The Identification of MATE Antisense Transcripts in Soybean Using Strand-Specific RNA-Seq Datasets

Natural antisense transcripts (NATs) have been generally reported as negative regulators of their sense counterparts. Multidrug and toxic compound extrusion (MATE) proteins mediate the transport of various substrates. Although MATEs have been identified genome-wide in various plant species, their transcript regulators remain unclear. Here, using the publicly available strand-specific RNA-seq datasets of Glycine soja (wild soybean) which have the data from various tissues including developing pods, developing seeds, embryos, cotyledons and hypocotyls, roots, apical buds, stems, and flowers, we identified 35 antisense transcripts of MATEs from 28 gene loci after transcriptome assembly. Spearman correlation coefficients suggested the positive expression correlations of eight MATE antisense and sense transcript pairs. By aligning the identified transcripts with the reference genome of Glycine max (cultivated soybean), the MATE antisense and sense transcript pairs were identified. Using soybean C08 (Glycine max), in developing pods and seeds, the positive correlations between MATE antisense and sense transcript pairs were shown by RT-qPCR. These findings suggest that soybean antisense transcripts are not necessarily negative transcription regulators of their sense counterparts. This study enhances the existing knowledge on the transcription regulation of MATE transporters by uncovering the previously unknown MATE antisense transcripts and their potential synergetic effects on sense transcripts.

Automated summary

This study identified 35 antisense transcripts of multidrug and toxic compound extrusion (MATE) proteins in Glycine soja using RNA-seq datasets. Positive expression correlations were found between eight antisense and sense transcript pairs. RT-qPCR confirmed the positive correlations between MATE antisense and sense transcript pairs in developing pods and seeds of soybean. These findings suggest that soybean antisense transcripts may not necessarily act as negative regulators of their sense counterparts. This study enhances our understanding of the transcription regulation of MATE transporters.