Abstract

Expression of two Arabidopsis (Arabidopsis thaliana) apyrase (nucleoside triphosphate-diphosphohydrolase) genes with high similarity, APY1 and APY2, was analyzed during seedling development and under different light treatments using beta-glucuronidase fusion constructs with the promoters of both genes. As evaluated by beta-glucuronidase staining and independently confirmed by other methods, the highest expression of both apyrases was in rapidly growing tissues and/or tissues that accumulate high auxin levels. Red-light treatment of etiolated seedlings suppressed the protein and message level of both apyrases at least as rapidly as it inhibited hypocotyl growth. Adult apy1 and apy2 single mutants had near-normal growth, but apy1apy2 double-knockout plants were dwarf, due primarily to reduced cell elongation. Pollen tubes and etiolated hypocotyls overexpressing an apyrase had faster growth rates than wild-type plants. Growing pollen tubes released ATP into the growth medium and suppression of apyrase activity by antiapyrase antibodies or by inhibitors simultaneously increased medium ATP levels and inhibited pollen tube growth. These results imply that APY1 and APY2, like their homologs in animals, act to reduce the concentration of extracellular nucleotides, and that this function is important for the regulation of growth in Arabidopsis.

Highlights

  • Expression of two Arabidopsis (Arabidopsis thaliana) apyrase genes with high similarity, APY1 and APY2, was analyzed during seedling development and under different light treatments using b-glucuronidase fusion constructs with the promoters of both genes

  • These results reveal that expression of APY1 and APY2 is closely correlated with growth and we discuss ways their enzymatic function could participate in growth control

  • We report three lines of evidence that APY1 and APY2 play an important role in the control of plant cell growth: Transcript abundance for APY1 and APY2 is highest in tissues and cell types that are growing rapidly, constitutive expression of one of these genes results in enhanced growth of hypocotyls and pollen tubes, and suppression of both genes in Arabidopsis or chemical suppression of apyrase enzyme activity results in impaired growth

Read more

Summary

Introduction

Expression of two Arabidopsis (Arabidopsis thaliana) apyrase (nucleoside triphosphate-diphosphohydrolase) genes with high similarity, APY1 and APY2, was analyzed during seedling development and under different light treatments using b-glucuronidase fusion constructs with the promoters of both genes. Growing pollen tubes released ATP into the growth medium and suppression of apyrase activity by antiapyrase antibodies or by inhibitors simultaneously increased medium ATP levels and inhibited pollen tube growth. These results imply that APY1 and APY2, like their homologs in animals, act to reduce the concentration of extracellular nucleotides, and that this function is important for the regulation of growth in Arabidopsis. The majority of characterized apyrases are ectoapyrases (i.e. enzymes that are anchored in the plasma membrane with their active site pointing out into the Arabidopsis (Arabidopsis thaliana) has seven apyrases, two of which, APY1 and APY2, are most similar to the pea (Pisum sativum) ectoapyrase NTP9 (Steinebrunner et al, 2000). These results reveal that expression of APY1 and APY2 is closely correlated with growth and we discuss ways their enzymatic function could participate in growth control

Methods
Results
Conclusion
Full Text
Paper version not known

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

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.