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连接糖组学与基因组学:功能遗传学在细胞糖基化研究中的新应用

Bridging Glycomics and Genomics: New Uses of Functional Genetics in the Study of Cellular Glycosylation.

作者信息

Stewart Natalie, Wisnovsky Simon

机构信息

Biochemistry and Microbiology Dept, University of Victoria, Victoria, BC, Canada.

Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada.

出版信息

Front Mol Biosci. 2022 Jun 16;9:934584. doi: 10.3389/fmolb.2022.934584. eCollection 2022.

Abstract

All living cells are coated with a diverse collection of carbohydrate molecules called glycans. Glycans are key regulators of cell behavior and important therapeutic targets for human disease. Unlike proteins, glycans are not directly templated by discrete genes. Instead, they are produced through multi-gene pathways that generate a heterogenous array of glycoprotein and glycolipid antigens on the cell surface. This genetic complexity has sometimes made it challenging to understand how glycosylation is regulated and how it becomes altered in disease. Recent years, however, have seen the emergence of powerful new functional genomics technologies that allow high-throughput characterization of genetically complex cellular phenotypes. In this review, we discuss how these techniques are now being applied to achieve a deeper understanding of glyco-genomic regulation. We highlight specifically how methods like ChIP-seq, RNA-seq, CRISPR genomic screening and scRNA-seq are being used to map the genomic basis for various cell-surface glycosylation states in normal and diseased cell types. We also offer a perspective on how emerging functional genomics technologies are likely to create further opportunities for studying cellular glycobiology in the future. Taken together, we hope this review serves as a primer to recent developments at the glycomics-genomics interface.

摘要

所有活细胞都被一层称为聚糖的多种碳水化合物分子所覆盖。聚糖是细胞行为的关键调节因子,也是人类疾病重要的治疗靶点。与蛋白质不同,聚糖不是由离散基因直接模板化产生的。相反,它们是通过多基因途径产生的,这些途径在细胞表面生成一系列异质性的糖蛋白和糖脂抗原。这种遗传复杂性有时使得理解糖基化如何被调控以及它在疾病中如何发生改变具有挑战性。然而,近年来出现了强大的新功能基因组学技术,这些技术能够对遗传复杂的细胞表型进行高通量表征。在这篇综述中,我们讨论了这些技术现在如何被应用以更深入地理解糖基因组调控。我们特别强调了诸如染色质免疫沉淀测序(ChIP-seq)、RNA测序(RNA-seq)、CRISPR基因组筛选和单细胞RNA测序(scRNA-seq)等方法如何被用于绘制正常和患病细胞类型中各种细胞表面糖基化状态的基因组基础。我们还对新兴的功能基因组学技术未来如何可能为研究细胞糖生物学创造更多机会提供了一个观点。总之,我们希望这篇综述能作为糖组学与基因组学交叉领域最新进展的入门介绍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b8b/9243437/d731b86d9574/fmolb-09-934584-g001.jpg

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