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本文引用的文献

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Adaptive evolution of signaling partners.信号传导伙伴的适应性进化。
Mol Biol Evol. 2015 Apr;32(4):998-1007. doi: 10.1093/molbev/msu404. Epub 2015 Jan 6.
2
Reciprocal encoding of signal intensity and duration in a glucose-sensing circuit.葡萄糖感应回路中信号强度和持续时间的相互编码。
Cell. 2014 Feb 27;156(5):1084-95. doi: 10.1016/j.cell.2014.01.013.
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Endocytosis of the seven-transmembrane RGS1 protein activates G-protein-coupled signalling in Arabidopsis.七跨膜 RGS1 蛋白的内吞作用激活拟南芥中的 G 蛋白偶联信号转导。
Nat Cell Biol. 2012 Oct;14(10):1079-88. doi: 10.1038/ncb2568. Epub 2012 Sep 2.
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G protein activation without a GEF in the plant kingdom.植物王国中没有鸟苷酸交换因子的 G 蛋白激活。
PLoS Genet. 2012 Jun;8(6):e1002756. doi: 10.1371/journal.pgen.1002756. Epub 2012 Jun 28.
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Synthetic incoherent feedforward circuits show adaptation to the amount of their genetic template.合成非相干前馈电路表现出对其遗传模板数量的适应能力。
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T cell state transition produces an emergent change detector.T 细胞状态转变产生了一个新的变化探测器。
J Theor Biol. 2011 Apr 21;275(1):59-69. doi: 10.1016/j.jtbi.2011.01.031. Epub 2011 Jan 27.
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Glucose attenuation of auxin-mediated bimodality in lateral root formation is partly coupled by the heterotrimeric G protein complex.葡萄糖减弱了生长素介导的侧根形成中的双峰模式,这部分是由异三聚体 G 蛋白复合物耦合的。
PLoS One. 2010 Sep 17;5(9):e12833. doi: 10.1371/journal.pone.0012833.
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The control of the controller: molecular mechanisms for robust perfect adaptation and temperature compensation.控制器的调控:实现稳健完美适应和温度补偿的分子机制
Biophys J. 2009 Sep 2;97(5):1244-53. doi: 10.1016/j.bpj.2009.06.030.
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Defining network topologies that can achieve biochemical adaptation.定义能够实现生化适应的网络拓扑结构。
Cell. 2009 Aug 21;138(4):760-73. doi: 10.1016/j.cell.2009.06.013.
10
D-Glucose sensing by a plasma membrane regulator of G signaling protein, AtRGS1.通过G信号蛋白的质膜调节因子AtRGS1进行D-葡萄糖传感。
FEBS Lett. 2008 Oct 29;582(25-26):3577-84. doi: 10.1016/j.febslet.2008.08.038. Epub 2008 Sep 24.

一种用于光合作用效率的阴影探测器。

A shadow detector for photosynthesis efficiency.

作者信息

Liao Kang-Ling, Jones Roger D, McCarter Patrick, Tunc-Ozdemir Meral, Draper James A, Elston Timothy C, Kramer David, Jones Alan M

机构信息

Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Center for Complex Systems and Enterprises, Stevens Institute of Technology, Hoboken, NJ 07030, USA.

出版信息

J Theor Biol. 2017 Feb 7;414:231-244. doi: 10.1016/j.jtbi.2016.11.027. Epub 2016 Dec 3.

DOI:10.1016/j.jtbi.2016.11.027
PMID:27923735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5635846/
Abstract

Plants tolerate large variations in the intensity of the light environment by controlling the efficiency of solar to chemical energy conversion. To do this, plants have a mechanism to detect the intensity, duration, and change in light as they experience moving shadows, flickering light, and cloud cover. Sugars are the primary products of CO fixation, a metabolic pathway that is rate limited by this solar energy conversion. We propose that sugar is a signal encoding information about the intensity, duration and change in the light environment. We previously showed that the Arabidopsis heterotrimeric G protein complex including its receptor-like Regulator of G signaling protein, AtRGS1, detects both the concentration and the exposure time of sugars (Fu et al., 2014. Cell 156: 1084-1095). This unique property, designated dose-duration reciprocity, is a behavior that emerges from the system architecture / system motif. Here, we show that another property of the signaling system is to detect large changes in light while at the same time, filtering types of fluctuation in light that do not affect photosynthesis efficiency. When AtRGS1 is genetically ablated, photosynthesis efficiency is reduced in a changing- but not a constant-light environment. Mathematical modeling revealed that information about changes in the light environment is encoded in the amount of free AtRGS1 that becomes compartmentalized following stimulation. We propose that this property determines when to adjust photosynthetic efficiency in an environment where light intensity changes abruptly caused by moving shadows on top of a background of light changing gradually from sun rise to sun set and fluctuating light such as that caused by fluttering leaves.

摘要

植物通过控制太阳能到化学能的转换效率来耐受光照环境强度的大幅变化。为此,植物具有一种机制,可在经历移动阴影、闪烁光和云层覆盖时检测光的强度、持续时间和变化。糖类是二氧化碳固定的主要产物,这一代谢途径受太阳能转换的速率限制。我们提出,糖类是一种编码光照环境强度、持续时间和变化信息的信号。我们之前表明,拟南芥异源三聚体G蛋白复合物,包括其类受体G信号调节蛋白AtRGS1,可检测糖类的浓度和暴露时间(Fu等人,2014年。《细胞》156:1084 - 1095)。这种独特的特性,称为剂量 - 持续时间互易性,是一种从系统架构/系统基序中产生的行为。在这里,我们表明信号系统的另一个特性是检测光照的大幅变化,同时过滤不影响光合作用效率的光照波动类型。当AtRGS1基因被敲除时,在变化的光照环境而非恒定光照环境中,光合作用效率会降低。数学建模表明,光照环境变化的信息编码在刺激后被分隔的游离AtRGS1的量中。我们提出,这一特性决定了在由日出到日落逐渐变化的光照背景以及如树叶飘动引起的波动光照之上,因移动阴影导致光照强度突然变化的环境中,何时调整光合作用效率。