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Hum Genet ; 133(5): 599-616, 2014 May.
Article in English | MEDLINE | ID: mdl-24281389

ABSTRACT

Collagen Q (ColQ) is a key multidomain functional protein of the neuromuscular junction (NMJ), crucial for anchoring acetylcholinesterase (AChE) to the basal lamina (BL) and accumulating AChE at the NMJ. The attachment of AChE to the BL is primarily accomplished by the binding of the ColQ collagen domain to the heparan sulfate proteoglycan perlecan and the COOH-terminus to the muscle-specific receptor tyrosine kinase (MuSK), which in turn plays a fundamental role in the development and maintenance of the NMJ. Yet, the precise mechanism by which ColQ anchors AChE at the NMJ remains unknown. We identified five novel mutations at the COOH-terminus of ColQ in seven patients from five families affected with endplate (EP) AChE deficiency. We found that the mutations do not affect the assembly of ColQ with AChE to form asymmetric forms of AChE or impair the interaction of ColQ with perlecan. By contrast, all mutations impair in varied degree the interaction of ColQ with MuSK as well as basement membrane extract (BME) that have no detectable MuSK. Our data confirm that the interaction of ColQ to perlecan and MuSK is crucial for anchoring AChE to the NMJ. In addition, the identified COOH-terminal mutants not only reduce the interaction of ColQ with MuSK, but also diminish the interaction of ColQ with BME. These findings suggest that the impaired attachment of COOH-terminal mutants causing EP AChE deficiency is in part independent of MuSK, and that the COOH-terminus of ColQ may interact with other proteins at the BL.


Subject(s)
Acetylcholinesterase/genetics , Basement Membrane/metabolism , Collagen/genetics , Membrane Proteins/metabolism , Muscle Proteins/genetics , Mutation , Myasthenic Syndromes, Congenital/genetics , Acetylcholinesterase/metabolism , Animals , Base Sequence , COS Cells , Chlorocebus aethiops , Chromatography, Liquid , Collagen/metabolism , DNA Primers , HEK293 Cells , Humans , Muscle Proteins/metabolism , Protein Binding , Reverse Transcriptase Polymerase Chain Reaction , Tandem Mass Spectrometry
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