Starch and the clock: The dark side of plant productivity

Trends in Plant Science

Volumn 16, Issue 3, 2011, Pages 169-175

  Graf, Alexander ^a,b   Smith, Alison M ^a  

^a JOHN INNES CENTRE   (United Kingdom)

^b ETH ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS PROTEIN; CARBON; STARCH;

ARABIDOPSIS; CARBOHYDRATE METABOLISM; CIRCADIAN RHYTHM; DARKNESS; GENETICS; GROWTH, DEVELOPMENT AND AGING; LIGHT; METABOLISM; PHOTOPERIODICITY; PHOTOSYNTHESIS; PHYSIOLOGY; PLANT LEAF; REVIEW;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; CARBOHYDRATE METABOLISM; CARBON; CIRCADIAN CLOCKS; DARKNESS; LIGHT; PHOTOPERIOD; PHOTOSYNTHESIS; PLANT LEAVES; STARCH;

ARABIDOPSIS;

EID: 79952446665     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2010.12.003     Document Type: Review

References (49)

1. Dilkes N.B., et al. Temporal dynamics of carbon partitioning and rhizodeposition in wheat. Plant Physiol. 2004, 134:706-715.
2. Farrar J., et al. How roots control the flux of carbon to the rhizosphere. Ecology 2003, 84:827-837.
3. Peñuelas J., Staudt M. BVOCs and global change. Trends Plant Sci. 2010, 15:133-144.
4. 2 concentrations. Science 2006, 312:1918-1921.
5. 2. New Phytol. 2005, 165:351-371.
6. 2 effects on plant carbon, nitrogen, and water relations: six important lessons from FACE. J. Exp. Bot. 2009, 60:2859-2876.
7. Long S.P., et al. Can improvement in photosynthesis increase crop yields?. Plant Cell Env. 2006, 29:315-330.
8. Leakey A.D.B., et al. Genomic basis for stimulated respiration by plants growing under elevated carbon dioxide. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:3597-3602.
9. 2 increases root exudation from loblolly pine (Pinus taeda) seedlings as an N-mediated response. Tree Physiol. 2009, 29:1513-1523.
10. Long S.P., et al. Rising atmospheric carbon dioxide: plants face the future. Annu. Rev. Plant Biol. 2004, 55:591-628.
11. Zhu X.G., et al. Improving photosynthetic efficiency for greater yield. Annu. Rev. Plant Biol. 2010, 61:235-261.
12. Zeeman S.C., ap Rees T. Changes in carbohydrate metabolism and assimilate partitioning in starch excess mutants of Arabidopsis. Plant Cell Env. 1999, 22:1445-1453.
13. Smith A.M., Stitt M. Coordination of carbon supply and plant growth. Plant Cell Env. 2007, 30:1126-1149.
14. Wiese A., et al. Spatio-temporal leaf growth patterns of Arabidopsis thaliana and evidence for sugar control of the diel leaf growth cycle. New Phytol. 2007, 174:752-761.
15. Gibon Y., et al. Adjustment of diurnal starch turnover to short days: depletion of sugar during the night leads to a temporary inhibition of carbohydrate utilization, accumulation of sugars and post-translational activation of ADP-glucose pyrophosphorylase in the following light period. Plant J. 2004, 39:847-862.
16. Usadel B., et al. Global transcript levels respond to small changes of the carbon status during a progressive exhaustion of carbohydrates in Arabidopsis rosettes. Plant Physiol. 2008, 146:1834-1861.
17. Lu Y., et al. Daylength and circadian effects on starch degradation and maltose metabolism. Plant Physiol. 2005, 138:2280-2291.
18. Graf A., et al. Circadian control of carbohydrate availability for growth in Arabidopsis plants at night. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:9458-9463.
19. Harmer S.L. The circadian system in higher plants. Annu. Rev. Plant Biol. 2009, 60:357-377.
20. Covington M.F., et al. Global transcriptome analysis reveals circadian regulation of key pathways in plant growth and development. Genome Biol. 2008, 9:R130.
21. Fukushima A., et al. Impact of clock-associated Arabidopsis pseudo-response regulators in metabolic coordination. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:7251-7256.
22. Nakamichi N., et al. Linkage between circadian clock and tricarboxylic acid cycle in Arabidopsis. Plant Signal. Behav. 2009, 4:660-662.
23. Khan S., et al. Coordination of the maize transcriptome by a conserved circadian clock. BMC Plant Biol. 2010, 10:576-584.
24. Alabadi D., et al. Reciprocal regulation between TOC1 and LHY/CCA1 within the Arabidopsis circadian clock. Science 2001, 293:880-883.
