Methyl jasmonate mediates melatonin-induced cold tolerance of grafted watermelon plants

Root–shoot communication has a critical role in plant adaptation to environmental stress. Grafting is widely applied to enhance the abiotic stress tolerance of many horticultural crop species; however, the signal transduction mechanism involved in this tolerance remains unknown. Here, we show that p...

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Veröffentlicht in:Horticulture research 2021-03, Vol.8 (1), p.57, Article 57
Hauptverfasser: Li, Hao, Guo, Yanliang, Lan, Zhixiang, Xu, Kai, Chang, Jingjing, Ahammed, Golam Jalal, Ma, Jianxiang, Wei, Chunhua, Zhang, Xian
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Sprache:eng
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Zusammenfassung:Root–shoot communication has a critical role in plant adaptation to environmental stress. Grafting is widely applied to enhance the abiotic stress tolerance of many horticultural crop species; however, the signal transduction mechanism involved in this tolerance remains unknown. Here, we show that pumpkin- or figleaf gourd rootstock-enhanced cold tolerance of watermelon shoots is accompanied by increases in the accumulation of melatonin, methyl jasmonate (MeJA), and hydrogen peroxide (H 2 O 2 ). Increased melatonin levels in leaves were associated with both increased melatonin in rootstocks and MeJA-induced melatonin biosynthesis in leaves of plants under cold stress. Exogenous melatonin increased the accumulation of MeJA and H 2 O 2 and enhanced cold tolerance, while inhibition of melatonin accumulation attenuated rootstock-induced MeJA and H 2 O 2 accumulation and cold tolerance. MeJA application induced H 2 O 2 accumulation and cold tolerance, but inhibition of JA biosynthesis abolished rootstock- or melatonin-induced H 2 O 2 accumulation and cold tolerance. Additionally, inhibition of H 2 O 2 production attenuated MeJA-induced tolerance to cold stress. Taken together, our results suggest that melatonin is involved in grafting-induced cold tolerance by inducing the accumulation of MeJA and H 2 O 2 . MeJA subsequently increases melatonin accumulation, forming a self-amplifying feedback loop that leads to increased H 2 O 2 accumulation and cold tolerance. This study reveals a novel regulatory mechanism of rootstock-induced cold tolerance.
ISSN:2662-6810
2052-7276
DOI:10.1038/s41438-021-00496-0