质硫蛋白mRNA水平控制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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