4.7 Article

Abscisic Acid Mediates Salicylic Acid Induced Chilling Tolerance of Grafted Cucumber by Activating H2O2 Biosynthesis and Accumulation

期刊

出版社

MDPI
DOI: 10.3390/ijms232416057

关键词

salicylic acid; abscisic acid; hydrogen peroxide; signal transduction chilling tolerance; cucumber; pumpkin

资金

  1. National Science Foundation of China [31872155]
  2. National Key Research and Development Program of China [2019YFD1000300]
  3. Special Fund of Vegetable Industrial Technology System of Shandong Province in China [SDAIT-05-10]
  4. Funds of Shandong Double Tops' Program [SYL2017YSTD06]

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This study revealed that grafting with pumpkin as a rootstock improved chilling tolerance in cucumber leaves. It increased the accumulation of salicylic acid, abscisic acid, and hydrogen peroxide. Salicylic acid participated in grafting-induced chilling tolerance by stimulating the biosynthesis of abscisic acid and hydrogen peroxide. Abscisic acid, as a downstream signaler of salicylic acid, mediated the salicylic acid-induced chilling tolerance in grafted cucumber plants.
Grafting is widely applied to enhance the tolerance of some vegetables to biotic and abiotic stress. Salicylic acid (SA) is known to be involved in grafting-induced chilling tolerance in cucumber. Here, we revealed that grafting with pumpkin (Cucurbita moschata, Cm) as a rootstock improved chilling tolerance and increased the accumulation of SA, abscisic acid (ABA) and hydrogen peroxide (H2O2) in grafted cucumber (Cucumis sativus/Cucurbita moschata, Cs/Cm) leaves. Exogenous SA improved the chilling tolerance and increased the accumulation of ABA and H2O2 and the mRNA abundances of CBF1, COR47, NCED, and RBOH1. However, 2-aminoindan-2-phosphonic acid (AIP) and L-a-aminooxy-b-phenylpropionic acid (AOPP) (biosynthesis inhibitors of SA) reduced grafting-induced chilling tolerance, as well as the synthesis of ABA and H2O2, in cucumber leaves. ABA significantly increased endogenous H2O2 production and the resistance to chilling stress, as proven by the lower electrolyte leakage (EL) and chilling injury index (CI). However, application of the ABA biosynthesis inhibitors sodium tungstate (Na2WO4) and fluridone (Flu) abolished grafting or SA-induced H2O2 accumulation and chilling tolerance. SA-induced plant response to chilling stress was also eliminated by N,N '-dimethylthiourea (DMTU, an H2O2 scavenger). In addition, ABA-induced chilling tolerance was attenuated by DMTU and diphenyleneiodonium (DPI, an H2O2 inhibitor) chloride, but AIP and AOPP had little effect on the ABA-induced mitigation of chilling stress. Na2WO4 and Flu diminished grafting- or SA-induced H2O2 biosynthesis, but DMTU and DPI did not affect ABA production induced by SA under chilling stress. These results suggest that SA participated in grafting-induced chilling tolerance by stimulating the biosynthesis of ABA and H2O2. H2O2, as a downstream signaler of ABA, mediates SA-induced chilling tolerance in grafted cucumber plants.

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