Palen E, Traugh J A
J Biol Chem. 1987 Mar 15;262(8):3518-23.
The effects of phosphorylation of ribosomal protein S6 by two different protein kinases, the cAMP-dependent protein kinase and the mitogen-stimulated S6 kinase, or translation of globin mRNA in a reconstituted system and on binding of globin mRNA to 40 S ribosomal subunits were examined. The cAMP-dependent protein kinase incorporated 1.5 mol of phosphate/mol of 40 S ribosomal subunits. Phosphorylation of S6 by the cAMP-dependent protein kinase had no effect on binding of 3' terminus-labeled globin mRNA to 40 S ribosomal subunits. [3H]Leucine incorporation with 40 S ribosomal subunits phosphorylated by the cAMP-dependent protein kinase was identical to that observed with nonphosphorylated 40 S ribosomal subunits, although on occasion, a slight inhibition (less than 10%) was observed; there was no effect on the rate of synthesis of either the alpha or beta chains of globin. Phosphorylation with the mitogen-stimulated S6 kinase (2.5 mol/mol) did not alter binding of globin mRNA to 40 S ribosomal subunits; however, translation of globin mRNA in the reconstituted protein-synthesizing system was stimulated up to 4-fold over that observed with nonphosphorylated subunits. Synthesis of both the alpha and beta chains of globin was enhanced by phosphorylation as shown by electrophoretic analysis. Since the sites phosphorylated by the mitogen-stimulated S6 kinase are identical to those observed in vivo in response to insulin and growth-promoting compounds, the data support the hypothesis that enhanced synthesis of specific proteins may be due to phosphorylation of S6 and that differential phosphorylation of S6 can alter translation of natural mRNA.
研究了两种不同的蛋白激酶,即环磷酸腺苷(cAMP)依赖性蛋白激酶和有丝分裂原刺激的S6激酶,对核糖体蛋白S6磷酸化的作用,以及在重组系统中对珠蛋白mRNA翻译的影响,还有对珠蛋白mRNA与40S核糖体亚基结合的影响。cAMP依赖性蛋白激酶每摩尔40S核糖体亚基掺入1.5摩尔磷酸盐。cAMP依赖性蛋白激酶对S6的磷酸化对3'末端标记的珠蛋白mRNA与40S核糖体亚基的结合没有影响。用cAMP依赖性蛋白激酶磷酸化的40S核糖体亚基掺入[3H]亮氨酸的情况与未磷酸化的40S核糖体亚基相同,不过偶尔会观察到轻微抑制(小于10%);对珠蛋白的α链或β链的合成速率没有影响。有丝分裂原刺激的S6激酶(2.5摩尔/摩尔)进行的磷酸化并没有改变珠蛋白mRNA与40S核糖体亚基的结合;然而,在重组的蛋白质合成系统中,珠蛋白mRNA的翻译比未磷酸化的亚基刺激高达4倍。电泳分析表明,珠蛋白的α链和β链的合成都因磷酸化而增强。由于有丝分裂原刺激的S6激酶磷酸化的位点与体内对胰岛素和促生长化合物反应时观察到的位点相同,这些数据支持这样的假说,即特定蛋白质合成的增强可能是由于S6的磷酸化,并且S6的差异磷酸化可以改变天然mRNA的翻译。