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Rewiring enervated : Thinking LARGEr than myodystrophy
Author(s) -
Levedakou Eleni N.,
Popko Brian
Publication year - 2006
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.20896
Subject(s) - mutant , dystroglycan , transgene , biology , phenotype , gene , muscular dystrophy , microbiology and biotechnology , schwann cell , dystrophin , glycoprotein , mutation , regeneration (biology) , neuroscience , genetics , extracellular matrix , laminin
LARGE is a glycosyltransferase known to glycosylate α‐dystroglycan, a component of the dystrophin‐associated glycoprotein complex. Spontaneous deletions in the Large gene ( Large myd and Large vls ) result in muscular dystrophy accompanied by heart, brain, and eye defects. Another Large mouse mutant, enervated ( Large enr ), is the result of a transgene integration event that disrupts Large gene expression. In addition to myodystrophy, enr mice have been shown to display peripheral nerve abnormalities, including altered axonal sorting resulting from Schwann cell defects, poor regeneration after nerve injury, and abnormal neuromuscular junctions. These data have provided new insight into our understanding of the function of LARGE and have suggested the possibility of involvement of substrates in addition to α‐dystroglycan in the generation of the LARGE phenotype. The Large mutants are excellent models for addressing the importance of glycosylation in neuromuscular disease. © 2006 Wiley‐Liss, Inc.