Stoecklin G, Hahn S, Moroni C
Institute for Medical Microbiology, University of Basel, Switzerland.
J Biol Chem. 1994 Nov 18;269(46):28591-7.
In mast cells, expression of interleukin-3 (IL-3) is induced following IgE-receptor activation via calcium-dependent mRNA stabilization. We performed a mutational analysis of the 8 AUUUA motifs located in the 3'-untranslated region of IL-3 mRNA, and analyzed the effect on mRNA stability in PB-3c mast cells. Similar to endogenous IL-3 mRNA, exogenous IL-3 transcripts had a short half-life and were stabilized following stimulation of calcium influx by ionomycin. Specific mutation of 3 AUUUA motifs had almost the same stabilizing effect as deletion of the entire AU-rich region. Mutating even a single critical motif led to a weak, but significant mRNA stabilization. Ionomycin treatment did not further enhance the expression of mutationally stabilized transcripts. Our data fit a model, where within a cluster of 6 AUUUA motifs, 3 adjacent motifs are required for binding of a factor which mediates rapid IL-3 mRNA decay. Activity of such a factor might be under control of a calcium-dependent pathway.
在肥大细胞中,白细胞介素-3(IL-3)的表达是在IgE受体通过钙依赖性mRNA稳定化激活后诱导产生的。我们对位于IL-3 mRNA 3'非翻译区的8个AUUUA基序进行了突变分析,并分析了其对PB-3c肥大细胞中mRNA稳定性的影响。与内源性IL-3 mRNA相似,外源性IL-3转录本半衰期较短,在离子霉素刺激钙内流后被稳定化。3个AUUUA基序的特异性突变与整个富含AU区域的缺失具有几乎相同的稳定作用。即使单个关键基序发生突变也会导致mRNA有微弱但显著的稳定化。离子霉素处理并未进一步增强突变稳定化转录本的表达。我们的数据符合一个模型,即在6个AUUUA基序的簇中,3个相邻基序是介导IL-3 mRNA快速降解的因子结合所必需的。这种因子的活性可能受钙依赖性途径的控制。