Genetic homogeneity of Pelizaeus-Merzbacher disease

Tight linkage to the proteolipoprotein locus in 16 affected families

O. Boespflug-Tanguy, C. Mimault, J. Melki, A. Cavagna, G. Giraud, D. Pham Dinh, B. Dastugue, A. Dautigny, J. Aicardi, F. Gouttieres, N. Baumann, E. Bertini, A. David, A. Henocq, P. Landrieu, M. Tardieu, C. Leberre, B. Lemarec, G. Lyon, M. Mayer & 6 others J. M. Pinard, G. Ponsot, M. Mathieu, J. P. Saintive, R. Saura, L. Vallee

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Abstract

Among the numerous leukodystrophies that have an early onset and no biochemical markers, Pelizaeus-Merzbacher disease (PMD) is one that can be identified using strict clinical criteria and demonstrating an abnormal formation of myelin that is restricted to the CNS in electrophysiological studies and brain magnetic resonance imaging (MRI). In PMD, 12 different base substitutions and one total deletion of the genomic region containing the PLP gene have been reported, but, despite extensive analysis, PLP exon mutations have been found in only 10%-25% of the families analyzed. To test the genetic homogeneity of this disease, we have carried out linkage analysis with polymorphic markers of the PLP genomic region in 16 families selected on strict diagnostic criteria of PMD. We observed a tight linkage of the PMD locus with markers of the PLP gene (cDNA PLP, exon IV polymorphism) and of the Xq22 region (DXS17, DXS94, and DXS287), whereas the markers located more proximally (DXYS1X and DXS3) or distally (DXS11) were not linked to the PMD locus. Multipoint analysis gave a maximal location score for the PMD locus (13.98) and the PLP gene (8.32) in the same interval between DXS94 and DXS287, suggesting that in all families PMD is linked to the PLP locus. Mutations of the extraexonic PLP gene sequences or of another unknown close gene could be involved in PMD. In an attempt to identify molecular defects of this genomic region that are responsible for PMD, these results meant that RFLP analysis could be used to improve genetic counseling for the numerous affected families in which a PLP exon mutation could not be demonstrated.

Original languageEnglish
Pages (from-to)461-467
Number of pages7
JournalAmerican Journal of Human Genetics
Volume55
Issue number3
Publication statusPublished - 1994

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Pelizaeus-Merzbacher Disease
Exons
Genes
Mutation
Inborn Genetic Diseases
Genetic Counseling
Myelin Sheath
Restriction Fragment Length Polymorphisms
Complementary DNA
Biomarkers
Magnetic Resonance Imaging

ASJC Scopus subject areas

  • Genetics

Cite this

Boespflug-Tanguy, O., Mimault, C., Melki, J., Cavagna, A., Giraud, G., Pham Dinh, D., ... Vallee, L. (1994). Genetic homogeneity of Pelizaeus-Merzbacher disease: Tight linkage to the proteolipoprotein locus in 16 affected families. American Journal of Human Genetics, 55(3), 461-467.

Genetic homogeneity of Pelizaeus-Merzbacher disease : Tight linkage to the proteolipoprotein locus in 16 affected families. / Boespflug-Tanguy, O.; Mimault, C.; Melki, J.; Cavagna, A.; Giraud, G.; Pham Dinh, D.; Dastugue, B.; Dautigny, A.; Aicardi, J.; Gouttieres, F.; Baumann, N.; Bertini, E.; David, A.; Henocq, A.; Landrieu, P.; Tardieu, M.; Leberre, C.; Lemarec, B.; Lyon, G.; Mayer, M.; Pinard, J. M.; Ponsot, G.; Mathieu, M.; Saintive, J. P.; Saura, R.; Vallee, L.

In: American Journal of Human Genetics, Vol. 55, No. 3, 1994, p. 461-467.

