Skip to main content
Log in

Genetic linkage studies of the human glycosphingolipid β-galactosidases

  • Published:
Biochemical Genetics Aims and scope Submit manuscript

Abstract

The genetic linkage relationships of the human glycosphingolipid β-galactosidases were determined using human-mouse somatic cell hybrids. A new method was devised for the estimation of human galactosylceramide, lactosylceramide, and GMI-ganglioside β-galactosidase activities in the presence of their mouse counterparts, which takes advantage of the reproducible specific activity of lysosomal hydrolases under a given set of culture conditions and is based on differences in both pH optima and sensitivity to chloride ion. Human and mouse chromosomes were identified by their characteristic banding patterns obtained after quinacrine staining, and the optimum glycolipid β-galactosidase activity was determined for three different substrates. A ratio was defined for each activity which was the specific activity at the human pH optimum divided by the specific activity at the mouse pH optimum. Linear regression analysis was used to test for concordant segregation between pH ratios for each enzyme and the frequency of occurrence of different human chromosomes in the man-mouse somatic hybrid clones. The results obtained from two independent series of hybrid clones indicated that human β-galactosidase activities consistently segregated with human chromosome 12 in these somatic cell hybrids.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Boone, C., Chen, T.-R., and Ruddle, F. H. (1972). Assignment of three human genes to chromosomes (LDH-A to 11, TK to 17 and IDH to 20) and evidence for translocation between human and mouse chromosomes in somatic cell hybrids. Proc. Natl. Acad. Sci. 69510.

    Google Scholar 

  • Bootsma, D. (1976). Genetic complementation, gene mapping, and gene transfer in somatic cell hybrids. In Abstracts Fifth International Congress of Human Genetics, p. 3.

  • Callahan, J. W., and Gerrie, J. (1976). GM1-ganglioside and lactosylceramide β-galactosidase from rabbit brain: Inhibitor and substrate competition studies. Can. J. Biochem. 54803.

    Google Scholar 

  • Case, M. E., and Giles, N. H. (1975). Genetic evidence on the organization and action of the ga-1 gene product: A protein regulating the induction of three enzymes in quinate catabolism in Neurospora crassa. Proc. Natl. Acad. Sci. 72553.

    Google Scholar 

  • Chen, T.-R., McMorris, F. A., Creagan, R., Ricciuti, F., Tischfield, J., and Ruddle, F. H. (1973). Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man. Am. J. Hum. Genet. 25200.

    Google Scholar 

  • Demerec, M. (1965). Homology and divergence in genetic material of Salmonella typhimurium and Escherichia coli. In Bryson, V., and Vogel, H. J. (eds.), Evolving Genes and Proteins, Academic Press, New York, pp. 505–510.

    Google Scholar 

  • Farber, R. A. (1973). Gene dosage and the expression of electrophoretic patterns in heteroploid mouse cell lines. Genetics 74521.

    Google Scholar 

  • Hers, H. G., and van Hoof, F. (1973) Lysosomes and Storage Diseases, Academic Press, New York.

    Google Scholar 

  • Lalley, P. A., Rattazzi, M. C., and Shows, T. B. (1974). Human β-D-N-acetylhexosaminidase A and B: Expression and linkage relationships in somatic cell hybrids. Proc. Natl. Acad. Sci. 711569.

    Google Scholar 

  • Lucchesi, J. C., and Rawls, J. M. (1973). Regulations of gene function: A comparison of enzyme activity levels in relation to gene dosage in diploids and triploids of Drosophila melanogaster. Biochem. Genet. 941.

    Google Scholar 

  • Metzenberg, R. L. (1972). Genetic regulatory systems in Neurospora. Ann. Rev. Genet. 6111.

    Google Scholar 

  • Miller, A. L., Frost, R. G., and O'Brien, J. S. (1976). Purification of human liver acid β-D-galactosidases using affinity chromatography. Anal. Biochem. 74537.

    Google Scholar 

  • Nishimura, K., and Amano, R. (1976). Partial purification and properties of porcine thymus lactosylceramide β-galactosidase. J. Biochem. 80209.

