Minimal models of the circadian clock in a novel biological system
新型生物系统中生物钟的最小模型
基本信息
- 批准号:BB/F005466/1
- 负责人:
- 金额:$ 42.65万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2007
- 资助国家:英国
- 起止时间:2007 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Photosynthetic organisms are vital to our economy and survival, playing a critical role in the global carbon cycle and affecting the climate of our planet. Recent advances offer us the methods to understand the complex control of growth and activity in photosynthetic organisms. The 24-hour circadian clock is a key regulator in plants, and is also important in cyanobacteria, fungi and animals including humans. The UK teams have shown that rhythmic control of biological activity by the circadian clock increases growth and survival of Arabidopsis thaliana plants, probably because >15% of genes in Arabidopsis are clock-regulated. The Arabidopsis circadian clock is becoming a paradigm for systems biology. The clock mechanism is a small gene network with multiple feedback loops, comprising five pseudo-response regulators, three myb-related proteins, two F-box proteins, and additional plant-specific proteins. Millar's group has modelled a simplified Arabidopsis clock mechanism, with three interlocking feedback loops. Predictions of the models have been validated by new experiments, identifying an additional part of the clock network. This is still a rare achievement in any organism. Including the real complexity of the Arabidopsis clock, however, will greatly enlarge the models, making them more difficult to use and to understand. The dynamics of the clock system are complex. It can generate autonomous, 24-hour biological rhythms of gene expression but in nature the day/night cycle forces the system, resetting the clock. Light signals regulate four different components in the current clock model. In reality, these signals originate from at least eight photoreceptor proteins and probably control additional components. This complexity hampers circadian research in Arabidopsis. A simpler clock system that included only one of each protein type would enormously facilitate the experimental analysis of the clock mechanism. It would provide a natural test for the proposed benefits of complexity in the clock mechanism, giving general insight into other complex clocks for example in humans. If the whole organism were simple, it could reveal much more easily how correct timing of particular clock-regulated biochemical processes led to adaptive benefits. The French team has developed this ideal model. Ostreococcus tauri is the smallest free-living eukaryote, with a circadian system that is closely related to that of Arabidopsis. Crucially, each protein type is represented by only one gene in Ostreococcus. The Bouget lab has developed a unique set of experimental tools for functional genomics in this organism. Their recent results demonstrate that the Ostreococcus clock conserves the same mechanisms and gene interactions as the clock in Arabidopsis, but in a far simpler system. Modelling by the Lefranc group confirms that very simple mathematical models, which were invalidated by data in Arabidopsis, accurately describe the Ostreococcus clock. The world-leading results of the UK and French teams are naturally complementary, but in addition are supported by significant national and institutional investment on both sides. We are poised to make a major impact, gaining significant added value from these resources and opening up a new application area. We will combine the UK team's expertise in complex models, and the wealth of comparative data and models on Arabidopsis, with the French team's experimental system and expertise in nonlinear dynamics. Experimentally, we will generate biological materials to monitor and manipulate all the clock components in Ostreococcus, then use these materials to generate high-quality timeseries data for modelling. We will identify all clock-regulated transcripts and promoter sequences using RNA expression microarrays and promoter arrays. These results will form a case study for Plant Systems Biology, demonstrating the power of a unicellular system to accelerate understanding of core processes.
