# Transcriptome and metabolite profiles reveal differential molecular responses of wild and cultivated amaranth species to water deficit and salt stress

**Authors:** Ana P. Barba de la Rosa, Jose Cetz, Esaú Bojórquez-Velázquez, José P. Martínez, Antonio De León-Rodríguez, Eduardo Espitia-Rangel, Alfredo Herrera-Estrella

PMC · DOI: 10.1007/s00425-026-04927-x · 2026-01-29

## TL;DR

This study compares how wild and cultivated amaranth species respond to drought and salt stress at the molecular level, revealing differences in gene expression and metabolism.

## Contribution

The study identifies distinct transcriptomic and metabolomic responses in wild and cultivated amaranth under abiotic stress.

## Key findings

- A. hybridus shows constitutive salinity tolerance linked to phosphonate and steroid metabolism.
- A. hypochondriacus responds to salt stress with increased ABC transporters and metabolism of sugars and amino acids.
- Both species adjust cell wall and defense-related metabolism under stress.

## Abstract

A. hybridus tolerance to salinity depends on constitutively active mechanisms, whereas A. hypochondriacus tolerance to salt and water deficit depends on a constitutive protection and a robust transcriptional response.

Drought and soil salinity are two environmental factors that significantly affect crop production. To gain a better understanding of how amaranth responds to these abiotic stresses, we analyzed the transcriptomic and metabolomic changes in the leaves of Amaranthus hybridus, a wild species, and A. hypochondriacus, a cultivated species used for seed production. We identified differentially expressed genes (DEGs) between the two species and under different stress conditions. Control plants of A. hypochondriacus exhibited higher expression levels of genes associated with photosynthesis, amino acid metabolism, fatty acid metabolism, sulfur metabolism, thiamine metabolism, and secondary metabolism. Notably, A. hybridus under salt stress showed an up-regulation of genes related to phosphonate and phosphinate metabolism and steroid biosynthesis. In contrast, the response of A. hypochondriacus to salt stress was characterized by increased expression of ABC transporters and genes involved in fructose, mannose, trehalose, porphyrin, thiamine, and monoterpenoid metabolism. When subjected to both types of stresses, A. hypochondriacus showed up-regulation of MAPK signaling pathways, ABC transporters, galactose, branched-chain amino acid (BCAA) degradation, and the production of defense compounds. Both amaranth species modulated their metabolic processes in response to drought and salinity stress towards cell wall modification, as well as the metabolism of pectin and lignin, while also producing antimicrobial and antifungal metabolites. Additionally, we detected differential accumulation of compounds, including methylphosphonate, 2-hydroxyethylphosphonate, and several metabolites related to fatty acid metabolism in the leaves of both amaranth species.

The online version contains supplementary material available at 10.1007/s00425-026-04927-x.

## Linked entities

- **Chemicals:** methylphosphonate (PubChem CID 14671056), 2-hydroxyethylphosphonate (PubChem CID 89954)
- **Species:** Amaranthus hybridus (taxon 3565)

## Full-text entities

- **Genes:** SHM4 (serine hydroxymethyltransferase 4) [NCBI Gene 827027] {aka DL3005C, FCAALL.160, SERINE HYDROXYMETHYLTRANSFERASE 4, serine hydroxymethyltransferase 4}, LOX6 (PLAT/LH2 domain-containing lipoxygenase family protein) [NCBI Gene 843077] {aka ATLOX6, Arabidopsis thaliana lipoxygenase 6, F12B7.11, F12B7_11, lipoxygenase 6}
- **Diseases:** hypoxia (MESH:D000860), impaired chlorophyll biosynthesis (OMIM:610293), Water deficit (MESH:D000069578), drought (MESH:C536747), stunted plants (MESH:D006130), Chlorosis (MESH:D000747), iron (Fe) deficiency (MESH:D000090463)
- **Chemicals:** sulfite (MESH:D013447), water (MESH:D014867), H2O2 (MESH:D006861), Trehalose (MESH:D014199), NaCl (MESH:D012965), alpha-tocopherol (MESH:D024502), alanine (MESH:D000409), polysaccharides (MESH:D011134), N-hexadecanoic acid (MESH:D019308), proline (MESH:D011392), pantothenic acid (MESH:D010205), GA (MESH:D005707), malondialdehyde (MESH:D008315), hypotaurine (MESH:C003949), carbonate (MESH:D002254), sulfur compound (MESH:D013457), Phytol (MESH:D010836), chlorophyll (MESH:D002734), glycerophospholipid (MESH:D020404), cholesterol (MESH:D002784), campesterol (MESH:C021273), selenium (MESH:D012643), CO2 (MESH:D002245), mannose (MESH:D008358), Flavonoid (MESH:D005419), chlorophyll b (MESH:C037184), nicotiflorin (MESH:C513882), steroid (MESH:D013256), aspartate (MESH:D001224), Phosphinic acid (MESH:D010721), beta -Alanine (MESH:D015091), Helium (MESH:D006371), ROS (MESH:D017382), nicotinate (MESH:D009525), sucrose (MESH:D013395), starch (MESH:D013213), carbohydrate (MESH:D002241), taurine (MESH:D013654), methylphosphonate (MESH:C032627), oxylipins (MESH:D054883), coenzyme A (MESH:D003065), terpene (MESH:D013729), acid (MESH:D000143), GABA (MESH:D005680), auxin (MESH:D007210), ethanol (MESH:D000431), Sterols (MESH:D013261), Quercetin (MESH:D011794), carbon (MESH:D002244), phosphate (MESH:D010710), dicarboxylic acid (MESH:D003998), essential amino acids (MESH:D000601), porphyrin (MESH:D011166), Biotin (MESH:D001710), BCAA (MESH:D000597), glycine (MESH:D005998), phosphorus (MESH:D010758), lignin (MESH:D008031), reactive nitrogen species (MESH:D026361), glyoxylate (MESH:C031150)
- **Species:** Amaranthus hybridus (green amaranth, species) [taxon 3565], Amaranthus caudatus (amaranth, species) [taxon 3567], Amaranthus (genus) [taxon 3564], Amaranthus hypochondriacus (grain amaranth, species) [taxon 28502], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12855421/full.md

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Source: https://tomesphere.com/paper/PMC12855421