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Galactosialidosis: molecular heterogeneity in biosynthesis and processing of protective protein for β-galactosidase

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Summary

Biosynthesis and processing of the protective protein for β-galactosidase in normal and galactosialidosis fibroblasts were investigated using specific antiserum preparations. A 45-kd precursor was processed to a mature 30-kd protein in normal fibroblasts. The mature protective protein was not detected in any of the twelve galactosialidosis fibroblast strains examined in this study. The precursor was not detected in two cases and in the others was of heterogeneous molecular weight, i.e., normal, abnormally low, or abnormally high. These molecular abnormalities were not correlated with clinical manifestations of the patients.

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References

  • D'Azzo A, Hoogeveen A, Reuser AJJ, Robinson D Galjaard H (1982) Molecular defect in combined β-galactosidase and neuraminidase in man. Proc Natl Acad Sci USA 79:4535–4539

    Google Scholar 

  • Goldberg MF, Cotlier E, Fichenscher LG, Kenyon K, Enat R, Borowsky SA (1971) Macular cherry-red spot, corneal clouding, and β-galactosidase deficiency. Clinical, biochemical and electron microscopic study of a new autosomal storage disease. Arch Intern Med 128:387–397

    Google Scholar 

  • Hasilik A, Neufeld EF (1980) Biosynthesis of lysosomal enzymes in fibroblasts. Synthesis as precursors of higher molecular weight. J Biol Chem 255:4937–4945

    Google Scholar 

  • Hoogeveen A, D'Azzo A, Brossmer R, Galjaard H (1981) Correction of combined β-galactosidase/neuraminidase deficiency in human fibroblasts. Biochem Biophys Res Commun 103:292–300

    Google Scholar 

  • Hoogeveen AT, Verheijen FW, Galjaard H (1983) The relation between human lysosomal β-galactosidase and its protective protein. J Biol Chem 258:12143–12146

    Google Scholar 

  • Kleijer WJ, Hoogeveen A, Verheijen FW, Niermeijer MF, Galjaard H, O'Brien JS, Warner TG (1979) Prenatal diagnosis of sialidosis with combined neuraminidase and β-galactosidase deficiency. Clin Genet 16:60–61

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structure protein during the assembly of the head of bacteriophage T4. Nature 227:680–685

    Google Scholar 

  • Motegi Y, Fujinaga T, Tamura H, Kuroume T, Omura K, Nanba E, Suzuki Y (1987) Severe infantile galactosialidosis: a case report. Nihon Shonika Gakkai Zasshi (Tokyo) 91:1459–1464

    Google Scholar 

  • Nanba E, Tsuji A, Omura K, Suzuki Y (1987a) Galactosialidosis: a direct evidence that a 46-kilodalton protein restores deficient enzyme activities in fibroblasts. Biochem Biophys Res Commun 144:138–142

    Google Scholar 

  • Nanba E, Tsuji A, Omura K, Suzuki Y (1987b) Galactosialidosis. Studies on residual enzymes in early and late onset clinical phenotypes. J Clin Biochem Nutr 3:149–157

    Google Scholar 

  • Nanba E, Tsuji A, Omura K, Suzuki Y (1988) GM1-gangliosidosis: abnormalities in biosynthesis and early processing of β-galactosidase in fibroblasts. Biochem Biophys Res Commun 152:794–880

    Google Scholar 

  • Palmeri S, Hoogeveen AT, Verheijen FW, Galjaard H (1986) Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes. Am J Hum Genet 38:137–148

    Google Scholar 

  • Proia RL, D'Azzo A, Neufeld EF (1984) Association of α-and β-subunits during the biosynthesis of β-hexosaminidase in cultured human fibroblasts. J Biol Chem 259:3350–3354

    Google Scholar 

  • Sakuraba H, Suzuki Y, Akagi M, Sakai M, Amano N (1983) β-Galactosidase-neuraminidase deficiency (galactosialidosis): clinical, pathological, and enzymatic studies in a postmortem case. Ann Neurol 13:497–503

    Google Scholar 

  • Suzuki Y, Nakamura N, Fukuoka K, Shimada Y, Uono M (1977) β-Galactosidase deficiency in juvenile and adult patients. Report of six Japanese cases and review of literature. Hum Genet 36:219–229

    Google Scholar 

  • Suzuki Y, Sakuraba H, Hayashi K, Suzuki K, Imahori K (1981) β-Galactosidase-neuraminidase deficiency: restoration of β-galactosidase activity by protease inhibitors. J Biochem 90:271–273

    Google Scholar 

  • Suzuki Y, Sakuraba H, Yamanaka T, Ko Y-M, Limori Y, Okamura Y, Hoogeveen AT (1985) Galactosialidosis: a comparative study of clinical and biochemical data on 22 patients. In: Arima M, Suzuki Y, Yabuuchi H (eds) The developing brain and its disorders. Karger, Basel, pp 161–175

    Google Scholar 

  • Takeda E, Kuroda Y, Tomita T, Kobayashi H, Ito M, Watanabe T, Toshima K, Hashimoto T, Miyao M (1984) Two siblings with β-galactosidase-neuraminidase deficiency (galactosialidosis) appearing in early childhood. No To Hattatsu 16:393–398

    Google Scholar 

  • Van Diggelen O, Hoogeveen AT, Smith PJ, Reuser AJJ, Galjaard H (1982) Enhanced proteolytic degradation of normal β-galactosidase in the lysosomal storage disease with combined β-galactosidase and neuraminidase deficiency. Biochim Biophys Acta 703: 69–76

    Google Scholar 

  • Verheijen FW, Palmeri S, Hoogeveen AT, Galjaard H (1985) Human placental neuraminidase. Activation, stabilization and association with β-galactosidase and its ‘protective’ protein. Eur J Biochem 149:315–321

    Google Scholar 

  • Wenger D, Tarby TJ, Wharton C (1978) Macular cherry-red spots and myoclonus with dementia: coexistent neuraminidase and β-galactosidase deficiencies. Biochem Biophys Res Commun 82:589–595

    Google Scholar 

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Nanba, E., Tsuji, A., Omura, K. et al. Galactosialidosis: molecular heterogeneity in biosynthesis and processing of protective protein for β-galactosidase. Hum Genet 80, 329–332 (1988). https://doi.org/10.1007/BF00273645

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  • DOI: https://doi.org/10.1007/BF00273645

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