Abstract

A 1670 bp 5′-flanking region of the polyphenol oxidase (PPO) gene was isolated from red Swiss chard, a betalain-producing plant. This region, named promoter BvcPPOP, and its 5′-truncated versions were fused with the GUS gene and introduced into Arabidopsis, an anthocyanins-producing plant. GUS histochemical staining and quantitative analysis of transgenic plants at the vegetative and reproductive stages showed that BvcPPOP could direct GUS gene expression in vegetative organs with root- and petiole-preference, but not in reproductive organs including inflorescences shoot, inflorescences leaf, flower, pod and seed. This promoter was regulated by developmental stages in its driving strength, but not in expression pattern. It was also regulated by the abiotic stressors tested, positively by salicylic acid (SA) and methyl jasmonate (MeJA) but negatively by abscisic acid (ABA), gibberellin (GA), NaCl and OH−. Its four 5′-truncated versions varied in the driving strength, but not obviously in expression pattern, and even the shortest version (−225 to +22) retained the root- and petiole- preference. This promoter is, to our knowledge, the first PPO promoter cloned and functionally elucidated from the betalain-producing plant, and thus provides not only a useful tool for expressing gene(s) of agricultural interest in vegetative organs, but also a clue to clarify the function of metabolism-specific PPO in betalain biosynthesis.

Highlights

  • IntroductionPolyphenol oxidases (PPOs) are type-3 copper enzymes that can catalyze the o-hydroxylation of monophenols (monophenolase activity, EC 1.14.18.1) and oxidation of o-diphenols to o-quinones (diphenolase activity, catechol oxidase activity, EC 1.10.3.1)

  • Polyphenol oxidases (PPOs) are type-3 copper enzymes that can catalyze the o-hydroxylation of monophenols and oxidation of o-diphenols to o-quinones

  • PPOs can be classified into two groups based on their physiological roles: Group 1: PPOs engaged in adaptation and defense against biotic and abiotic stresses; Group 2: PPOs involved in some specific secondary metabolisms [1,2]

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Summary

Introduction

Polyphenol oxidases (PPOs) are type-3 copper enzymes that can catalyze the o-hydroxylation of monophenols (monophenolase activity, EC 1.14.18.1) and oxidation of o-diphenols to o-quinones (diphenolase activity, catechol oxidase activity, EC 1.10.3.1). They are widely distributed in plants, animals and microbes. PPOs can be classified into two groups based on their physiological roles: Group 1: PPOs engaged in adaptation and defense against biotic and abiotic stresses; Group 2: PPOs involved in some specific secondary metabolisms [1,2]. The 5t1r-adneslgeetnedic vaenrthsioocnysandiind-parsodwuecliln, gbuptlaantt,dAifrfaebreidnotplesivse, lws.itThhaerionofto- ramndatpioetniorleep-porretfeedrenhteirael pmaattyerhne. lp to undeTrshtean5′d-dwelheteetdhevrertshioenPsPdOidiassewngelal,gbeudt iant bdeiftfaelraeinnt lbeivoeslys.nTthheesiinsf,oarmt laetaiostnirnepreodrteSdwhiesrsecmhaarydh, ealnpd the promtootuerndaenrdstaitnsd5w1-dheetlheeter dthveePrPsOionissednigsacgloedseidn bheetraelaminabyiopsyronvthideseisu, saet fluealsttoionlrsefdoSrwcrisospchimarpdr, oavndement via bitohteecphrnoomlotgeyr raonudte.its 5′-deleted versions disclosed here may provide useful tools for crop improvement via biotechnology route

Results
Discussion
Plant Materials and Growth Conditions
Isolation of the Promoter and Its Deletion Analysis
Analysis of GUS Expression
Abiotic Stress Treatment
Conclusions
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