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Key message <p><i>GSH1</i> functions the downstream of <i>SNAT</i>-mediated melatonin in Cd tolerance, increasing glutathione and total PCs contents.</p> Abstract <p>Melatonin is a multifunctional signaling molecule involved in mitigating the damage caused by cadmium (Cd) stress in plants.&#xa0;Previous studies suggested that the gene encoding serotonin&#xa0;<i>N</i>-acetyltransferase (<i>SNAT</i>) was the key gene in the melatonin biosynthetic pathway. Besides, glutathione (GSH) contributed to plant Cd tolerance, however, the specific role of SNAT-mediated melatonin biosynthesis in regulating GSH-dependent pathway, and whether <i>GSH1</i> acts as an essential downstream effector, remain undefined. Here, we found that <i>SNAT</i> modulated the endogenous melatonin content and Cd stress response in Arabidopsis. Under Cd stress, <i>SNAT-</i>overexpressing roots accumulated higher melatonin levels and exhibited enhanced Cd tolerance with increased root elongation and fresh weight, whereas the <i>atsnat</i> mutant displayed reduced melatonin and hypersensitivity to Cd compared to wild-type. Furthermore, GSH levels were significantly higher in <i>SNAT</i>-overexpressing plants but not in the <i>atsnat</i> mutant upon Cd stress. Treatment with <i>L</i>-buthionine-(S,R)-sulfoximine (BSO, a GSH biosynthesis inhibitor), significantly decreased GSH levels across all genotypes. Exogenous melatonin failed to rescue Cd hypersensitivity in <i>GSH1</i> mutant <i>atcad2-1</i>, which was defective in GSH biosynthesis. Genetic and transcriptional analyses further confirmed that <i>GSH1</i> might be, at least partially, a downstream target of melatonin signaling to mediate Cd tolerance through GSH metabolism. Collectively, these findings highlight the critical role of the <i>GSH1</i>-mediated GSH accumulation in <i>SNAT</i>-dependent melatonin-enhanced plant tolerance to Cd stress. This advances current understanding by identifying <i>GSH1</i> as a critical node integrating melatonin and heavy metal tolerance pathways.</p>

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GSH1 plays a crucial role in melatonin-mediated cadmium tolerance in Arabidopsis

  • 期刊论文

  • 发表日期：

    2025年10月10日

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  • Quan Gu,
  • Yu Liu,
  • Longjiang Gu,
  • Chenyang Xie,
  • Wenyang Zhang,
  • Liji Du,
  • Qianqian Fu,
  • Ziping Chen,
  • Wenbiao Shen

摘要

Key message

GSH1 functions the downstream of SNAT-mediated melatonin in Cd tolerance, increasing glutathione and total PCs contents.

Abstract

Melatonin is a multifunctional signaling molecule involved in mitigating the damage caused by cadmium (Cd) stress in plants. Previous studies suggested that the gene encoding serotonin N-acetyltransferase (SNAT) was the key gene in the melatonin biosynthetic pathway. Besides, glutathione (GSH) contributed to plant Cd tolerance, however, the specific role of SNAT-mediated melatonin biosynthesis in regulating GSH-dependent pathway, and whether GSH1 acts as an essential downstream effector, remain undefined. Here, we found that SNAT modulated the endogenous melatonin content and Cd stress response in Arabidopsis. Under Cd stress, SNAT-overexpressing roots accumulated higher melatonin levels and exhibited enhanced Cd tolerance with increased root elongation and fresh weight, whereas the atsnat mutant displayed reduced melatonin and hypersensitivity to Cd compared to wild-type. Furthermore, GSH levels were significantly higher in SNAT-overexpressing plants but not in the atsnat mutant upon Cd stress. Treatment with L-buthionine-(S,R)-sulfoximine (BSO, a GSH biosynthesis inhibitor), significantly decreased GSH levels across all genotypes. Exogenous melatonin failed to rescue Cd hypersensitivity in GSH1 mutant atcad2-1, which was defective in GSH biosynthesis. Genetic and transcriptional analyses further confirmed that GSH1 might be, at least partially, a downstream target of melatonin signaling to mediate Cd tolerance through GSH metabolism. Collectively, these findings highlight the critical role of the GSH1-mediated GSH accumulation in SNAT-dependent melatonin-enhanced plant tolerance to Cd stress. This advances current understanding by identifying GSH1 as a critical node integrating melatonin and heavy metal tolerance pathways.