Abstract

BackgroundThe phenylpropanoid pathway is responsible for the synthesis of numerous compounds important for plant growth and responses to the environment. In the first committed step of phenylpropanoid biosynthesis, the enzyme phenylalanine ammonia-lyase (PAL) deaminates L-phenylalanine into trans-cinnamic acid that is then converted into p-coumaric acid by cinnamate-4-hydroxylase (C4H). Recent studies showed that the Kelch repeat F-box (KFB) protein family of ubiquitin ligases control phenylpropanoid biosynthesis by promoting the proteolysis of PAL. However, this ubiquitin ligase family, alternatively named Kiss Me Deadly (KMD), was also implicated in cytokinin signaling as it was shown to promote the degradation of type-B ARRs, including the key response activator ARR1. Considering that ubiquitin ligases typically have narrow target specificity, this dual targeting of structurally and functionally unrelated proteins appeared unusual.ResultsHere we show that the KFBs indeed target PAL but not ARR1. Moreover, we show that changes in early phenylpropanoid biosynthesis alter cytokinin sensitivity – as reported earlier - but that the previously documented cytokinin growth response changes are primarily the result of altered auxin signaling. We found that reduced PAL accumulation decreased, whereas the loss of C4H function increased the strength of the auxin response. The combined loss of function of both enzymes led to a decrease in auxin sensitivity, indicating that metabolic events upstream of C4H control auxin sensitivity. This auxin/phenylpropanoid interaction impacts both shoot and root development and revealed an auxin-dependent stimulatory effect of trans-cinnamic acid feeding on leaf expansion and thus biomass accumulation.ConclusionsCollectively, our results show that auxin-regulated plant growth is fine-tuned by early steps in phenylpropanoid biosynthesis and suggest that metabolites accumulating upstream of the C4H step impact the auxin response mechanism.

Highlights

  • The phenylpropanoid pathway is responsible for the synthesis of numerous compounds important for plant growth and responses to the environment

  • PP biosynthesis starts with L-phenylalanine that is converted into trans-cinnamic acid (t-CA) by phenylalanine ammonia lyase (PAL). t-CA can be converted to Kurepa et al BMC Plant Biology (2018) 18:278 cis-cinnamic acid (c-CA) by light and this photoisomer has been shown to inhibit auxin transport [10, 11]

  • Earlier studies revealed that KMD1/ KFB20 OE lines are dwarfed and that the extent of growth retardation is positively correlated with the expression level of the transgene [14, 15]

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Summary

Introduction

The phenylpropanoid pathway is responsible for the synthesis of numerous compounds important for plant growth and responses to the environment. In the first committed step of phenylpropanoid biosynthesis, the enzyme phenylalanine ammonia-lyase (PAL) deaminates L-phenylalanine into trans-cinnamic acid that is converted into p-coumaric acid by cinnamate-4-hydroxylase (C4H). Recent studies showed that the Kelch repeat Fbox (KFB) protein family of ubiquitin ligases control phenylpropanoid biosynthesis by promoting the proteolysis of PAL. This ubiquitin ligase family, alternatively named Kiss Me Deadly (KMD), was implicated in cytokinin signaling as it was shown to promote the degradation of type-B ARRs, including the key response activator ARR1. PP biosynthesis starts with L-phenylalanine that is converted into trans-cinnamic acid (t-CA) by phenylalanine ammonia lyase (PAL). Arabidopsis mutants that are defective in specific steps of flavonoid biosynthesis show auxin-related developmental phenotypes [12]

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