Control of plant development and gene expression by sugar signaling.

By S. Gibson. Current opinion in plant biology, 2005

680 citations recorded by the source corpus.

Subfields: Plant Science

View Paper: https://www.semanticscholar.org/paper/851af5f17ace23ff68fa727e78e4a0b75384acde

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Plant Science

1. J. Lynch
2. R. Finkelstein
3. L. Bentsink
4. F. Rolland
5. Jen Sheen
6. M. Koornneef
7. R. Jaramillo
8. M. Yusuf

Citations in the corpus

• The Flowering Process of Vitis vinifera: A Review (2009, background): “The reader is encouraged to consult the suggested reviews for a background to this expansive topic (Gibson 2005, Irish 2008, Kramer and Hall 2005, Krizek and Fletcher 2005, Krizek 2006, Sablowski 2007).”
• Role of sugars under abiotic stress. (2016, background): “In dark grown Arabidopsis seedlings, sucrose, glucose and fructose were stimulated the formation of adventitious roots (Gibson, 2005).”
• Sugars and Circadian Regulation Make Major Contributions to the Global Regulation of Diurnal Gene Expression in Arabidopsis[W][OA] (2005, background): “There has been considerable interest in the genetic and molecular analysis of responses to high sugar (Gibson, 2005; Rolland and Sheen, 2005).”
• Anthocyanin Function in Vegetative Organs (2008, background): “Soluble sugars, especially sucrose, glucose, and fructose, are now known to play central roles in the control of plant development, stress responses, and gene expression ( Gibson 2005 ).”
• Abscisic Acid Synthesis and Response (2013, background): “, Gibson, S. (2000). The Arabidopsis sugarinsensitive mutants sis4 and sis5 are defective in abscisic acid synthesis and response.”
• Sugar sensing and signaling in plants: conserved and novel mechanisms. (2006, background): “The glucoseinsensitive sis4/gin1 mutants are allelic to aba2, which is deficient in a short-chain dehydrogenase/reductase (SDR1) required for ABA synthesis (21, 43, 76).”
• Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “In addition to inhibition of seed germination, glucose can also arrest the post-germination growth (Jang and Sheen, 1997; Gibson, 2005).”
• Sucrose-Specific Induction of Anthocyanin Biosynthesis in Arabidopsis Requires the MYB75/PAP1 Gene1 (2005, background): “Elevated sugar levels induce developmental arrest of postgerminated seedlings in Arabidopsis (Arabidopsis thaliana), and this has been one of the principles used to identify mutants in sugar signaling (Smeekens, 2000; Rolland et al., 2002; Rook and Bevan, 2003; Gibson, 2005).”
• Architectural Tradeoffs between Adventitious and Basal Roots for Phosphorus Acquisition (2005, background): “…benefit of adventitious roots for phosphorus acquisition and efficiency with reduced C allocation to roots provides an explanation as to why reduced C availability in Arabidopsis and maize leads to decreased or delayed adventitious rooting (Gibson, 2005; Pellerin, 1991; Takahashi et al., 2003).”
• Drought-induced Accumulation of Soluble Sugars and Proline in Two Maize Varieties (2008, neutral): “Recently it has been claimed that even sugar flux may be a signal for metabolic regulation [32].”
• Exogenous nitric oxide protects against salt-induced oxidative stress in the leaves from two genotypes of tomato (Lycopersicom esculentum Mill.) (2011, background): “Recently it has been claimed that even sugar flux may be a signal for metabolic regulation (Gibson 2005).”