4.6 Article

Dendrobium Multi-Omics Reveal Lipid Remodeling in Response to Freezing

期刊

METABOLITES
卷 12, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/metabo12121216

关键词

Dendrobium; lipidome; proteome; cold stress

资金

  1. National Natural Science Foundation of China
  2. [32200304]

向作者/读者索取更多资源

This study used a multi-omics strategy to investigate the metabolic flow during freezing treatment and post-freezing recovery in Dendrobium catenatum. Proteome and lipidome assays revealed significant remodeling in the phospholipid category and upregulation of most sphingolipids during freezing. Integrated multi-omics analysis identified significant changes in the expression levels of mRNAs and encoding proteins associated with phospholipid editing and galactolipid remodeling. These findings provide insights into improving the freezing tolerance of D. catenatum through genetic engineering.
Freezing damage is a common phenomenon responsible for reduced yields of economic crops. Regulation of lipid metabolism plays an important role in plant growth and adaptation during freezing. We previously carried out transcriptome and untargeted metabolome analyses to determine the regulation of flavonol and anthocyanin biosynthesis during freezing treatment (FT) and post-freezing recovery (FR) in Dendrobium catenatum. However, changes in lipid levels are hard to confirm by untargeted metabolomics analysis alone. Regulation of lipid metabolism in response to freezing is largely unknown in Dendrobium. In this study, a multi-omics strategy was used to offer a better means of studying metabolic flow during FT and FR. To this end, 6976 proteins were identified by the 4D_label-free proteome, including 5343 quantified proteins. For each of the two conditions, we enriched differentially accumulated proteins (DAPs) into 15 gene ontology (GO) terms, including primary metabolism, lipid metabolism, and photosynthesis processes. We also identified 7 lipid categories and 3672 lipid species using lipidome assays. We found significant remodeling occurring in the phospholipid category during FT and FR. We also found that most sphingolipids were significantly upregulated. An integrated multi-omics analysis revealed significant changes in the expression levels of 141 mRNAs and encoding proteins under both FT and FR conditions. During FT, phospholipase A (PLA) and phospholipase D (PLD) were associated with phospholipid editing and galactolipid remodeling. These results provide valuable new insights into how the freezing tolerance of D. catenatum might be improved by genetic engineering.

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