Abstract

Multidrug and toxic compound extrusion (MATE) transporters comprise a multigene family that mediates multiple functions in plants through the efflux of diverse substrates including organic molecules, specialized metabolites, hormones, and xenobiotics. MATE classification based on genome-wide studies remains ambiguous, likely due to a lack of large-scale phylogenomic studies and/or reference sequence datasets. To resolve this, we established a phylogeny of the plant MATE gene family using a comprehensive kingdom-wide phylogenomic analysis of 74 diverse plant species. We identified more than 4,000 MATEs, which were classified into 14 subgroups based on a systematic bioinformatics pipeline using USEARCH, blast+ and synteny network tools. Our classification was performed using a four-step process, whereby MATEs sharing ≥ 60% protein sequence identity with a ≤ 1E-05 threshold at different sequence lengths (either full-length, ≥ 60% length, or ≥ 150 amino acids) or retaining in the similar synteny blocks were assigned to the same subgroup. In this way, we assigned subgroups to 95.8% of the identified MATEs, which we substantiated using synteny network clustering analysis. The subgroups were clustered under four major phylogenetic groups and named according to their clockwise appearance within each group. We then generated a reference sequence dataset, the usefulness of which was demonstrated in the classification of MATEs in additional species not included in the original analysis. Approximately 74% of the plant MATEs exhibited synteny relationships with angiosperm-wide or lineage-, order/family-, and species-specific conservation. Most subgroups evolved independently, and their distinct evolutionary trends were likely associated with the development of functional novelties or the maintenance of conserved functions. Together with the systematic classification and synteny network profiling analyses, we identified all the major evolutionary events experienced by the MATE gene family in plants. We believe that our findings and the reference dataset provide a valuable resource to guide future functional studies aiming to explore the key roles of MATEs in different aspects of plant physiology. Our classification framework can also be readily extendable to other (super) families.

Highlights

  • We identify a total of 4,211 Multidrug and toxic compound extrusion (MATE) using a hidden Markov model (HMM) profile-based search and classify these into 14 subgroups based on sequence homology and synteny relationships using a four-step process

  • Phylogenomic profiling was performed based on the HMM profile of the MATE gene family (PF01554.19) to explore the complete repertoire of MATEs in the plant kingdom (Supplementary Table 1)

  • We presumed that the existence of non-specific or multiple MatE domains in a single hmmsearch hit resulted from an annotation and/or genome assembly pipeline error

Read more

Summary

Introduction

A large class of proteins embedded in cell membranes facilitates both the inward and outward passage of cellular solutes based on diffusion or electrochemical gradients These proteins serve to maintain cell integrity and can be broadly categorized into channels, pumps, transporters, and other carriers (Tang et al, 2020). Multidrug and toxic compound extrusion (MATE) proteins form one of the major multidrug transporter families that intercept the secondary transport of heterogenic cytotoxic compounds using either proton (H+) or sodium ion (Na+) gradients. These proteins are ubiquitous across all three domains of life and are presumed to have evolved from a common ancestral gene via duplication (Omote et al, 2006). MATEs have been implicated in anther dehiscence and pollen development (Thompson et al, 2010), plant architecture regulation (Li et al, 2014; Suzuki et al, 2015), root development (Upadhyay et al, 2020), organ initiation (Burko et al, 2011), and senescence (Jia et al, 2019)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call