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Frequency-modulated nuclear localization bursts coordinate gene regulation

机译:调频核定位脉冲协调基因调控

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摘要

In yeast, the transcription factor Crz1 is dephosphorylated and translocates into the nucleus in response to extracellular calcium. Using time-lapse microscopy, we found that Crz1 exhibited short bursts of nuclear localization (∼2 minutes) that occurred stochastically in individual cells and propagated to the expression of downstream genes. Strikingly, calcium concentration controlled the frequency, but not duration, of localization bursts. Using an analytic model, we found that this frequency modulation (FM) of bursts ensures proportional expression of multiple target genes across a wide dynamic range of expression levels, independent of promoter characteristics. We experimentally confirmed this theory with natural and synthetic Crz1 target promoters. Another stress response transcription factor, Msn2, exhibits similar, but largely uncorrelated, localization bursts under calcium stress. These results suggest that FM regulation of localization bursts may be a general control strategy utilized by the cell to coordinate multi-gene responses to external signals.
机译:在酵母中,转录因子Crz1被去磷酸化并响应细胞外钙而转运到细胞核中。使用延时显微镜,我们发现Crz1表现出短暂的核定位爆发(约2分钟),在单个细胞中随机发生并传播到下游基因的表达。令人惊讶的是,钙浓度控制着定位爆发的频率,而不是持续时间。使用分析模型,我们发现这种突发频率调制(FM)可以确保多个目标基因在表达水平的广泛动态范围内成比例表达,而与启动子特征无关。我们用天然和合成的Crz1目标启动子实验证实了这一理论。另一个胁迫反应转录因子Msn2在钙胁迫下表现出相似但基本不相关的定位爆发。这些结果表明,定位脉冲的FM调节可能是细胞用来协调多基因对外部信号响应的一般控制策略。

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