25. Locke J.C., et al. Extension of a genetic network model by iterative experimentation and mathematical analysis. Mol. Syst. Biol. 2005, 1. 2005.0013.
26. Mizoguchi T., et al. LHY and CCA1 are partially redundant genes required to maintain circadian rhythms in Arabidopsis. Dev. Cell 2002, 2:629-641.
27. Chia T., et al. A cytosolic glucosyltransferase is required for conversion of starch to sucrose in Arabidopsis leaves at night. Plant J. 2004, 37:853-863.
28. Smith S.M., et al. Diurnal changes in the transcriptome encoding enzymes of starch metabolism provide evidence for both transcriptional and posttranscriptional regulation of starch metabolism in Arabidopsis leaves. Plant Physiol. 2004, 136:2687-2699.
29. Yu T.S., et al. The Arabidopsis sex1 mutant is defective in the R1 protein, a general regulator of starch degradation in plants, and not in the chloroplast hexose transporter. Plant Cell 2001, 13:1907-1918.
30. Mikkelsen R., et al. Alpha-glucan, water dikinase (GWD): a plastidic enzyme with redox-regulated and coordinated catalytic activity and binding affinity. Proc. Natl. Acad. Sci. U. S. A. 2005, 102:1785-1790.
31. Sokolov L.N., et al. A redox-regulated chloroplast protein phosphatase binds to starch diurnally and functions in its accumulation. Proc. Natl. Acad. Sci. U. S. A. 2006, 103:9732-9737.
32. Sparla F., et al. Redox regulation of a novel plastid-targeted beta-amylase of Arabidopsis. Plant Physiol. 2006, 141:840-850.
33. Dodd A.N., et al. Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage. Science 2005, 309:630-633.
34. Ni Z., et al. Altered circadian rhythms regulate growth vigour in hybrids and allopolyploids. Nature 2008, 457:327-331.
35. Zeeman S.C., et al. Starch: Its metabolism, evolution, and biotechnological modification in plants. Annu. Rev. Plant Biol. 2010, 61:209-234.
36. Sulpice R., et al. Starch as a major integrator in the regulation of plant growth. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:10348-10353.
37. Gibon Y., et al. Adjustment of growth, starch turnover, protein content and central metabolism to a decrease of the carbon supply when Arabidopsis is grown in very short photoperiods. Plant Cell Env. 2009, 32:859-874.
38. Piques M., et al. Ribosome and transcript copy numbers, polysome occupancy and enzyme dynamics in Arabidopsis. Mol. Syst. Biol. 2009, 5:314.
39. Stitt M., et al. Arabidopsis and primary photosynthetic metabolism - more than the icing on the cake. Plant J. 2010, 61:1067-1091.
40. Cross J.M., et al. Variation of enzyme activities and metabolite levels in 24 Arabidopsis accessions growing in carbon-limited conditions. Plant Physiol. 2006, 142:1574-1588.
41. Chatterton N.J., Silvius J.E. Photosynthate partitioning into starch in soybean leaves. I. Effects of photoperiod versus photosynthetic period duration. Plant Physiol. 1979, 64:749-753.
42. Lorenzen J.H., Ewing E.E. Starch accumulation in leaves of potato (Solanum tuberosum L.) during the first 18 days of photoperiod treatment. Ann. Bot. 1992, 69:481-485.
43. Fondy B.R., Geiger D.R. Diurnal pattern of translocation and carbohydrate metabolism in source leaves of Beta vulgaris L. Plant Physiol. 1982, 70:671-676.
44. Matheson N.K., Wheatley J.M. Starch changes in developing and senescing tobacco leaves. Aust. J. Biol. Sci. 1962, 15:445-458.
45. Matheson N.K., Wheatley J.M. Diurnal-nocturnal changes in starch of tobacco leaves. Aust. J. Biol. Sci. 1963, 16:70-76.
46. Vriet C., et al. A suite of Lotus japonicus starch mutants reveals both conserved and novel features of starch metabolism. Plant Physiol. 2010, 154:643-655.
47. Geiger D.R., et al. Photosynthetic carbon metabolism and translocation in wild-type and starch-deficient mutant Nicotiana sylvestris L. Plant Physiol. 1995, 107:507-514.
48. Harrison C.J., et al. Evidence that the rug3 locus of pea (Pisum sativum L.) encodes plastidial phosphoglucomutase confirms that the imported substrate for starch synthesis in pea amyloplasts is glucose-6-phosphate. Plant J. 1998, 13:753-762.
49. Vijn I., Smeekens S. Fructan: More than a reserve carbohydrate?. Plant Physiol. 1999, 120:351-359.