Transcriptomic and physiological analyses revealed the effects of exogenous MeJA on the antioxidant system and hormone signaling network in apple roots (Malus baccata L.) in response to suboptimal low root-zone temperature stress
Ping Dai , Yilu Zhao , Aiguo Wang , Huafeng Li , Deguo Lyu , Huaiyu Ma
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引用次数: 0
Abstract
Low temperature limits the growth and yield of apple trees. Previous experiments have proven that exogenous methyl jasmonate (MeJA) can improve the low-temperature adaptability in Malus baccata Borkh. roots which is widely used as rootstocks in northern China. Whereas the molecular mechanism of MeJA regulating the suboptimal low-temperature adaptability of apple roots remain poorly understood. The purpose of this work was to explore the potential regulating mechanisms of jasmonate signal in M. baccata roots in response to suboptimal low root-zone temperature stress (5 ± 0.5 °C for 2 h) through transcriptome and physiological analysis. Transcriptome bioinformatics analyses demonstrated that 2285 differentially expressed genes (DEGs) were predominantly associated with the jasmonates biosynthesis, hormone signaling pathways, MAPK signaling, and glutathione metabolism. Further investigations highlighted the regulating role of JAs in the low-temperature acclimation of the apple roots. Firstly, MeJA application inhibited the accumulations of reactive oxygen species and malondialdehyde in M. baccata roots through increasing antioxidant enzyme activities under suboptimal low-temperature, together with the increase of endogenous JAs levels. Secondly, the transcriptional levels of several pivotal JAs signaling genes were significantly up-regulated in the MeJA pre-treated roots under suboptimal low-temperature, verified through expression profiling and qRT-PCR analyses. Thirdly, MbMYC2 directly bound to the promoter of MbPOD, encoding a transcription factor involved in the antioxidant system, and enhanced its transcription. In summary, the mechanism of MeJA enhancing the antioxidant adaptability of M. baccata roots under suboptimal low-temperature stress has been preliminarily clarified, which provides new insights for further elaboration of molecular mechanism that are involved in low-temperature adaptability of apple roots.
期刊介绍:
The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues.
Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and:
Lack of water (drought) and excess (flooding),
Salinity stress,
Elevated temperature and/or low temperature (chilling and freezing),
Hypoxia and/or anoxia,
Mineral nutrient excess and/or deficiency,
Heavy metals and/or metalloids,
Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection,
Viral, phytoplasma, bacterial and fungal plant-pathogen interactions.
The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.