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翻译起始的替代方式和特定时间的磷酸化作用产生了基本生物钟蛋白频率的多种形式。

Alternative initiation of translation and time-specific phosphorylation yield multiple forms of the essential clock protein FREQUENCY.

作者信息

Garceau N Y, Liu Y, Loros J J, Dunlap J C

机构信息

Department of Biochemistry, Dartmouth Medical School, Hanover, New Hampshire 03755-3844, USA.

出版信息

Cell. 1997 May 2;89(3):469-76. doi: 10.1016/s0092-8674(00)80227-5.

Abstract

The frequency (frq) gene encodes central components of the transcription/translation-based negative-feedback loop comprising the core of the Neurospora circadian oscillator; posttranscriptional regulation associated with FRQ is surprisingly complex. Alternative use of translation initiation sites gives rise to two forms of FRQ whose levels peak 4-6 hr following the peak of frq transcript. Each form of FRQ is progressively phosphorylated over the course of the day, thus providing a number of temporally distinct FRQ products. The kinetics of these regulatory processes suggest a view of the clock where relatively rapid events involving translational regulation in the synthesis of FRQ and negative feedback of FRQ on frq transcript levels are followed by slower posttranslational regulation, ultimately driving the turnover of FRQ and reactivation of the frq gene.

摘要

频率(frq)基因编码基于转录/翻译的负反馈环的核心组件,该负反馈环构成了粗糙脉孢菌生物钟振荡器的核心;与FRQ相关的转录后调控惊人地复杂。翻译起始位点的交替使用产生了两种形式的FRQ,其水平在frq转录本峰值后4 - 6小时达到峰值。每种形式的FRQ在一天中会逐渐被磷酸化,从而产生许多时间上不同的FRQ产物。这些调控过程的动力学表明,在生物钟中,先是在FRQ合成过程中涉及翻译调控以及FRQ对frq转录本水平的负反馈等相对快速的事件,随后是较慢的翻译后调控,最终推动FRQ的周转和frq基因的重新激活。

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