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J Biol Chem, Vol. 274, Issue 12, 8240-8246, March 19, 1999
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From the We have demonstrated previously 1) that the
dystroglycan complex, but not the sarcoglycan complex, is expressed in
peripheral nerve, and 2) that
Department of Neurology and Neuroscience,
Teikyo University School of Medicine, Tokyo 173-8605, Japan, the
§ Third Department of Internal Medicine, National Defense
Medical College, Saitama 359-8513, Japan, and the
¶ University School of Neuroscience and Muscular Dystrophy Group
Laboratories, Regional Neuroscience Centre, Newcastle General Hospital,
Newcastle-upon-Tyne NE4 6BE, United Kingdom
-dystroglycan is an extracellular
laminin-2-binding protein anchored to
-dystroglycan in the Schwann
cell membrane. In the present study, we investigated the transmembrane
molecular architecture of the dystroglycan complex in Schwann cells.
The cytoplasmic domain of
-dystroglycan was co-localized with Dp116, the Schwann cell-specific isoform of dystrophin, in the abaxonal Schwann cell cytoplasm adjacent to the outer membrane.
-dystroglycan bound to Dp116 mainly via the 15 C-terminal amino acids of its cytoplasmic domain, but these amino acids were not solely responsible for the interaction of these two proteins. Interestingly, the
-dystroglycan-precipitating antibody precipitated only a small fraction of
-dystroglycan and did not precipitate laminin and Dp116
from the peripheral nerve extracts. Our results indicate 1) that Dp116
is a component of the submembranous cytoskeletal system that anchors
the dystroglycan complex in Schwann cells, and 2) that the dystroglycan
complex in Schwann cells is fragile compared with that in striated
muscle cells. We propose that this fragility may be attributable to the
absence of the sarcoglycan complex in Schwann cells.
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