Abstract

BackgroundMultidrug and toxic compound extrusion (MATE) transporter proteins are present in all organisms. Although the functions of some MATE gene family members have been studied in plants, few studies have investigated the gene expansion patterns, functional divergence, or the effects of positive selection.ResultsForty-five MATE genes from rice and 56 from Arabidopsis were identified and grouped into four subfamilies. MATE family genes have similar exon-intron structures in rice and Arabidopsis; MATE gene structures are conserved in each subfamily but differ among subfamilies. In both species, the MATE gene family has expanded mainly through tandem and segmental duplications. A transcriptome atlas showed considerable differences in expression among the genes, in terms of transcript abundance and expression patterns under normal growth conditions, indicating wide functional divergence in this family. In both rice and Arabidopsis, the MATE genes showed consistent functional divergence trends, with highly significant Type-I divergence in each subfamily, while Type-II divergence mainly occurred in subfamily III. The Type-II coefficients between rice subfamilies I/III, II/III, and IV/III were all significantly greater than zero, while only the Type-II coefficient between Arabidopsis IV/III subfamilies was significantly greater than zero.A site-specific model analysis indicated that MATE genes have relatively conserved evolutionary trends. A branch-site model suggested that the extent of positive selection on each subfamily of rice and Arabidopsis was different: subfamily II of Arabidopsis showed higher positive selection than other subfamilies, whereas in rice, positive selection was highest in subfamily III. In addition, the analyses identified 18 rice sites and 7 Arabidopsis sites that were responsible for positive selection and for Type-I and Type-II functional divergence; there were no common sites between rice and Arabidopsis. Five coevolving amino acid sites were identified in rice and three in Arabidopsis; these sites might have important roles in maintaining local structural stability and protein functional domains.ConclusionsWe demonstrate that the MATE gene family expanded through tandem and segmental duplication in both rice and Arabidopsis. Overall, the results of our analyses contribute to improved understanding of the molecular evolution and functions of the MATE gene family in plants.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-016-0895-0) contains supplementary material, which is available to authorized users.

Highlights

  • Multidrug and toxic compound extrusion (MATE) transporter proteins are present in all organisms

  • A BLASTP search of the Phytozome database identified 45 MATE genes in Oryza sativa and 56 in Arabidopsis thaliana. Both PFAM and Simple Modular Architecture Research Tool (SMART) databases confirmed the presence of the conserved domain in the MATE gene family

  • The 56 Arabidopsis genes encoded proteins with amino acid sequence lengths of 469 to 575 amino acids, molecular weights from 50.8 to 63.5 kD, and pI values ranging from 4.66 to 8.67. These results implied that the amino acid sequence length and physicochemical properties of rice and Arabidopsis MATE proteins might have changed to meet different functions

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Summary

Introduction

Multidrug and toxic compound extrusion (MATE) transporter proteins are present in all organisms. Plants are routinely exposed to exogenous toxins secreted by other organisms or pathogenic microbes and to endogenous toxins produced by metabolic processes. Disposal and detoxification of toxic compounds of both exogenous and endogenous origin are important processes for survival and development. Integral membrane proteins named ‘multidrug resistance transporter’ are important drug resistance pumps as they can extrude structurally and chemically distinct drugs from cells, giving rise to multidrug resistance [10, 11]. Multidrug transporters are classified into five main groups [8, 12]: ATP-binding cassette (ABC), major facilitator superfamily (MFS), resistance-nodulation-division (RND), small multidrug resistance (SMR) transporters, and multidrug and toxic compound extrusion (MATE) families. The primary ABC transporters use the energy of ATP hydrolysis to transport drugs, whereas the other families are secondary transporters that use H+ or Na+ electrochemical gradients to drive substrate export

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