# Melatonin at Crossroads with Phytohormones: Interactions Under High Light Stress

## TL;DR

This study explores how melatonin interacts with plant hormones under high light stress, revealing new insights into its role in stress response and growth regulation.

## Contribution

The study identifies specific gene expression patterns and signaling pathways modulated by melatonin under high light stress.

## Key findings

- Melatonin activates auxin and brassinosteroid response genes while suppressing abscisic acid and ethylene signaling.
- Melatonin enhances gibberellin and cytokinin gene expression, aiding stress alleviation.
- The MAP3K17-MKK7 module is crucial in melatonin-triggered signaling downstream of CAND2.

## Abstract

Melatonin (MT), an antioxidant and growth regulator, interacts with almost all phytohormones, but the molecular mechanisms of these interactions are poorly understood. Using mRNA sequencing (mRNA-seq) technology, we analysed the global regulation of MT-induced expression of genes involved in metabolism, signalling and responses to major phytohormones under prolonged high-intensity light (HL) stress. Plants respond to MT through the activation of auxin and brassinosteroid (BS) response genes, which were identified among the enriched categories of differentially expressed genes (DEGs) with increased expression, and the suppression of abscisic acid and ethylene signalling and response genes, which were among the enriched downregulated categories. MT also suppressed growth-inhibiting genes involved in jasmonic acid (JA) and salicylic acid (SA) signalling and response and activated genes encoding the growth-promoting hormones gibberellins and cytokinins (CKs), which is consistent with the role of MT in stress alleviation. However, the expression of some unique genes, which are positively or negatively modulated by stress, was reinforced by MT treatment, illustrating the extraordinary type of regulation that enhances the action of specific hormone-mediated mechanisms. The study of signal integration between MT and hormones with the involvement of signalling mutants revealed that some interactions are regulated at the transcriptional level and require the activity of relevant signalling pathways. Disruption of CAND2 completely abolished melatonin-dependent activation of the mitogen-activated protein kinases MAP3K17 and MKK7, suggesting that the MAP3K17-MKK7 module is an important player in the MT-triggered MAPK pathway, acting downstream of CAND2.