Trends in Glycoscience and Glycotechnology
Online ISSN : 1883-2113
Print ISSN : 0915-7352
ISSN-L : 0915-7352
Article for JSCR 40th Anniversary Issue
Mechanisms of O-Mannosyl Glycan Biosynthesis in Mammals
Hiroshi Manya
Author information
JOURNALS RESTRICTED ACCESS

2019 Volume 31 Issue 181 Pages SE63-SE64

Details
Abstract

We previously reported that a defect in O-mannosyl glycan is the primary cause of a group of congenital muscular dystrophies. Based on our pioneering findings, numerous studies have been performed and revealed various structures of O-mannosyl glycans. However, the glycan structure associated with muscular dystrophies remained unclear for a long time. Recently, we described the complete structure of an O-mannosyl glycan containing ribitol-phosphate (RboP), which had not previously been identified as a glycan component in mammals. In addition, its unique biosynthetic pathway was elucidated by identifying the functions of the gene products associated with muscular dystrophies. Here, we review recent findings regarding the mechanisms of O-mannosyl glycan biosynthesis in mammals.

Information related to the author
© 2019 FCCA (Forum: Carbohydrates Coming of Age)
Previous article Next article
feedback
Top