Abstract

Recent evidence indicates that extracellular nucleotides regulate plant growth. Exogenous ATP has been shown to block auxin transport and gravitropic growth in primary roots of Arabidopsis (Arabidopsis thaliana). Cells limit the concentration of extracellular ATP in part through the activity of ectoapyrases (ectonucleoside triphosphate diphosphohydrolases), and two nearly identical Arabidopsis apyrases, APY1 and APY2, appear to share this function. These findings, plus the fact that suppression of APY1 and APY2 blocks growth in Arabidopsis, suggested that the expression of these apyrases could influence auxin transport. This report tests that hypothesis. The polar movement of [(3)H]indole-3-acetic acid in both hypocotyl sections and primary roots of Arabidopsis seedlings was measured. In both tissues, polar auxin transport was significantly reduced in apy2 null mutants when they were induced by estradiol to suppress the expression of APY1 by RNA interference. In the hypocotyl assays, the basal halves of APY-suppressed hypocotyls contained considerably lower free indole-3-acetic acid levels when compared with wild-type plants, and disrupted auxin transport in the APY-suppressed roots was reflected by their significant morphological abnormalities. When a green fluorescent protein fluorescence signal encoded by a DR5:green fluorescent protein construct was measured in primary roots whose apyrase expression was suppressed either genetically or chemically, the roots showed no signal asymmetry following gravistimulation, and both their growth and gravitropic curvature were inhibited. Chemicals that suppress apyrase activity also inhibit gravitropic curvature and, to a lesser extent, growth. Taken together, these results indicate that a critical step connecting apyrase suppression to growth suppression is the inhibition of polar auxin transport.

Highlights

  • Recent evidence indicates that extracellular nucleotides regulate plant growth

  • The results indicate that suppression of APY1/APY2 expression in an inducible RNA interference (RNAi) line, R2-4A (Wu et al, 2007), results in a significant inhibition of polar auxin transport in Arabidopsis hypocotyls and roots, with a concomitant altered distribution of endogenous auxin

  • To determine if APY1 and APY2 play a role in auxin transport, we assayed polar auxin transport in hypocotyls of loss- and gain-of-function apyrase mutants, including the RNAi line R2-4A, in which the expression of APY1 in the apy2 null background can be suppressed by estradiol treatment

Read more

Summary

Introduction

Recent evidence indicates that extracellular nucleotides regulate plant growth. Exogenous ATP has been shown to block auxin transport and gravitropic growth in primary roots of Arabidopsis (Arabidopsis thaliana). Cells limit the concentration of extracellular ATP in part through the activity of ectoapyrases (ectonucleoside triphosphate diphosphohydrolases), and two nearly identical Arabidopsis apyrases, APY1 and APY2, appear to share this function These findings, plus the fact that suppression of APY1 and APY2 blocks growth in Arabidopsis, suggested that the expression of these apyrases could influence auxin transport. These results indicate that a critical step connecting apyrase suppression to growth suppression is the inhibition of polar auxin transport In both animals and plants, cells release nucleotides into their extracellular matrix, where they function as signaling agents, inducing rapid increases in the concentration of cytosolic calcium that are transduced into downstream changes in cell physiology (Kim et al., 2006; Burnstock, 2007; Roux and Steinebrunner, 2007; Tanaka et al, 2010a, 2010b; Demidchik et al, 2011). There is strong evidence that APY1 and APY2 are localized in the Golgi and may function there to regulate protein glycosylation and/or affect polysaccharide synthesis (Chiu et al, 2012; Schiller et al, 2012)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call