4.7 Article

Analysis of Thioredoxins and Glutaredoxins in Soybean: Evidence of Translational Regulation under Water Restriction

Journal

ANTIOXIDANTS
Volume 11, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/antiox11081622

Keywords

Glycine max; thioredoxin; glutaredoxin; drought; transcriptome; translatome; root

Funding

  1. CSIC I+D 2020 [282]
  2. FVF 2017 [210]
  3. Programa de Desarrollo de las Ciencias Basicas (PEDECIBA), Red Nacional de Biotecnologia Agicola [RTS_1_2014_1-ANII]

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Soybean plants establish symbiosis with rhizobacteria to perform biological nitrogen fixation (BNF). This study investigated the differential response of nodulated soybean plants to water-deficit stress and identified a greater number of differentially expressed genes (DEGs) under water deficit compared to nodulation condition. Additionally, the complete repertoire of thioredoxins (Trx) and glutaredoxins (Grx) in soybean was identified, and a network involving their interaction with nitrogen metabolism enzymes was revealed.
Soybean (Glycine max (L.) Merr.) establishes symbiosis with rhizobacteria, developing the symbiotic nodule, where the biological nitrogen fixation (BNF) occurs. The redox control is key for guaranteeing the establishment and correct function of the BNF process. Plants have many antioxidative systems involved in ROS homeostasis and signaling, among them a network of thio- and glutaredoxins. Our group is particularly interested in studying the differential response of nodulated soybean plants to water-deficit stress. To shed light on this phenomenon, we set up an RNA-seq experiment (for total and polysome-associated mRNAs) with soybean roots comprising combined treatments including the hydric and the nodulation condition. Moreover, we performed the initial identification and description of the complete repertoire of thioredoxins (Trx) and glutaredoxins (Grx) in soybean. We found that water deficit altered the expression of a greater number of differentially expressed genes (DEGs) than the condition of plant nodulation. Among them, we identified 12 thioredoxin (Trx) and 12 glutaredoxin (Grx) DEGs, which represented a significant fraction of the detected GmTrx and GmGrx in our RNA-seq data. Moreover, we identified an enriched network in which a GmTrx and a GmGrx interacted with each other and associated through several types of interactions with nitrogen metabolism enzymes.

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