Regional mapping of human genes for hexosaminidase B and diphtheria toxin sensitivity on chromosome 5 using mouse × human hybrid cells
- 1 November 1977
- journal article
- Published by Springer Nature in Somatic Cell and Molecular Genetics
- Vol. 3 (6) , 629-638
- https://doi.org/10.1007/bf01539070
Abstract
Mouse 3T3 (TK−) cells were fused to human leukocytes containing a balanced translocation [ins(3;5) (q27;q13q15)] in which part of the long arm of a chromosome 5 has been inserted into the long arm of a chromosome 3. Two independent, primary hybrid clones (XVI-10C; XVI-18A) retained the deleted chromosome 5 [del(5) (q13q15)] translocation product and were informative for regional mapping on chromosome 5 of genes involved in expression of hexosaminidase B (HEX B ) and diphtheria toxin sensitivity (DTS). Both XVI-10C and XVI-18A clones were sensitive to diphtheria toxin. Toxin-resistant derivatives of these clones (XVI-10C DTR; XVI-18A DTR) were analyzed for chromosome content and expression of Hex B activity, as were XVI-10C and XVI-18A cells which had not been exposed to diphtheria toxin. The results of this study provide evidence for localization ofDTS to region 5q15→5qter on the long arm of chromosome 5, and localization ofHEX B to region 5pter→5q13.Keywords
This publication has 18 references indexed in Scilit:
- Subunit structure of human hexosaminidase verified: interconvertibility of hexosaminidase isozymesNature, 1975
- Assignment of the human gene for hexosaminidase B to chromosome 5Experimental Cell Research, 1975
- A study of hexosaminidases in interspecific hybrids and in GM2 gangliosidosis with a discussion on their genetic controlAnnals of Human Genetics, 1975
- Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13Annals of Human Genetics, 1975
- Hexosaminidase-A and Hexosamini-dase-B: Studies in Tay-Sachs' and Sandhoff's DiseaseNature, 1973
- TAY-SACHS DISEASE: INTERRELATION OF HEXOSAMINIDASES A AND BThe Lancet, 1972
- Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase ComponentScience, 1969
- Somatic Cell Hybrid between the Established Human Line D98 (Presumptive HeLa) and 3T3Science, 1969
- Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organsLife Sciences, 1968
- Selection of Hybrids from Matings of Fibroblasts in vitro and Their Presumed RecombinantsScience, 1964