Abstract

Pectin is a critical component of the plant cell wall, supporting wall biomechanics and contributing to cell wall signaling in response to stress. The plant cell carefully regulates pectin methylesterification with endogenous pectin methylesterases (PMEs) and their inhibitors (PMEIs) to promote growth and protect against pathogens. We expressed Aspergillus nidulans pectin methylesterase (AnPME) in Arabidopsis thaliana plants to determine the impacts of methylesterification status on pectin function. Plants expressing AnPME had a roughly 50% reduction in methylester content compared with control plants. AnPME plants displayed a severe dwarf phenotype, including small, bushy rosettes and shorter roots. This phenotype was caused by a reduction in cell elongation. Cell wall composition was altered in AnPME plants, with significantly more arabinose and significantly less galacturonic acid, suggesting that plants actively monitor and compensate for altered pectin content. Cell walls of AnPME plants were more readily degraded by polygalacturonase (PG) alone but were less susceptible to treatment with a mixture of PG and PME. AnPME plants were insensitive to osmotic stress, and their susceptibility to Botrytis cinerea was comparable to wild type plants despite their compromised cell walls. This is likely due to upregulated expression of defense response genes observed in AnPME plants. These results demonstrate the importance of pectin in both normal growth and development, and in response to biotic and abiotic stresses.

Highlights

  • The plant cell wall is an important, complex component of all plant cells

  • This study explores the role of pectin methylesterification in cell wall integrity (CWI) and the impact of cell wall de-esterification on plant growth and stress response

  • Three independent homozygous transgenic events were selected for this study based on their varying degree of phenotype shown (AnPME 1-1, 2-1, and 3-2)

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Summary

Introduction

The plant cell wall is an important, complex component of all plant cells. The polysaccharides of the primary cell wall make up the bulk of its dry weight and are divided into three categories: cellulose, hemicelluloses, and pectins [2]. Pectins are acidic heteropolymers of three distinct types containing galacturonic acid (GalA). Homogalacturonan (HG) is composed of unbranched α-1,4-linked GalA residues that are gradually demethylesterified as the plant ages [4,5]. Rhamnogalacturonan I (RG-I) is composed of alternating α-1,4-GalA and α-1,2-Rhamnose (Rha) residues with sidechains of varying composition [6], and rhamnogalacturonan II (RG-II) is composed of an α-1,4-linked GalA backbone with complex sidechains [6,7,8]. Pectins exist as continuous heteropolymers in muro with long stretches of HG interspersed between shorter stretches of RG-I and RG-II [9]

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