Circadian rhythms, metabolic oscillators, and the target of rapamycin (TOR) pathway: the Neurospora connection

被引:8
|
作者
Lakin-Thomas, Patricia [1 ]
机构
[1] York Univ, Dept Biol, Toronto, ON M3J 1P3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Circadian; Metabolism; Neurospora crassa; Target of rapamycin; Oscillator; GENE-EXPRESSION; CHOLINE DEPLETION; CLOCK; CRASSA; TRANSCRIPTION; COMPENSATION; ENTRAINMENT; CYCLES; MTOR; MUTATIONS;
D O I
10.1007/s00294-018-0897-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Circadian (24-h) rhythmicity is a fundamental property of eukaryotic cells, and it is not surprising that it intersects with fundamental metabolic processes. Many links between these two processes have been documented, and speculation has been growing that there may be circadian metabolic oscillators that interact with and exist independently of the well-known circadian transcription/translation feedback loops (TTFLs) that have been extensively studied. This review takes a critical look at the evidence for the existence of metabolic oscillators at the cellular level, attempting to answer these questions: does metabolism affect circadian rhythmicity, and vice versa? Is metabolism rhythmic, and if so, is that rhythmicity cell autonomous? Systems displaying non-canonical rhythmicity in the absence of functional TTFLs provide opportunities for identifying metabolic oscillators, and this review emphasizes the fungus Neurospora crassa as a model system. Recent papers describing links between the target of rapamycin (TOR) signaling pathway and circadian rhythmicity are highlighted, suggesting the potential for TOR signaling in generating rhythmicity independent of TTFLs.
引用
收藏
页码:339 / 349
页数:11
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