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Elucidating Human Milk Oligosaccharide biosynthetic genes through network-based multi-omics integration.

Nature communications | 2022

Human Milk Oligosaccharides (HMOs) are abundant carbohydrates fundamental to infant health and development. Although these oligosaccharides were discovered more than half a century ago, their biosynthesis in the mammary gland remains largely uncharacterized. Here, we use a systems biology framework that integrates glycan and RNA expression data to construct an HMO biosynthetic network and predict glycosyltransferases involved. To accomplish this, we construct models describing the most likely pathways for the synthesis of the oligosaccharides accounting for >95% of the HMO content in human milk. Through our models, we propose candidate genes for elongation, branching, fucosylation, and sialylation of HMOs. Our model aggregation approach recovers 2 of 2 previously known gene-enzyme relations and 2 of 3 empirically confirmed gene-enzyme relations. The top genes we propose for the remaining 5 linkage reactions are consistent with previously published literature. These results provide the molecular basis of HMO biosynthesis necessary to guide progress in HMO research and application with the goal of understanding and improving infant health and development.

Pubmed ID: 35508452 RIS Download

Research resources used in this publication

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Antibodies used in this publication

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Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R21 HD080682
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM130915
  • Agency: NIGMS NIH HHS, United States
    Id: P41 GM103390
  • Agency: NIGMS NIH HHS, United States
    Id: P01 GM107012
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM119850

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