Malate-dependent Fe accumulation is a critical checkpoint in the root developmental response to low phosphate.

Abstract

Low phosphate (Pi) availability constrains plant development and seed production in both natural and agricultural ecosystems. When Pi is scarce, modifications of root system architecture (RSA) enhance the soil exploration ability of the plant and lead to an increase in Pi uptake. In <i>Arabidopsis</i>, an iron-dependent mechanism reprograms primary root growth in response to low Pi availability. This program is activated upon contact of the root tip with low-Pi media and induces premature cell differentiation and the arrest of mitotic activity in the root apical meristem, resulting in a short-root phenotype. However, the mechanisms that regulate the primary root response to Pi-limiting conditions remain largely unknown. Here we report on the isolation and characterization of two low-Pi insensitive mutants (<i>lpi5</i> and <i>lpi6</i>), which have a long-root phenotype when grown in low-Pi media. Cellular, genomic, and transcriptomic analysis of low-Pi insensitive mutants revealed that the genes previously shown to underlie <i>Arabidopsis</i> Al tolerance via root malate exudation, known as SENSITIVE TO PROTON RHIZOTOXICITY (<i>STOP1</i>) and ALUMINUM ACTIVATED MALATE TRANSPORTER 1 (<i>ALMT1</i>), represent a critical checkpoint in the root developmental response to Pi starvation in <i>Arabidopsis thaliana</i> Our results also show that exogenous malate can rescue the long-root phenotype of <i>lpi5</i> and <i>lpi6</i> Malate exudation is required for the accumulation of Fe in the apoplast of meristematic cells, triggering the differentiation of meristematic cells in response to Pi deprivation.