Anatomy of a Motherboard Article by Marty Sems Lori Garris

By Marty Sems Lori Garris

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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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