Shi Mi, Larrondo Luis F, Loros Jennifer J, Dunlap Jay C
Departments of Genetics and Biochemistry, Dartmouth Medical School, Hanover, NH 03755, USA.
Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):20102-7. doi: 10.1073/pnas.0706631104. Epub 2007 Dec 4.
In Neurospora, metabolic oscillators coexist with the circadian transcriptional/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 ( approximately 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. Periodograms 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.
在粗糙脉孢菌中,代谢振荡器与由FRQ(频率)和WC(白领)蛋白控制的昼夜节律转录/翻译反馈环共存。其中之一是在胆碱饥饿条件下生长的胆碱营养缺陷型突变体中观察到的胆碱缺乏振荡器(CDO),它驱动一个无补偿的长周期发育循环(约60 - 120小时)。为了评估这种代谢振荡器对昼夜节律系统的可能贡献,在胆碱饥饿条件下对液体培养中的分子和生理节律进行了跟踪,但这些仅证实了具有正常昼夜节律周期长度的振荡器可以在胆碱饥饿条件下运行。这一发现表明,营养应激引发的长周期发育循环可能掩盖了昼夜节律系统的输出,不过需要注意的是,CDO有时需要几天时间才能巩固。为了规避这一点并同时观察两个振荡器,我们使用了一种检测方法,利用密码子优化的荧光素酶来跟踪昼夜节律振荡器。在生长管中长周期、无补偿、由CDO驱动的发育节律持续数周的条件下,同一培养物中的荧光素酶节律以典型的补偿方式继续,其昼夜节律周期长度取决于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。相反,CDO表现为一种隐蔽的代谢振荡器,在适当条件下可以控制生长和发育,从而掩盖昼夜节律系统的输出。以frq驱动的荧光素酶作为昼夜节律振荡器的报告基因,可能以此提供一种手段来评估细胞昼夜节律系统中代谢和/或辅助振荡器的潜在作用。