4.7 Article

Applying transcriptomics to study glycosylation at the cell type level

期刊

ISCIENCE
卷 25, 期 6, 页码 -

出版社

CELL PRESS
DOI: 10.1016/j.isci.2022.104419

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资金

  1. Lundbeck Foundation [R223-2016-563]
  2. Novo Nordisk Foundation [NNF21OC0071658]
  3. Danish National Research Foundation [DNRF107]

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This study investigates the state of glycosylation machinery and metabolic network in a single cell using single cell RNA-seq data. The research reveals that most of the protein and lipid oligosaccharide scaffolds are produced by enzymes with limited transcriptional regulation among cells. Key enzymes within different glycosylation pathways are predicted to be highly transcriptionally regulated.
The complex multi-step process of glycosylation occurs in a single cell, yet current analytics generally cannot measure the output (the glycome) of a single cell. Here, we addressed this discordance by investigating how single cell RNA-seq data can be used to characterize the state of the glycosylation machinery and metabolic network in a single cell. The metabolic network involves 214 glycosylation and modification enzymes outlined in our previously built atlas of cellular glycosylation pathways. We studied differential mRNA regulation of enzymes at the organ and single cell level, finding that most of the general protein and lipid oligosaccharide scaffolds are produced by enzymes exhibiting limited transcriptional regulation among cells. We predict key enzymes within different glycosylation pathways to be highly transcriptionally regulated as regulatable hotspots of the cellular glycome. We designed the Glycopacity software that enables investigators to extract and interpret glycosylation information from transcriptome data and define hotspots of regulation.

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