The Arabidopsis Framework Model version 2 predicts the organism-level effects of circadian clock gene mis-regulation

Author:

Chew Yin Hoon1ORCID,Seaton Daniel D1ORCID,Mengin Virginie2ORCID,Flis Anna2ORCID,Mugford Sam T3ORCID,George Gavin M4ORCID,Moulin Michael5,Hume Alastair6ORCID,Zeeman Samuel C4ORCID,Fitzpatrick Teresa B5ORCID,Smith Alison M3ORCID,Stitt Mark2ORCID,Millar Andrew J1ORCID

Affiliation:

1. SynthSys and School of Biological Sciences, C. H. Waddington Building, University of Edinburgh , King’s Buildings, Edinburgh EH9 3BF , UK

2. Max Planck Institute of Molecular Plant Physiology , Am Muehlenberg 1, 14476 Potsdam-Golm , Germany

3. Department of Metabolic Biology, John Innes Centre , Norwich NR4 7UH , UK

4. Institute of Molecular Plant Biology, ETH , Zurich , Switzerland

5. Department of Botany and Plant Biology, University of Geneva , Geneva , Switzerland

6. SynthSys and EPCC, Bayes Centre, University of Edinburgh , 47 Potterrow, Edinburgh EH8 9BT , UK

Abstract

Abstract Predicting a multicellular organism’s phenotype quantitatively from its genotype is challenging, as genetic effects must propagate across scales. Circadian clocks are intracellular regulators that control temporal gene expression patterns and hence metabolism, physiology and behaviour. Here we explain and predict canonical phenotypes of circadian timing in a multicellular, model organism. We used diverse metabolic and physiological data to combine and extend mathematical models of rhythmic gene expression, photoperiod-dependent flowering, elongation growth and starch metabolism within a Framework Model for the vegetative growth of Arabidopsis thaliana, sharing the model and data files in a structured, public resource. The calibrated model predicted the effect of altered circadian timing upon each particular phenotype in clock-mutant plants under standard laboratory conditions. Altered night-time metabolism of stored starch accounted for most of the decrease in whole-plant biomass, as previously proposed. Mobilization of a secondary store of malate and fumarate was also mis-regulated, accounting for any remaining biomass defect. The three candidate mechanisms tested did not explain this organic acid accumulation. Our results link genotype through specific processes to higher-level phenotypes, formalizing our understanding of a subtle, pleiotropic syndrome at the whole-organism level, and validating the systems approach to understand complex traits starting from intracellular circuits.

Funder

European Commission

BBSRC FLIP

BBSRC Institute Strategic Programme

Swiss National Science Foundation

University of Geneva

Zürich–Basel Plant Science Centre Plant Fellows Programme

Marie Skłodowska-Curie

ETH Zurich

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Agronomy and Crop Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Modeling and Simulation

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3