MsMIOX2, encoding a MsbZIP53‐activated myo‐inositol oxygenase, enhances saline–alkali stress tolerance by regulating cell wall pectin and hemicellulose biosynthesis in alfalfa

半纤维素 化学 果胶 生理盐水 生物化学 细胞生物学 生物 内分泌学 纤维素
作者
Weileng Guo,Jiaxin Chen,Lei Liu,Yuekun Ren,Rui Guo,Jing Wang,Jia Li,Jang Heui Chai,Yang Sun,Changhong Guo
出处
期刊:Plant Journal [Wiley]
标识
DOI:10.1111/tpj.17032
摘要

SUMMARY Alfalfa is one of the most widely cultivated forage crops worldwide. However, soil salinization restricts alfalfa growth and development and affects global productivity. The plant cell wall is the first barrier against various stresses. Therefore, elucidating the alterations in cell wall architecture is crucial for stress adaptation. This study aimed to clarify the impact of myo‐inositol oxygenase 2 (MsMIOX2) on cell wall pectin and hemicellulose biosynthesis under saline–alkali stress and identify the upstream transcription factors that govern MsMIOX2 . MsMIOX2 activation induced cell wall pectin and hemicellulose accumulation under saline–alkali stress. The effects of MsMIOX2 in saline–alkali tolerance were investigated by characterizing its overexpression and RNA interference lines. MsMIOX2 overexpression positively regulated the antioxidant system and photosynthesis in alfalfa under saline–alkali stress. MsMIOX2 exhibited myo‐inositol oxygenase activity, which increased polysaccharide contents, facilitated pectin and hemicellulose biosynthesis, and extended the cell wall thickness. However, MsMIOX2 RNA interference decreased cell wall thickness and alleviated alfalfa saline–alkali stress tolerance. In addition, MsbZIP53 was identified as an upstream transcriptional MsMIOX2 regulator by yeast one‐hybrid, electrophoretic mobility shift assay, dual‐luciferase, and beta‐glucuronidase assays. MsbZIP53 overexpression increased MsMIOX2 expression, elevated MIOX activity, reinforced the antioxidant system and photosynthesis, and increased saline–alkali stress tolerance in alfalfa. In conclusion, this study presents a novel perspective for elucidating the molecular mechanisms of saline–alkali stress tolerance in alfalfa and emphasizes the potential use of MsMIOX2 in alfalfa breeding.
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