Garmendia-Torres Cecilia, Goldbeter Albert, Jacquet Michel
Université de Paris-Sud, Unité Mixte de Recherche 8621, Centre National de la Recherche Scientifique, Orsay, F-91405, France.
Curr Biol. 2007 Jun 19;17(12):1044-9. doi: 10.1016/j.cub.2007.05.032.
At intermediate intensities, stress induces oscillations in the nucleocytoplasmic shuttling of the transcription factor Msn2 in budding yeast. Activation by stress results in a reversible translocation of Msn2 from the cytoplasm to the nucleus. This translocation is negatively controlled by the cAMP-PKA pathway through Msn2 phosphorylation. Here we show that the nuclear localization signal (NLS) of Msn2 is necessary and sufficient to promote the nucleocytoplasmic oscillations of the transcription factor. Because the NLS is controlled by protein kinase A (PKA) phosphorylation, we use a computational model to investigate the possibility that the cAMP-PKA pathway could function as an oscillator driving the periodic shuttling of Msn2. The model indicates that sustained oscillations of cAMP can indeed occur in a range bounded by two critical values of stress intensity, owing to the negative feedback exerted by PKA on cAMP accumulation. We verify the predictions of the model in mutants by showing that suppressing this negative-feedback loop prevents the oscillatory shuttling but still promotes the stress-induced nuclear localization of Msn2. The physiological significance of Msn2 oscillations is discussed in the light of the frequency encoding of cellular rhythms.
在中等强度下,应激会诱导出芽酵母中转录因子Msn2的核质穿梭振荡。应激激活会导致Msn2从细胞质可逆地转运到细胞核。这种转运受到cAMP-PKA途径通过Msn2磷酸化的负调控。在这里,我们表明Msn2的核定位信号(NLS)对于促进转录因子的核质振荡是必要且充分的。由于NLS受蛋白激酶A(PKA)磷酸化的控制,我们使用计算模型来研究cAMP-PKA途径是否可能作为驱动Msn2周期性穿梭的振荡器发挥作用。该模型表明,由于PKA对cAMP积累施加的负反馈,cAMP的持续振荡确实可以在由两个临界应激强度值界定的范围内发生。我们通过表明抑制这种负反馈回路可防止振荡穿梭,但仍促进应激诱导的Msn2核定位,来验证突变体中模型的预测。我们根据细胞节律的频率编码讨论了Msn2振荡的生理意义。