Abstract

BackgroundPectin methylesterase (PME, EC 3.1.1.11) is a hydrolytic enzyme that utilizes pectin as substrates, and plays a significant role in regulating pectin reconstruction thereby regulating plant growth. Pectin is one of the important components of the plant cell wall, which forms the main structural material of cotton fiber. In this research, cotton genome information was used to identify PMEs.ResultsWe identified 80 (GaPME01-GaPME80) PME genes from diploid G. arboreum (A genome), 78 (GrPME01-GrPME78) PME genes from G. raimondii (D genome), and 135 (GhPME001-GhPME135) PME genes from tetraploid cotton G. hirsutum (AD genome). We further analyzed their gene structure, conserved domain, gene expression, and systematic evolution to lay the foundation for deeper research on the function of PMEs. Phylogenetic data indicated that members from the same species demonstrated relatively high sequence identities and genetic similarities. Analysis of gene structures showed that most of the PMEs genes had 2–3 exons, with a few having a variable number of exons from 4 to 6. There are nearly no differences in the gene structure of PMEs among the three (two diploid and one tetraploid) cotton species. Selective pressure analysis showed that the Ka/Ks value for each of the three cotton species PME families was less than one.ConclusionConserved domain analysis showed that PMEs members had a relatively conserved C-terminal pectinesterase domain (PME) while the N-terminus was less conserved. Moreover, some of the family members contained a pectin methylesterase inhibitor (PMEI) domain. The Ka/Ks ratios suggested that the duplicated PMEs underwent purifying selection after the duplication events. This study provided an important basis for further research on the functions of cotton PMEs. Results from qRT-PCR indicated that the expression level of different PMEs at various fiber developmental stages was different. Moreover, some of the PMEs showed fiber predominant expression in secondary wall thickening indicating tissue-specific expression patterns.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-3365-z) contains supplementary material, which is available to authorized users.

Highlights

  • Pectin methylesterase (PME, EC 3.1.1.11) is a hydrolytic enzyme that utilizes pectin as substrates, and plays a significant role in regulating pectin reconstruction thereby regulating plant growth

  • Identification of cotton PMEs From the three cotton genomes (AD, A, and D), we identified 135 full-length putative G. hirsutum PMEs (GhPME001-135), 80 full-length putative G. arboretum PMEs (GaPME01-GaPME80), and 78 full-length putative G. raimondii PMEs (GrPME01-GrPME78)

  • The length of the exons in PMEs ranged from 1045 bp to 13398 bp in G. arboreum, 1045 bp to 6730 bp in G. raimondii, and 964 bp to 4695 bp in G. hirsutum (Additional file 1: Table S1)

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Summary

Introduction

Pectin methylesterase (PME, EC 3.1.1.11) is a hydrolytic enzyme that utilizes pectin as substrates, and plays a significant role in regulating pectin reconstruction thereby regulating plant growth. Pectin is one of the important components of the plant cell wall, which forms the main structural material of cotton fiber. Cotton genome information was used to identify PMEs. Cotton (Gossypium spp.) is one of the most important natural fiber crops around the world. The improvement of cotton fiber quality is becoming increasingly important and is a main focal point of cotton research [1, 2]. Pectin is an important component of cotton fiber and pectin metabolism may influence fiber quality. Previous studies showed that PMEs play an important role in the process of fiber development by influencing the chemical properties of pectin [1]. Process of cotton fiber cell developing was purposely divided into four relative independent but overlapping stages: fiber initiation, elongation, secondary wall biosynthesis and maturation [3]. The increasing thickness of the fiber secondary wall gradually increases the strength of fibers

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