Cell biology: Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage

Science

Volumn 309, Issue 5734, 2005, Pages 630-633

  Dodd, Antony N ^a   Salathia, Neeraj ^b,d   Hall, Anthony ^b,e   Kévei, Eva ^c   Tóth, Réka ^c   Nagy, Ferenc ^c   Hibberd, Julian M ^a   Millar, Andrew J ^b,f   Webb, Alex A R ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF WARWICK   (United Kingdom)

^c INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^d HARVARD UNIVERSITY   (United States)

^e UNIVERSITY OF LIVERPOOL   (United Kingdom)

^f UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CHLOROPHYLL; CYTOLOGY; MUTAGENS; PHOTOSYNTHESIS;

CELL BIOLOGY; CIRCADIAN CLOCKS; CIRCADIAN CONTROLS; PLANT GROWTH;

PLANTS (BOTANY);

CHLOROPHYLL; ARABIDOPSIS PROTEIN; CARBON DIOXIDE; CCA1 PROTEIN, ARABIDOPSIS; TOC1 PROTEIN, ARABIDOPSIS; TRANSCRIPTION FACTOR;

CYTOLOGY;

ARABIDOPSIS; ARTICLE; CIRCADIAN RHYTHM; ENVIRONMENTAL FACTOR; LIGHT DARK CYCLE; NONHUMAN; PERIODICITY; PHOTOSYNTHESIS; PLANT GROWTH; PRIORITY JOURNAL; SURVIVAL RATE; BIOLOGICAL RHYTHM; BIOMASS; DARKNESS; GENE EXPRESSION REGULATION; GENETICS; GENOTYPE; GROWTH, DEVELOPMENT AND AGING; LIGHT; METABOLISM; MUTATION; PHYSIOLOGY; PLANT LEAF; PLANT SEED;

ARABIDOPSIS; ARABIDOPSIS THALIANA;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; BIOLOGICAL CLOCKS; BIOMASS; CARBON DIOXIDE; CHLOROPHYLL; CIRCADIAN RHYTHM; DARKNESS; GENE EXPRESSION REGULATION, PLANT; GENOTYPE; LIGHT; MUTATION; PHOTOSYNTHESIS; PLANT LEAVES; SEEDS; TRANSCRIPTION FACTORS;

EID: 22744451756     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1115581     Document Type: Article

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32. Authors E.K., R.T., A.H., and A.J.M. identified ztl-27; N.S. and A.J.M. conceived and performed competition and seedset experiments with A.H.; A.N.D., J.M.H., and A.A.R.W. performed all other experiments. We thank the U.K. Biotechnology and Biological Sciences Research Council (A.A.R.W., J.M.H., and A.J.M.); the Royal Society of London and the Isaac Newton Trust (A.A.R.W.); and the Howard Hughes Medical Institute (F.N.). We are grateful to E. Tobin (UCLA) and S. Kay (Scripps) for collaboration and donation of CCA1-OX and toc1-2, respectively.