光合生物对我们的经济和生存至关重要,在全球碳循环中发挥关键作用,并影响我们星球的气候。最近的进展为我们提供了理解光合生物生长和活动的复杂控制的方法。24小时生物钟是植物的关键调节器,在蓝藻、真菌和包括人类在内的动物中也很重要。英国研究小组已经表明,生物钟对生物活动的节律控制增加了拟南芥植物的生长和存活,这可能是因为拟南芥中超过15%的基因是受时钟调节的。拟南芥生物钟正在成为系统生物学的一个范例。时钟机制是一个具有多个反馈回路的小基因网络,包括五个假反应调节因子,三个myb相关蛋白,两个F-box蛋白和其他植物特异性蛋白。Millar的研究小组已经建立了一个简化的拟南芥时钟机制模型,其中有三个互锁的反馈回路。新的实验验证了模型的预测,确定了时钟网络的额外部分。这在任何生物体中仍然是一个罕见的成就。然而,将拟南芥时钟的真实的复杂性包括在内,将大大扩大模型,使它们更难使用和理解。时钟系统的动态是复杂的。它可以产生自主的,24小时的基因表达生物节律,但在自然界中,昼夜循环迫使系统重置时钟。光信号调节当前时钟模型中的四个不同组件。事实上,这些信号至少来自八种感光蛋白,并可能控制其他成分。这种复杂性阻碍了拟南芥的昼夜节律研究。一个更简单的时钟系统,只包括每种蛋白质类型中的一种,将极大地促进时钟机制的实验分析。它将为时钟机制的复杂性的拟议好处提供一个自然的测试,从而对其他复杂的时钟(例如人类)提供一般的洞察力。如果整个生物体都是简单的,那么它就可以更容易地揭示特定生物钟调节的生化过程的正确时间如何导致适应性益处。法国团队开发了这种理想的模型。金牛牡蛎是最小的自由生活真核生物,其昼夜节律系统与拟南芥密切相关。至关重要的是,每种蛋白质类型在Ostreococcus中仅由一个基因代表。Bouget实验室开发了一套独特的实验工具,用于这种生物体的功能基因组学。他们最近的研究结果表明,Ostreococcus时钟与拟南芥中的时钟保持相同的机制和基因相互作用,但系统要简单得多。Lefranc小组的建模证实了非常简单的数学模型,这些模型被拟南芥中的数据所推翻,准确地描述了Ostreococcus时钟。英国和法国团队的世界领先成果自然是互补的,但除此之外,还得到了双方大量国家和机构投资的支持。我们准备发挥重大影响,从这些资源中获得显著的附加值,并开辟新的应用领域。我们将联合收割机结合英国团队在复杂模型方面的专业知识,以及拟南芥的大量比较数据和模型,以及法国团队在非线性动力学方面的实验系统和专业知识。在实验中,我们将生成生物材料来监控和操纵Ostreococcus中的所有时钟组件,然后使用这些材料生成高质量的时间序列数据进行建模。我们将使用RNA表达微阵列和启动子阵列鉴定所有的时钟调节转录本和启动子序列。这些结果将形成植物系统生物学的案例研究,展示单细胞系统加速理解核心过程的能力。
项目成果
期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Proteasome function is required for biological timing throughout the twenty-four hour cycle.
- DOI:10.1016/j.cub.2011.03.060
- 发表时间:2011-05-24
- 期刊:
- 影响因子:9.2
- 作者:van Ooijen, Gerben;Dixon, Laura E.;Troein, Carl;Millar, Andrew J.
- 通讯作者:Millar, Andrew J.
Multiple light inputs to a simple clock circuit allow complex biological rhythms.
- DOI:10.1111/j.1365-313x.2011.04489.x
- 发表时间:2011-04
- 期刊:
- 影响因子:0
- 作者:Troein C;Corellou F;Dixon LE;van Ooijen G;O'Neill JS;Bouget FY;Millar AJ
- 通讯作者:Millar AJ
Complementary approaches to understanding the plant circadian clock
- DOI:10.4204/eptcs.19.1
- 发表时间:2010-01-01
- 期刊:
- 影响因子:0
- 作者:Akman, Ozgur E.;Guerriero, Maria Luisa;Troein, Carl
- 通讯作者:Troein, Carl
Circadian rhythms persist without transcription in a eukaryote.
- DOI:10.1038/nature09654
- 发表时间:2011-01-27
- 期刊:
- 影响因子:64.8
- 作者:O'Neill, John S.;van Ooijen, Gerben;Dixon, Laura E.;Troein, Carl;Corellou, Florence;Bouget, Francois-Yves;Reddy, Akhilesh B.;Millar, Andrew J.
- 通讯作者:Millar, Andrew J.
Microarray data can predict diurnal changes of starch content in the picoalga Ostreococcus.
