Source:http://linkedlifedata.com/resource/pubmed/id/17034757
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2006-10-23
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pubmed:abstractText |
The recent identification of mutations in genes encoding demonstrated or putative glycosyltransferases has revealed a novel mechanism for congenital muscular dystrophy. Hypoglycosylated alpha-dystroglycan (alpha-DG) is commonly seen in Fukuyama-type congenital muscular dystrophy (FCMD), muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Large(myd) mice. POMGnT1 and POMTs, the gene products responsible for MEB and WWS, respectively, synthesize unique O-mannose sugar chains on alpha-DG. The function of fukutin, the gene product responsible for FCMD, remains undetermined. Here we show that fukutin co-localizes with POMGnT1 in the Golgi apparatus. Direct interaction between fukutin and POMGnT1 was confirmed by co-immunoprecipitation and two-hybrid analyses. The transmembrane region of fukutin mediates its localization to the Golgi and participates in the interaction with POMGnT1. Y371C, a missense mutation found in FCMD, retains fukutin in the ER and also redirects POMGnT1 to the ER. Finally, we demonstrate reduced POMGnT1 enzymatic activity in transgenic knock-in mice carrying the retrotransposal insertion in the fukutin gene, the prevalent mutation in FCMD. From these findings, we propose that fukutin forms a complex with POMGnT1 and may modulate its enzymatic activity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DAG1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Dystroglycans,
http://linkedlifedata.com/resource/pubmed/chemical/Fcmd protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/N-Acetylglucosaminyltransferases,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/protein O-mannose...
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0006-291X
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pubmed:author |
pubmed-author:ChiyonobuTomohiroT,
pubmed-author:EndoTamaoT,
pubmed-author:FujikakeNobuhiroN,
pubmed-author:KanagawaMotoiM,
pubmed-author:KobayashiKazuhiroK,
pubmed-author:ManyaHiroshiH,
pubmed-author:MorrisGlenn EGE,
pubmed-author:NagaiYoshitakaY,
pubmed-author:NishimotoAkemiA,
pubmed-author:TachikawaMasajiM,
pubmed-author:TakedaSatoshiS,
pubmed-author:TodaTatsushiT,
pubmed-author:WangFanF,
pubmed-author:XiongHuiH
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
350
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
935-41
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pubmed:meshHeading |
pubmed-meshheading:17034757-Animals,
pubmed-meshheading:17034757-COS Cells,
pubmed-meshheading:17034757-Cercopithecus aethiops,
pubmed-meshheading:17034757-Dystroglycans,
pubmed-meshheading:17034757-Glycosylation,
pubmed-meshheading:17034757-Humans,
pubmed-meshheading:17034757-Mice,
pubmed-meshheading:17034757-N-Acetylglucosaminyltransferases,
pubmed-meshheading:17034757-Protein Binding,
pubmed-meshheading:17034757-Protein Interaction Mapping,
pubmed-meshheading:17034757-Proteins,
pubmed-meshheading:17034757-Signal Transduction
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pubmed:year |
2006
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pubmed:articleTitle |
Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan.
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pubmed:affiliation |
Division of Clinical Genetics, Department of Medical Genetics, Osaka University Graduate School of Medicine, 2-2-B9 Yamadaoka, Suita, Osaka 565-0871, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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