Phosphate Availability Alters Architecture and Causes Changes in Hormone Sensitivity in the Arabidopsis Root System1

By J. López‐Bucio, E. Hernández-Abreu, L. Sánchez-Calderón, M. Nieto-Jacobo, J. Simpson, L. Herrera-Estrella. Plant Physiology, 2002

745 citations recorded by the source corpus.

Subfields: Plant Science

View Paper: https://www.semanticscholar.org/paper/096bc4acf8f2ec9b1135775438c92dfd0d7d7cf3

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. H. Lambers
3. P. White
4. M. Blair
5. T. Chiou
6. Shu-I. Lin
7. Steve Beebe
8. K. Brown

Citations in the corpus

• Detection of quantitative trait loci for phosphorus deficiency tolerance at soybean seedling stage (2009, neutral): “QTL mapping has been well conducted with P efficiency in Arabidopsis (López-Bucio et al. 2002; Ma et al. 2003; Wu et al. 2003), rice (Oryza sativa L.) (Ni et al. 1998; Wissuwa et al. 1998; Shimizu et al. 2004), maize (Zea mays L.) (Reiter et al. 1991; Zhu et al. 2005, 2006), wheat (Triticum…”
• Intrinsic and environmental response pathways that regulate root system architecture. (2005, background): “Similarly, Lopez-Bucio et al. (2002) observed that Arabidopsis plants grown under low phosphate have an increased lateral root number and density.”
• Manganese accumulation in leaves of Hakea prostrata (proteaceae) and the significance of cluster roots for micronutrient uptake as dependent on phosphorus supply (2005, background): “The latter mechanism has been suggested to account for lateral-root initiation by Arabidopsis thaliana growing under conditions of low P availability (López-Bucio et al. 2002).”
• MicroRNA399 is a long-distance signal for the regulation of plant phosphate homeostasis (2008, background): “ing the root/shoot ratio (Lynch, 1995), alterations in root architecture (López-Bucio et al., 2002; Williamson et al., 2001), production of lateral roots into Pi-rich patches in the”
• The role of nutrient availability in regulating root architecture. (2003, background): “The auxin-transport inhibitors 2,3,5-triiodobenzoic acid (TIBA) and N-(1-napthyl)phtalamic acid (NPA) were found to inhibit the formation of proteoid or lateral roots in Lupin and Arabidopsis, respectively [24 ,34].”
• Combining a modelling with a genetic approach in establishing associations between genetic and physiological effects in relation to phosphorus uptake (2005, background): “Under conditions of P deficiency plants typically undergo several changes in root morphology that increase the root to shoot ratio (Lopez-Bucio et al., 2002) and root hair density and length (Ma et al., 2001) while also affecting the balance between root elongation, lateral root growth and root…”
• ROOT STRATEGIES FOR PHOSPHORUS ACQUISITION (2008, background): “In Arabidopsis seedlings deprived of added P, lateral root number was also reduced, but in this case the remaining lateral roots elongated at the expense of the primary root (Williamson et al. 2001; Lopez-Bucio et al. 2002; Al-Ghazi et al. 2003).”
• Nutrient Sensing and Signalling in Plants: Potassium and Phosphorus (2005, background): “Plants lacking P are also more sensitive to an auxin‐induced increase in lateral root number and density (López‐Bucio et al., 2002).”
• Root Development and Nutrient Uptake (2006, background): “On the other hand, López-Bucio et al. (2002) reported that phosphate-starved Arabidopsis plants were more sensitive to auxin induction of lateral roots than control plants.”