2012 Fiscal Year Final Research Report
Research on regulation and expression mechanisms of functionalglycans associated with congenital muscular dystrophy
Project/Area Number |
23659153
|
Research Category |
Grant-in-Aid for Challenging Exploratory Research
|
Allocation Type | Multi-year Fund |
Research Field |
General medical chemistry
|
Research Institution | Kyoto University |
Principal Investigator |
OKA Shogo 京都大学, 医学研究科, 教授 (60233300)
|
Co-Investigator(Renkei-kenkyūsha) |
KAWASAKI Nana 国立医薬品食品衛生研究所, 生物薬品部, 部長 (20186167)
|
Project Period (FY) |
2011 – 2012
|
Keywords | 生体分子医学 / 機能糖鎖 |
Research Abstract |
α-Dystroglycan undergoes extensive glycosylation required for the interaction between α-dystroglycan and the extracellular matrix such as laminin and aberrant glycosylation of α-DG has already been identified in the pathogenesis of several types of congenital muscular dystrophy. In this study, we revealed that a sulfotransferase, HNK-1ST, suppressed the glycosylation and reduced the ligand-binding activity of α-dystroglycan. We also found that HNK-1ST regulated the migration of melanoma cells through the glycosylation state on α-dystroglycan
|