Endogenous Plant Rhythms (Annual Plant Reviews, Volume 21) by Anthony J. W. Hall, Harriet G. McWatters

By Anthony J. W. Hall, Harriet G. McWatters

Our wisdom of the circadian clock in vegetation has complex significantly lately and we've got a clearer view of the biochemical techniques making up its mechanism. fresh paintings presents perception into the crucial function performed via the circadian process within the legislation of many facets of metabolism. The a number of structures interested by photoreception were decided, resulting in an knowing of the way gentle entrains the inner organic clock to the ordinary cycle of day and evening, and the way this affects on key occasions within the plant lifecycle, equivalent to the photoperiodic rules of flowering.This booklet offers a modern evaluate of endogenous plant rhythms for researchers and pros within the plant sciences. it is going to additionally function a precious resource of reference for the broader circadian group.

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Sci. USA, 97, 9789–9794. R. A. (2003) FKF1 is essential for photoperiodic-specific light signaling in Arabidopsis. Nature, 426, 302–306. , Yamashino, T. & Mizuno, T. (2002) Characterization of the APRR9 pseudo-response regulator belonging to the APRR1/TOC1 quintet in Arabidopsis thaliana. , 44, 1237–1245. A. H. (2003) Arabidopsis PSEUDO-RESPONSE REGULATOR7 (PRR7) is a signaling intermediate in phytochrome-regulated seedling deetiolation and phasing of the circadian clock. Plant Cell, 15, 2654–2665.

B. (2003) DNA arrays: Applications and implications for circadian biology. J. Biol. Rhythms, 18, 96–105. A. B. (2004) A functional genomics strategy reveals Rora as a component of the mammalian circadian clock. Neuron, 43, 527–537. , Larson, M. & Wisman, E. (2001) Microarray analysis of diurnal and circadian-regulated genes in Arabidopsis. Plant Cell, 13, 113–123. A. & Coupland, G. (1998) The late elongated hypocotyl mutation of Arabidopsis disrupts circadian rhythms and the photoperiodic control of flowering.

2003b). A phase response curve to examine the response of expression of CAT3, CAB2 and TOC1 to cold pulses throughout the circadian cycle revealed that the phase of CAT3 expression is significantly more sensitive to temperature pulses than either CAB2 or TOC1 expression, suggesting that the oscillator driving CAT3 is different from the TOC1 oscillator. Dissection of these independent, potentially separate, oscillators will require identification of tissue- and temperature-specific promoters, which can be used in luciferase reporter constructs for forward genetic screens.

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