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Light and clock expression of the Neurospora clock gene frequency is differentially driven by but dependent on WHITE COLLAR-2.

机译:Neurospora时钟基因频率的光和时钟表达受WHITE COLLAR-2的差异驱动但取决于WHITE COLLAR-2。

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摘要

Visible light is thought to reset the Neurospora circadian clock by acting through heterodimers of the WHITE COLLAR-1 and WHITE COLLAR-2 proteins to induce transcription of the frequency gene. To characterize this photic entrainment we examined frq expression in constant light, under which condition the mRNA and protein of this clock gene were strongly induced. In continuous illumination FRQ accumulated in a highly phosphorylated state similar to that seen at subjective dusk, the time at which a step from constant light to darkness sets the clock. Examination of frq expression in several wc-2 mutant alleles surprisingly revealed differential regulation when frq expression was compared between constant light, following a light pulse, and darkness (clock-driven expression). Construction of a wc-2 null strain then demonstrated that WC-2 is absolutely required for both light and clock-driven frq expression, in contrast to previous expectations based on presumptive nulls containing altered Zn-finger function. Additionally, we found that frq light signal transduction differs from that of other light-regulated genes. Thus clock and light-driven frq expression is differentially regulated by, but dependent on, WC-2.
机译:人们认为可见光通过通过WHITE COLLAR-1和WHITE COLLAR-2蛋白的异二聚体起作用来重置Neurospora昼夜节律,从而诱导频率基因的转录。为了表征这种光合夹带,我们在恒定光照下检查了frq的表达,在这种情况下强烈诱导了该时钟基因的mRNA和蛋白质。在连续照明下,FRQ以高度磷酸化的状态积累,类似于在主观黄昏时看到的状态,从恒定的光照到黑暗的时间设置了时钟。当在恒定光(跟随光脉冲)和黑暗(时钟驱动的表达)之间比较frq表达时,在几个wc-2突变等位基因中对frq表达的检查令人惊讶地揭示了差异调节。然后建立一个wc-2无效菌株,证明光和时钟驱动的frq表达都绝对需要WC-2,这与以前基于含有改变的锌指功能的假定无效物质的预期相反。此外,我们发现frq光信号转导不同于其他光调节基因。因此,时钟和光驱动的frq表达受WC-2(但取决于WC-2)的调节。

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