P0 constitutes 50-60% of protein in peripheral nerve myelin and is essential for its structure and stability. Mutations within the P0 gene (MPZ) underlie a variety of hereditary neuropathies. MpzS63C transgenic mice encode a P0 with a serine to cysteine substitution at position 34 in the extracellular domain of mature P0 (P0S34C), associated with the hypomyelinating Dejerine-Sottas syndrome in human. S63C mice develop a dysmyelinating neuropathy, with packing defects in peripheral myelin. Here, we used x-ray diffraction to examine time-dependent packing defects in unfixed myelin. At similar to 7 h post-dissection, WT and S63C(+/+) myelin showed native periods (175 angstrom) with the latter developing at most a few percent swollen myelin, whereas up to similar to 50% of S63C(+/-) (mutant P0 on heterozygous P0 null background) or P0(+/+) myelin swelled to periods of similar to 205 angstrom. In the same time frame, S63C(-/-) myelin was stable, remaining swollen at similar to 210 angstrom. Surprisingly, treatment of whole S63C(-/-) nerves with a reducing agent completely reverted swollen arrays to native spacing and also normalized the swollen arrays that had formed in S63C(+/-) myelin, the genotype most closely related to the human disorder. Western blot revealed P0-positive bands at similar to 27 and similar to 50 kDa, and MALDI-TOF mass spectrometry showed these bands consisted of Ser(34)-containing peptides or P0 dimers having oxidized Cys(34) residues. We propose that P0S34C forms ectopic disulfide bonds in trans between apposed Cys(34) side chains that retard wrapping during myelin formation causing hypomyelination. Moreover, the new bonds create a packing defect by stabilizing swollen membrane arrays that leads to demyelination.

P0 (Protein Zero) Mutation S34C Underlies Instability of Internodal Myelin in S63C Mice / L. Avila Robin, M. D'Antonio, A. Bachi, H. Inouye, M. Feltri, L. Wrabetz, A. Kirschner Daniel. - In: THE JOURNAL OF BIOLOGICAL CHEMISTRY. - ISSN 0021-9258. - 285:53(2010), pp. 42001-42012. [10.1074/jbc.M110.166967]

P0 (Protein Zero) Mutation S34C Underlies Instability of Internodal Myelin in S63C Mice

M. Feltri
Membro del Collaboration Group
;
2010

Abstract

P0 constitutes 50-60% of protein in peripheral nerve myelin and is essential for its structure and stability. Mutations within the P0 gene (MPZ) underlie a variety of hereditary neuropathies. MpzS63C transgenic mice encode a P0 with a serine to cysteine substitution at position 34 in the extracellular domain of mature P0 (P0S34C), associated with the hypomyelinating Dejerine-Sottas syndrome in human. S63C mice develop a dysmyelinating neuropathy, with packing defects in peripheral myelin. Here, we used x-ray diffraction to examine time-dependent packing defects in unfixed myelin. At similar to 7 h post-dissection, WT and S63C(+/+) myelin showed native periods (175 angstrom) with the latter developing at most a few percent swollen myelin, whereas up to similar to 50% of S63C(+/-) (mutant P0 on heterozygous P0 null background) or P0(+/+) myelin swelled to periods of similar to 205 angstrom. In the same time frame, S63C(-/-) myelin was stable, remaining swollen at similar to 210 angstrom. Surprisingly, treatment of whole S63C(-/-) nerves with a reducing agent completely reverted swollen arrays to native spacing and also normalized the swollen arrays that had formed in S63C(+/-) myelin, the genotype most closely related to the human disorder. Western blot revealed P0-positive bands at similar to 27 and similar to 50 kDa, and MALDI-TOF mass spectrometry showed these bands consisted of Ser(34)-containing peptides or P0 dimers having oxidized Cys(34) residues. We propose that P0S34C forms ectopic disulfide bonds in trans between apposed Cys(34) side chains that retard wrapping during myelin formation causing hypomyelination. Moreover, the new bonds create a packing defect by stabilizing swollen membrane arrays that leads to demyelination.
Settore BIO/10 - Biochimica
Settore BIO/17 - Istologia
Settore BIO/13 - Biologia Applicata
Settore MED/26 - Neurologia
2010
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/953652
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