- DOI:10.1186/1752-0509-5-36
- 发表时间:2011-02-26
- 期刊:
- 影响因子:0
- 作者:Sorokina O;Corellou F;Dauvillée D;Sorokin A;Goryanin I;Ball S;Bouget FY;Millar AJ
- 通讯作者:Millar AJ
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Andrew Millar其他文献
Pompe Disease in the United Kingdom Compared with the Rest-of-World: Data from the Pompe Registry
- DOI:
10.1016/j.clinthera.2011.05.060 - 发表时间:
2011-06-01 - 期刊:
- 影响因子:
- 作者:
Mark E. Roberts;Simon Jones;Andrew Millar;Suyash Prasad; Pompe Registry Boards of Advisors - 通讯作者:
Pompe Registry Boards of Advisors
Combined analysis of studies of the effects of the matrix metalloproteinase inhibitor marimastat on serum tumor markers in advanced cancer: selection of a biologically active and tolerable dose for longer-term studies.
基质金属蛋白酶抑制剂马马司他对晚期癌症血清肿瘤标志物影响研究的联合分析:为长期研究选择生物活性和耐受剂量。
- DOI:
- 发表时间:
1998 - 期刊:
- 影响因子:11.5
- 作者:
J. Nemunaitis;Christopher Poole;J. Primrose;Alexander Rosemurgy;John Malfetano;Peter Brown;Amy Berrington;Alan Cornish;K. Lynch;H. Rasmussen;David Kerr;D. Cox;Andrew Millar - 通讯作者:
Andrew Millar
The Correspondence
- DOI:
10.1093/oseo/instance.00278955 - 发表时间:
2020-12 - 期刊:
- 影响因子:0
- 作者:
Andrew Millar - 通讯作者:
Andrew Millar
A Randomized Phase-II Study of BB-10010 (Macrophage Inflammatory Protein- 1α) in Patients With Advanced Breast Cancer Receiving 5-Fluorouracil, Adriamycin, and Cyclophosphamide Chemotherapy
- DOI:
10.1182/blood.v92.5.1532 - 发表时间:
1998-09-01 - 期刊:
- 影响因子:
- 作者:
Mark J. Clemons;Ernest Marshall;Jan Dürig;Ken Watanabe;Anthony Howell;David Miles;Helena Earl;Julie Kiernan;Audrey Griffiths;K. Towlson;P. DeTakats;Nydia G. Testa;Mark Dougal;Michael G. Hunter;L. Michael Wood;Lloyd G. Czaplewski;Andrew Millar;T. Michael Dexter;Brian I. Lord - 通讯作者:
Brian I. Lord
Su1825 Management of Gastric Intestinal Metaplasia in the UK: A Preliminary Survey
- DOI:
10.1016/s0016-5085(13)61790-4 - 发表时间:
2013-05-01 - 期刊:
- 影响因子:
- 作者:
Ratna Pandey;Andrew Millar - 通讯作者:
Andrew Millar
Andrew Millar的其他文献
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{{ truncateString('Andrew Millar', 18)}}的其他基金
The Parameter Optimisation Problem: Addressing a Key Challenge in Computational Systems Biology
参数优化问题:解决计算系统生物学的关键挑战
- 批准号:
EP/N018125/1 - 财政年份:2016
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
Bridging systems biology and advanced computing, to realise multi-scale biological modelling.
连接系统生物学和先进计算,实现多尺度生物建模。
- 批准号:
BB/M017605/1 - 财政年份:2015
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
Experimental methods and modelling for multiscale biology
多尺度生物学的实验方法和建模
- 批准号:
BB/N012348/1 - 财政年份:2015
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
US Partnering Award: Systems Biology of Plants and Algae, from Molecular Networks to Informatics Infrastructure.
美国合作奖:植物和藻类的系统生物学,从分子网络到信息学基础设施。
- 批准号:
BB/L026996/1 - 财政年份:2014
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
Does an ancient circadian clock control transcriptional rhythms using a non-transcriptional oscillator?
古代生物钟是否使用非转录振荡器控制转录节律?
- 批准号:
BB/J009423/1 - 财政年份:2012
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
A modelling portal for the UK plant systems biology community
英国植物系统生物学界的建模门户
- 批准号:
BB/F010583/1 - 财政年份:2008
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
Centre for Systems Biology at Edinburgh
爱丁堡系统生物学中心
- 批准号:
BB/D019621/1 - 财政年份:2007
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
Multiple light input signals to the gene network of the circadian clock
生物钟基因网络的多个光输入信号
- 批准号:
BB/E015263/1 - 财政年份:2007
- 资助金额:
$ 42.65万 - 项目类别:
Research Grant
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Circadian rhythm control of chronic pain and neuroinflammation: a bedside-to-bench study
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