Abstract

Strigolactones (SLs) are essential host recognition signals for both root-parasitic plants and arbuscular mycorrhizal (AM) fungi in the rhizosphere, and in planta SLs or their metabolites function as a novel class of plant hormones that regulate various aspects of plant growth through crosstalk with other hormones. Although nutrient availability is one of the important factors influencing SL production and exudation, and phosphate (Pi) deficiency significantly promotes SL production and exudation in host plants of AM fungi, how nutrient availability modulates SL production and exudation remains elusive. Cytokinin (CK), a canonical plant hormone, has extensively been studied as a shoot branching promoter and its biosynthesis is also influenced by mineral nutrients, especially nitrate, indicating that CK might be another key factor that affect SL production and exudation. In the present study, we show that CKs (t-zeatin, benzyladenine, kinetin, and CPPU) applied to hydroponic culture media significantly suppressed the SL levels in both the root exudates and the root tissues of rice plants grown under Pi deficiency. In a split-root system, CK suppressed SL production locally, while Pi affected SL production systemically, suggesting that Pi and CK act on SL production independently in rice plants.

Highlights

  • Strigolactones (SLs) exuded from plant roots are essential host recognition signals for both rootparasitic plants (Cook et al, 1966) and arbuscular mycorrhizal (AM) fungi (Akiyama et al, 2005) in the rhizosphere

  • CPPU [N-(2-chloro-4-pyridyl)-N’-phenylurea], a phenylureatype CK which is structurally distinct from adenine-type CKs, suppressed 4DO levels, suggesting that this inhibitory effect on 4DO production is attributable to CK activity

  • We demonstrated that CK, a canonical plant hormone known as a shoot-branching promoter, is a negative regulator for SL production and exudation in rice plants

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Summary

Introduction

Strigolactones (SLs) exuded from plant roots are essential host recognition signals for both rootparasitic plants (Cook et al, 1966) and arbuscular mycorrhizal (AM) fungi (Akiyama et al, 2005) in the rhizosphere. Root-parasitic plants deprive water and nutrients from their host plants, causing severe damages to the host plants. Most of the root-parasitic plants are generally regarded as agricultural pests. AM fungi stay in the cortical tissues of host roots and supply mineral nutrients, mainly phosphate (Pi), to the host plants. The interactions between rootparasitic plants and symbiotic AM fungi with their host plants have been reported to be influenced by nutrient availability in the soil; fertilizations mitigate the damages of root-parasitic weeds growing on nutrient-poor soils but inhibit AM colonization. Since SL production and exudation are regulated by plant nutrients including Pi and nitrogen (N) (Yoneyama et al, 2007a,b), nutrient

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