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古德温模型:模拟放线菌酮和热休克对粗糙脉孢菌孢子形成节律的影响。

The Goodwin model: simulating the effect of cycloheximide and heat shock on the sporulation rhythm of Neurospora crassa.

作者信息

Ruoff P, Vinsjevik M, Mohsenzadeh S, Rensing L

机构信息

School of Technology and Science, Stavanger College, P.O. Box 2557 Ullandhaug, N-4004 Stavanger, Norway.

出版信息

J Theor Biol. 1999 Feb 21;196(4):483-94. doi: 10.1006/jtbi.1998.0846.

Abstract

The Goodwin model is a negative feedback oscillator which describes rather closely the putative molecular mechanism of the circadian clock of Neurospora and Drosophila. An essential feature is that one or two clock proteins are synthesized and degraded in a rhythmic fashion. When protein synthesis in N. crassa (wild-type frq+and long-period mutant frq7) was inhibited by continuous incubation with increasing concentrations of cycloheximide (CHX) the period of the circadian sporulation rhythmicity is only slightly increased. The explanation of this effect may be seen in the inhibition of protein synthesis and protein degradation. In the model, increasing inhibition of both processes led to very similar results with respect to period length. That protein degradation is, in fact, inhibited by CHX is shown by determining protein degradation in N. crassa by means of pulse chase experiments. Phase response curves (PRCs) of the N. crassa sporulation rhythm toward CHX which were reported in the literature and investigated in this paper revealed significant differences between frq+and the long period mutants frq7and csp -1 frq7. These PRCs were also convincingly simulated by the model, if a transient inhibition of protein degradation by CHX is assumed as well as a lower constitutive degradation rate of FRQ-protein in the frq7/ csp -1 frq7mutants. The lower sensitivities of frq7and csp -1 frq7towards CHX may thus be explained by a lower degradation rate of clock protein FRQ7. The phase shifting by moderate temperature pulses (from 25 to 30 degrees C) can also be simulated by the Goodwin model and shows large phase advances at about CT 16-20 as observed in experiments. In case of higher temperature pulses (from 35 to 42 or 45 degrees C=heat shock) the phase position and form of the PRC changes as protein synthesis is increasingly inhibited. It is known from earlier experiments that heat shock not only inhibits the synthesis of many proteins but also inhibits protein degradation. Taking this into account, the Goodwin model also simulates the PRCs of high temperature (heat shock) pulses.

摘要

古德温模型是一种负反馈振荡器,它相当精确地描述了粗糙脉孢菌和果蝇生物钟的假定分子机制。一个基本特征是一种或两种生物钟蛋白以有节奏的方式合成和降解。当用浓度不断增加的环己酰亚胺(CHX)持续孵育抑制粗糙脉孢菌(野生型frq +和长周期突变体frq7)中的蛋白质合成时,昼夜孢子形成节律的周期仅略有增加。这种效应的解释可能在于蛋白质合成和蛋白质降解的抑制。在该模型中,这两个过程抑制作用的增强在周期长度方面导致了非常相似的结果。通过脉冲追踪实验测定粗糙脉孢菌中的蛋白质降解表明,CHX实际上抑制了蛋白质降解。文献中报道并在本文中研究的粗糙脉孢菌孢子形成节律对CHX的相位响应曲线(PRC)揭示了frq +与长周期突变体frq7和csp -1 frq7之间的显著差异。如果假定CHX对蛋白质降解有短暂抑制作用,并且frq7 / csp -1 frq7突变体中FRQ蛋白的组成型降解速率较低,那么该模型也能令人信服地模拟这些PRC。因此,frq7和csp -1 frq7对CHX较低的敏感性可能是由于生物钟蛋白FRQ7的降解速率较低。适度温度脉冲(从25摄氏度到30摄氏度)引起的相位移动也可以用古德温模型模拟,并且如实验中所观察到的,在大约CT 16 - 20时显示出大的相位提前。在更高温度脉冲(从35摄氏度到42或45摄氏度 = 热休克)的情况下,随着蛋白质合成受到越来越多的抑制,PRC的相位位置和形式会发生变化。从早期实验中已知,热休克不仅抑制许多蛋白质的合成,还抑制蛋白质降解。考虑到这一点,古德温模型也能模拟高温(热休克)脉冲的PRC。

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