    Google Scholar 

  • Norden, A. G. W., and O'Brien, J. S. (1975). An electrophoretic variant of β-galactosidase with altered catalytic properties in a patient with GM1-gangliosidosis. Proc. Natl. Acad. Sci. 72240.

    Google Scholar 

  • Priest, R. E., and Priest, J. H. (1969). Diploid and tetraploid clonal cells in culture: Gene ploidy and synthesis of collagen. Biochem. Genet. 3371.

    Google Scholar 

  • Ruddle, F. H., and Creagan, R. P. (1975). Parasexual approaches to the genetics of man. Ann. Rev. Genet. 9407.

    Google Scholar 

  • Rushton, A. R. (1975). The biochemical genetics of the human glycosphingolipid β-galactosidases. Ph.D. dissertation, University of Chicago.

  • Rushton, A. R. (1976). Quantitative analysis of human chromosome segregation in man-mouse somatic cell hybrids. Cytogenet. Cell Genet. 71854.

    Google Scholar 

  • Rushton, A. R., and Dawson, G. (1975). Glycosphingolipid β-galactosidases of cultured mammalian cells. Characterization of the enzymes from mouse cell line LMTK — and human Lesch-Nyhan fibroblasts. Biochim. Biophys. Acta 38892.

    Google Scholar 

  • Schollen, J., Bender, K., and van Deimling, O. (1975). Esterase. XXI. ES-9, a possibly new polymorphic esterase in Mus musculus genetically linked to Es-2. Biochem. Genet. 13369.

    Google Scholar 

  • Shows, T. B. (1972). Genetics of human-mouse somatic cell hybrids: Linkage of human genes for lactate dehydrogenase-A and esterase-A4. Proc. Natl. Acad. Sci. 69348.

    Google Scholar 

  • Snedecor, G. W., and Cochran, W. G. (1967). Statistical Methods, Iowa State University Press, Ames, Ia.

    Google Scholar 

  • Tanaka, H., and Suzuki, K. (1975). Lactosylceramide β-galactosidase in human sphingolipidoses: Evidence for two genetically distinct enzymes. J. Biol. Chem. 2502324.

    Google Scholar 

  • Tanaka, H., and Suzuki, K. (1976). Specificities of the two genetically distinct β-galactosidases in human sphingolipodoses. Arch. Biochem. Biophys. 175332.

    Google Scholar 

  • Wenger, D. A., Sattler, M., and Hiatt, W. (1974). Globoid cell leukodystrophy: Deficiency of lactosyl ceramide β-galactosidase. Proc. Natl. Acad. Sci. 71854.

    Google Scholar 

  • Wenger, D. A., Sattler, M., Clark, C., Tanaka, H., Suzuki, K., and Dawson, G. (1975). Lactosyl ceramidosis Normal activity for two lactosyl ceramide β-galactosidases. Science 1881310.

    Google Scholar 

  • Westerveld, A., Visser, R. P. L. S., Freeke, M. A., and Bootsma, D. (1972). Evidence for linkage of 3-phosphoglycerate kinase, hypoxanthine-guanine-phosphoribosyl transferase and glucose 6-phosphate dehydrogenase loci in Chinese hamster cells studied by using a relationship between gene multiplicity and enzyme activity. Biochem. Genet. 733.

    Google Scholar 

  • Womack, J. E. (1975). Esterase-6 (Es-6) in laboratory mice: Hormone-influenced expression and linkage relationship to oligosyndactylism (Os), esterase-1 (Es-1), and esterase-2 (Es-2) in chromosome 8. Biochem. Genet. 13311.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This investigation was supported by USPHS Research Grants HD-06426 and HD-04583 and National Foundation March of Dimes Grant I-340. A. R. R. was supported by PHS Training Grant No. 2 T05 GMO 1939 from the NIGMS. G. D. is a Joseph P. Kennedy, Jr., Scholar, and the recipient of Research Career Development Award NS-00029.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rushton, A.R., Dawson, G. Genetic linkage studies of the human glycosphingolipid β-galactosidases. Biochem Genet 15, 1071–1082 (1977). https://doi.org/10.1007/BF00484498

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00484498

Key words

Navigation