Cloning of the Arabidopsis clock gene TOC1, an autoregulatory response regulator homolog.
By C. Strayer, T. Oyama, T. F. Schultz, Ramanujam Raman, D. Somers, P. Más, Satchidananda Panda, J. Kreps, Steve A. Kay. Science, 2000
864 citations recorded by the source corpus.
Subfields: Endocrine and Autonomic Systems, Plant Science
View Paper: https://www.semanticscholar.org/paper/0f63b365c4418268e06a6061d149a779507ff44a
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In Endocrine and Autonomic Systems
In Plant Science
Citations in the corpus
- FKF1 is essential for photoperiodic-specific light signalling in Arabidopsis (2003, background): “The phase and the amplitude of two circadian reporters (gene fusions of the luciferase ( luc ) promoter and CHLOROPHYLL A/B BINDING PROTEIN 2 ( CAB2 ) or COLD CIRCADIAN RNA BINDING PROTEIN 2 ; CCR2”
- Molecular mechanisms of polyploidy and hybrid vigor (2010, background): “CCA1 and LHY negatively regulate TOC1 and GI expression, whereas TOC1 binds to the CCA1 promoter and interacts with CHE, positively regulating CCA1 and LHY expression [89-91,93].”
- The Arabidopsis Cold-Responsive Transcriptome and Its Regulation by ICE1w⃞ (2005, background): “APRR1 is also called TIMING OF CAB EXPRESSION1 and is an essential component of the central oscillator for circadian rhythms in Arabidopsis (Strayer et al., 2000; Mizuno, 2004).”
- What makes the Arabidopsis clock tick on time? A review on entrainment (2005, background): “It is interesting that the CCT domain of TOC1 has a very high PEST score (+16.67; http://www.at.embnet.org/embnet/ tools/bio/PESTfind/) and that the mutation in toc1-1 lies very close to the beginning of this putative PEST sequence (Strayer et al. 2000).”
- A Pseudo-Response Regulator is misexpressed in the photoperiod insensitive Ppd-D1a mutant of wheat (Triticum aestivum L.) (2007, background): “Five PRR genes are present in Arabidopsis and rice (Matsushika et al. 2000; Murakami et al. 2003, respectively) and they are best characterized in the former where PRR1 (TOC1) is part of the central oscillator of the circadian clock (Strayer et al. 2000).”
- Multiple Pathways in the Decision to Flower: Enabling, Promoting, and Resetting (2004, background): “Only under long days would high CO mRNA levels coincide with light, leading to an increase in FT expression (Suárez-López et al., 2001).”
- Control of flowering time: interacting pathways as a basis for diversity. (2002, background): “The toc1 mutant flowered early in short days (Kreps and Simon, 1997; Somers et al., 1998b), and this phenotype could be rescued by growing the plants in daily cycles of 21 h rather than 24 h, a reduction of 3 h corresponding to the shorter period length observed in toc1 (Strayer et al., 2000).”
- Plant Circadian Rhythms (2006, background): “TOC1 contains a CCT (for CONSTANS, CONSTANSLIKE, TOC1) domain thought to be involved in transcription (Strayer et al., 2000) but has not been shown to bind to either CCA1 or LHY promoters.”
- Light-regulated transcriptional networks in higher plants (2007, background): “, and the evening-expressing TIMING OF CAB EXPRESSION 1 ( TOC1 ; also known as PRR1”
- Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice (2008, methodology): “We scanned the predicted proteins and found that one of the genes encodes a protein with homology to the CCT domain (see below), present in the CO , CO -like ( COL ) and TOC1 gene products, which have been extensively analyzed and shown to regulate flowering time in Arabidopsis”
- The 14-3-3 Proteins μ and υ Influence Transition to Flowering and Early Phytochrome Response1[C][OA] (2007, background): “CO has a CO, CO-like, and CCT (timing of CAB1) domain (Putterill et al., 1995), a conserved C-terminal protein-protein interaction domain shared with a suite of other proteins including TOC1 and CO-LIKE proteins (Strayer et al., 2000; Robson et al., 2001).”