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Vol. 11, Issue 9, 2901-2914, September 2000
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and
*Dipartimento di Scienze e Tecnologie Biomediche,
Sezione di Biologia, Universita' di Udine, 33100 Udine, Italy;
Gas3/PMP22 is a tetraspan membrane protein highly expressed
in myelinating Schwann cells. Point mutations in the
gas3/PMP22 gene account for the dominant
inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease
(CMT1A) and Dejerine-Sottas syndrome (DSS). Gas3/PMP22 can regulate
apoptosis and cell spreading in cultured cells.
Gas3/PMP22 point mutations, which are
responsible for these diseases, are defective in this respect. In this
report, we demonstrate that Gas3/PMP22-WT is exposed at the cell
surface, while its point-mutated derivatives are intracellularly
retained, colocalizing mainly with the endoplasmic reticulum
(ER). The putative retrieval motif present in the carboxyl
terminus of Gas3/PMP22 is not sufficient for the intracellular
sequestration of its point-mutated forms. On the contrary, the
introduction of a retrieval signal at the carboxyl terminus of
Gas3/PMP22-WT leads to its intracellular accumulation, which is
accompanied by a failure to trigger cell death as well as by changes in
cell spreading. In addition, by substituting the Asn at position 41 required for N-glycosylation, we provide evidence that N-glycosylation
is required for the full effect on cell spreading, but it is not
necessary for triggering cell death. In conclusion, we suggest that the
DSS and the CMT1A neuropathies derived from point mutations of
Gas3/PMP22 might arise, at the molecular
level, from a reduced exposure of Gas3/PMP22 at the cell surface, which
is required to exert its biological functions.
Laboratorio Nazionale Consorzio Interuniversitario
Biotecnologie AREA Science Park, Padriciano 99 34142 Trieste, Italy;
Dipartimento di Biologia Universita' di Trieste, 34100 Trieste, Italy
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