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A developmental cycle masks output from the circadian oscillator under conditions of choline deficiency in Neurospora

机译:一个发育周期掩盖了神经孢子虫胆碱缺乏条件下昼夜节律振荡器的输出

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In Neurospora, metabolic oscillators coexist with the circadian tran-scriptional/translational feedback loop governed by the FRQ (Frequency) and WC (White Collar) proteins. One of these, a choline deficiency oscillator (CDO) observed in chol-1 mutants grown under choline starvation, drives an uncompensated long-period developmental cycle (≈60-120 h). To assess possible contributions of this metabolic oscillator to the circadian system, molecular and physiological rhythms were followed in liquid culture under choline starvation, but these only confirmed that an oscillator with a normal circadian period length can run under choline starvation. This finding suggested that long-period developmental cycles elicited by nutritional stress could be masking output from the circadian system, although a caveat was that the CDO sometimes requires several days to become consolidated. To circumvent this and observe both oscillators simultaneously, we used an assay using a codon-optimized luciferase to follow the circadian oscillator. Under conditions where the long-period, uncompensated, CDO-driven developmental rhythm was expressed for weeks in growth tubes, the luciferase rhythm in the same cultures continued in a typical compensated manner with a circadian period length dependent on the allelic state of frq. Perio-dograms revealed no influence of the CDO on the circadian oscillator. Instead, the CDO appears as a cryptic metabolic oscillator that can, under appropriate conditions, assume control of growth and development, thereby masking output from the circadian system. frq-driven luciferase as a reporter of the circadian oscillator may in this way provide a means for assessing prospective role(s) of metabolic and/or ancillary oscillators within cellular circadian systems.
机译:在Neurospora中,代谢振荡器与由FRQ(频率)和WC(白领)蛋白控制的昼夜转录/翻译反馈回路共存。其中之一,是在胆碱饥饿下生长的chol-1突变体中观察到的胆碱缺乏振荡器(CDO),驱动了无补偿的长期发育周期(≈60-120h)。为了评估这种代谢振荡器对昼夜节律系统的可能贡献,在胆碱饥饿的液体培养中跟踪分子和生理节律,但是这些仅证实具有正常昼夜节律周期长度的振荡器可以在胆碱饥饿下运行。这一发现表明,营养压力引发的长期发育周期可能掩盖了昼夜节律系统的输出,尽管一个警告是,CDO有时需要几天才能被巩固。为了避免这种情况并同时观察两个振荡器,我们使用了一种采用密码子优化的荧光素酶的分析方法来跟踪昼夜节律振荡器。在生长管中持续表达数周的,无补偿的,由CDO驱动的发育节律的情况下,相同培养物中的萤光素酶节律以典型的补偿方式持续进行,其昼夜节律周期的长短取决于frq的等位基因状态。周期图显示CDO对昼夜节律振荡器没有影响。取而代之的是,CDO表现为一种隐秘的代谢振荡器,可以在适当的条件下控制生长发育,从而掩盖了昼夜节律系统的输出。 frq驱动的荧光素酶作为昼夜节律振荡器的报告子可以以此方式提供用于评估细胞昼夜节律系统内代谢和/或辅助振荡器的预期作用的手段。

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