首页> 外文期刊>The biochemical journal >Effect of inhibitors of S-adenosylmethionine decarboxylase on the contents of ornithine decarboxylase and S-adenosylmethionine decarboxylase in L1210 cells
【24h】

Effect of inhibitors of S-adenosylmethionine decarboxylase on the contents of ornithine decarboxylase and S-adenosylmethionine decarboxylase in L1210 cells

机译:S-腺苷甲硫氨酸脱羧酶抑制剂对L1210细胞鸟氨酸脱羧酶和S-腺苷甲硫氨酸脱羧酶含量的影响

获取原文
           

摘要

pTreatment of L1210 cells with either of two inhibitors of S-adenosylmethionine decarboxylase (AdoMetDC), namely 5′-deoxy-5′-[N-methyl-N-[2-(amino-oxy)ethyl])aminoadenosine or 5′-deoxy-5′-[N-methyl-N-(3-hydrazinopropyl)]aminoadenosine, produced a large increase in the amount of ornithine decarboxylase (ODC) protein. The increased enzyme content was due to a decreased rate of degradation of the protein and to an increased rate of synthesis, but there was no change in its mRNA content. The inhibitors led to a substantial decline in the amounts of intracellular spermidine and spermine, but to a big increase in the amount of putrescine. These results indicate that the content of ODC is negatively regulated by spermidine and spermine at the levels of protein translation and turnover, but that putrescine is much less effective in bringing about this repression. Addition of either spermidine or spermine to the cells treated with the AdoMetDC inhibitors led to a decrease in ODC activity, indicating that either polyamine can bring about this effect, but spermidine produced effects at concentrations similar to those found in the control cells and appears to be the physiologically important regulator. The content of AdoMetDC protein (measured by radioimmunoassay) was also increased by these inhibitors, and a small increase in its mRNA content was observed, but this was insufficient to account for the increase in protein. A substantial stabilization of AdoMetDC occurred in these cells, contributing to the increased enzyme content, but an increase in the rate of translation cannot be ruled out./p
机译:>用两种S-腺苷甲硫氨酸脱羧酶抑制剂(AdoMetDC),即5'-脱氧-5'-[N-甲基-N- [2-(氨基-氧)乙基])氨基腺苷处理L1210细胞5'-脱氧-5'-[N-甲基-N-(3-肼基丙基)]氨基腺苷使鸟氨酸脱羧酶(ODC)蛋白的量大大增加。酶含量的增加归因于蛋白质降解速率的降低和合成速率的提高,但其mRNA含量没有变化。抑制剂导致细胞内亚精胺和亚精胺的量大量减少,但腐胺的量大量增加。这些结果表明,ODC的含量在蛋白质翻译和周转的水平上受亚精胺和亚精胺的负调控,但腐胺在产生这种抑制作用方面效果不佳。在用AdoMetDC抑制剂处理过的细胞中加入亚精胺或亚精胺会导致ODC活性降低,这表明任一多胺都可能导致这种作用,但亚精胺在与对照细胞类似的浓度下仍会产生作用。生理上重要的调节剂。这些抑制剂还增加了AdoMetDC蛋白的含量(通过放射免疫测定法测定),并且观察到其mRNA含量略有增加,但这不足以说明蛋白的增加。这些细胞中发生了AdoMetDC的基本稳定,这有助于增加酶的含量,但不能排除翻译速率的提高。

著录项

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