生物
糖生物学
糖基化
聚糖
核糖核酸
细胞生物学
唾液酸
岩藻糖
糖蛋白
生物化学
基因
作者
Ryan A. Flynn,Kayvon Pedram,Stacy A. Malaker,Pedro J. Batista,Benjamin Smith,Alex G. Johnson,Benson M. George,Karim Majzoub,Peter W. Villalta,Jan E. Carette,Carolyn R. Bertozzi
出处
期刊:Cell
[Elsevier]
日期:2021-05-17
卷期号:184 (12): 3109-3124.e22
被引量:336
标识
DOI:10.1016/j.cell.2021.04.023
摘要
Glycans modify lipids and proteins to mediate inter- and intramolecular interactions across all domains of life. RNA is not thought to be a major target of glycosylation. Here, we challenge this view with evidence that mammals use RNA as a third scaffold for glycosylation. Using a battery of chemical and biochemical approaches, we found that conserved small noncoding RNAs bear sialylated glycans. These “glycoRNAs” were present in multiple cell types and mammalian species, in cultured cells, and in vivo. GlycoRNA assembly depends on canonical N-glycan biosynthetic machinery and results in structures enriched in sialic acid and fucose. Analysis of living cells revealed that the majority of glycoRNAs were present on the cell surface and can interact with anti-dsRNA antibodies and members of the Siglec receptor family. Collectively, these findings suggest the existence of a direct interface between RNA biology and glycobiology, and an expanded role for RNA in extracellular biology.
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