Research output: Contribution to journalArticle

Boespflug-Tanguy, O, Mimault, C, Melki, J, Cavagna, A, Giraud, G, Pham Dinh, D, Dastugue, B, Dautigny, A, Aicardi, J, Gouttieres, F, Baumann, N, Bertini, E, David, A, Henocq, A, Landrieu, P, Tardieu, M, Leberre, C, Lemarec, B, Lyon, G, Mayer, M, Pinard, JM, Ponsot, G, Mathieu, M, Saintive, JP, Saura, R & Vallee, L 1994, 'Genetic homogeneity of Pelizaeus-Merzbacher disease: Tight linkage to the proteolipoprotein locus in 16 affected families', American Journal of Human Genetics, vol. 55, no. 3, pp. 461-467.
Boespflug-Tanguy, O. ; Mimault, C. ; Melki, J. ; Cavagna, A. ; Giraud, G. ; Pham Dinh, D. ; Dastugue, B. ; Dautigny, A. ; Aicardi, J. ; Gouttieres, F. ; Baumann, N. ; Bertini, E. ; David, A. ; Henocq, A. ; Landrieu, P. ; Tardieu, M. ; Leberre, C. ; Lemarec, B. ; Lyon, G. ; Mayer, M. ; Pinard, J. M. ; Ponsot, G. ; Mathieu, M. ; Saintive, J. P. ; Saura, R. ; Vallee, L. / Genetic homogeneity of Pelizaeus-Merzbacher disease : Tight linkage to the proteolipoprotein locus in 16 affected families. In: American Journal of Human Genetics. 1994 ; Vol. 55, No. 3. pp. 461-467.
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abstract = "Among the numerous leukodystrophies that have an early onset and no biochemical markers, Pelizaeus-Merzbacher disease (PMD) is one that can be identified using strict clinical criteria and demonstrating an abnormal formation of myelin that is restricted to the CNS in electrophysiological studies and brain magnetic resonance imaging (MRI). In PMD, 12 different base substitutions and one total deletion of the genomic region containing the PLP gene have been reported, but, despite extensive analysis, PLP exon mutations have been found in only 10{\%}-25{\%} of the families analyzed. To test the genetic homogeneity of this disease, we have carried out linkage analysis with polymorphic markers of the PLP genomic region in 16 families selected on strict diagnostic criteria of PMD. We observed a tight linkage of the PMD locus with markers of the PLP gene (cDNA PLP, exon IV polymorphism) and of the Xq22 region (DXS17, DXS94, and DXS287), whereas the markers located more proximally (DXYS1X and DXS3) or distally (DXS11) were not linked to the PMD locus. Multipoint analysis gave a maximal location score for the PMD locus (13.98) and the PLP gene (8.32) in the same interval between DXS94 and DXS287, suggesting that in all families PMD is linked to the PLP locus. Mutations of the extraexonic PLP gene sequences or of another unknown close gene could be involved in PMD. In an attempt to identify molecular defects of this genomic region that are responsible for PMD, these results meant that RFLP analysis could be used to improve genetic counseling for the numerous affected families in which a PLP exon mutation could not be demonstrated.",
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T1 - Genetic homogeneity of Pelizaeus-Merzbacher disease

T2 - Tight linkage to the proteolipoprotein locus in 16 affected families

AU - Boespflug-Tanguy, O.

AU - Mimault, C.

AU - Melki, J.

AU - Cavagna, A.

AU - Giraud, G.

AU - Pham Dinh, D.

AU - Dastugue, B.

AU - Dautigny, A.

AU - Aicardi, J.

AU - Gouttieres, F.

AU - Baumann, N.

AU - Bertini, E.

AU - David, A.

AU - Henocq, A.

AU - Landrieu, P.

AU - Tardieu, M.

AU - Leberre, C.

AU - Lemarec, B.

AU - Lyon, G.

AU - Mayer, M.

AU - Pinard, J. M.

AU - Ponsot, G.

AU - Mathieu, M.

AU - Saintive, J. P.

AU - Saura, R.

AU - Vallee, L.

PY - 1994

Y1 - 1994

N2 - Among the numerous leukodystrophies that have an early onset and no biochemical markers, Pelizaeus-Merzbacher disease (PMD) is one that can be identified using strict clinical criteria and demonstrating an abnormal formation of myelin that is restricted to the CNS in electrophysiological studies and brain magnetic resonance imaging (MRI). In PMD, 12 different base substitutions and one total deletion of the genomic region containing the PLP gene have been reported, but, despite extensive analysis, PLP exon mutations have been found in only 10%-25% of the families analyzed. To test the genetic homogeneity of this disease, we have carried out linkage analysis with polymorphic markers of the PLP genomic region in 16 families selected on strict diagnostic criteria of PMD. We observed a tight linkage of the PMD locus with markers of the PLP gene (cDNA PLP, exon IV polymorphism) and of the Xq22 region (DXS17, DXS94, and DXS287), whereas the markers located more proximally (DXYS1X and DXS3) or distally (DXS11) were not linked to the PMD locus. Multipoint analysis gave a maximal location score for the PMD locus (13.98) and the PLP gene (8.32) in the same interval between DXS94 and DXS287, suggesting that in all families PMD is linked to the PLP locus. Mutations of the extraexonic PLP gene sequences or of another unknown close gene could be involved in PMD. In an attempt to identify molecular defects of this genomic region that are responsible for PMD, these results meant that RFLP analysis could be used to improve genetic counseling for the numerous affected families in which a PLP exon mutation could not be demonstrated.

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