Chen K Y, Canellakis E S
Proc Natl Acad Sci U S A. 1977 Sep;74(9):3791-5. doi: 10.1073/pnas.74.9.3791.
L-Asparagine is necessary and sufficient for the maximal induction of ornithine decarboxylase (ODC) (L-ornithine carboxy-lyase, EC 4.1.1.17) activity in confluent N18 mouse neuroblastoma cells in a salts/glucose medium; L-asparagine also induces maximal ODC activity when added to a tissue culture medium. L-Glutamine is about one-half as effective as asparagine. Cholera toxin and agents that are known to raise intracellular cyclic AMP concentrations have no effect on the induction of ODC activity unless suboptimal concentrations of asparagine are present in the salts/glucose medium. Whereas actinomycin D does not inhibit induction of ODC activity by asparagine, it inhibits the induction of ODC activity in association with cyclic AMP. In the salts/glucose medium, the rate of loss of ODC activity following the inhibition of protein synthesis by cycloheximide or puromycin depends upon the presence or absence of asparagine; loss is rapid only in the absence of asparagine and does not appear to be related to the inhibition of protein synthesis. These results are discussed in the context that the overlay of the growth medium tends to mask the minimal requirements for enzyme induction, because the composition of the medium defines: (a) the requirements for the induction of ODC activity; (b) the effect, or lack of effect, of cyclic AMP (and of inducers of intracellular cyclic AMP) on the induction of ODC activity; (c) the effect, or lack of effect, of actinomycin D on the induction of ODC activity; and (d) the action of puromycin and of cycloheximide on the rate of loss of ODC activity. It will be interesting to determine whether these results are uniquely applicable to ODC, whether many of the reactions attributed to cyclic AMP in the literature may be mediated by asparagine and glutamine, and whether actinomycin D, cycloheximide, and puromycin can be relied upon to differentiate between transcriptional and post-transcriptional control.
在盐/葡萄糖培养基中,L-天冬酰胺对于汇合状态的N18小鼠神经母细胞瘤细胞中鸟氨酸脱羧酶(ODC,L-鸟氨酸羧基裂解酶,EC 4.1.1.17)活性的最大诱导是必需且充分的;当添加到组织培养基中时,L-天冬酰胺也能诱导最大的ODC活性。L-谷氨酰胺的效力约为天冬酰胺的一半。霍乱毒素和已知能提高细胞内环状AMP浓度的试剂,除非盐/葡萄糖培养基中存在次优浓度的天冬酰胺,否则对ODC活性的诱导没有影响。虽然放线菌素D不抑制天冬酰胺对ODC活性的诱导,但它抑制与环状AMP相关的ODC活性诱导。在盐/葡萄糖培养基中,用环己酰亚胺或嘌呤霉素抑制蛋白质合成后ODC活性的丧失速率取决于天冬酰胺的存在与否;只有在没有天冬酰胺的情况下丧失才迅速,且这似乎与蛋白质合成抑制无关。这些结果是在生长培养基的覆盖往往会掩盖酶诱导的最低需求这一背景下进行讨论的,因为培养基的组成决定了:(a)ODC活性诱导的需求;(b)环状AMP(以及细胞内环状AMP诱导剂)对ODC活性诱导的影响或无影响;(c)放线菌素D对ODC活性诱导的影响或无影响;以及(d)嘌呤霉素和环己酰亚胺对ODC活性丧失速率的作用。确定这些结果是否仅适用于ODC、文献中许多归因于环状AMP的反应是否可能由天冬酰胺和谷氨酰胺介导,以及是否可以依靠放线菌素D、环己酰亚胺和嘌呤霉素来区分转录控制和转录后控制,将是很有趣的。