Literature DB >> 113895

GM1-gangliosidosis: chromosome 3 assignment of the beta-galactosidase-A gene (beta GALA).

T B Shows, L R Scrafford-Wolff, J A Brown, M H Meisler.   

Abstract

The structural gene (beta GALA) coding for lysosomal beta-galactosidase-A (EC 3.2.1.23) has been assigned to human chromosome 3 using man--mouse somatic cell hybrids. Human beta-galactosidase-A was identified in cell hybrids with a species-specific antiserum to human liver beta-galactosidase-A. The antiserum precipitates beta-galactosidase-A from human tissues, cultured cells, and cell hybrids, and recognizes cross-reacting material from a patient with GM1 gangliosidosis. We have analyzed 90 primary man--mouse hybrids derived from 12 separate fusion experiments utilizing cells from 9 individuals. Enzyme segregation analysis excluded all chromosomes for beta GALA assignment except chromosome 3. Concordant segregation of chromosomes and enzymes in 16 cell hybrids demonstrated assignment of beta GALA to chromosome 3; all other chromosomes were excluded. The evidence suggests that GM1 gangliosidosis is a consequence of mutation at this beta GALA locus on chromosome 3.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 113895     DOI: 10.1007/bf01539157

Source DB:  PubMed          Journal:  Somatic Cell Genet        ISSN: 0098-0366


  15 in total

1.  Native SDS-PAGE: high resolution electrophoretic separation of proteins with retention of native properties including bound metal ions.

Authors:  Andrew B Nowakowski; William J Wobig; David H Petering
Journal:  Metallomics       Date:  2014-05       Impact factor: 4.526

2.  The mouse gene (Mobp) encoding myelin-associated oligodendrocytic basic protein maps to distal chromosome 9.

Authors:  A S McCallion; J L Guénet; P Montague; I R Griffiths; A Savioz; R W Davies
Journal:  Mamm Genome       Date:  1996-11       Impact factor: 2.957

3.  Chromosomal assignment of the gene for the human beta 2-adrenergic receptor.

Authors:  J R Sheppard; J M Wehner; J D McSwigan; T B Shows
Journal:  Proc Natl Acad Sci U S A       Date:  1983-01       Impact factor: 11.205

4.  The genetic defect in the various types of human beta-galactosidase deficiency.

Authors:  H L Hoeksema; J De Wit; A Westerveld
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

5.  Lysosomal arylsulfatase deficiencies in humans: chromosome assignments for arylsulfatase A and B.

Authors:  C DeLuca; J A Brown; T B Shows
Journal:  Proc Natl Acad Sci U S A       Date:  1979-04       Impact factor: 11.205

6.  The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation.

Authors:  P L Chang; O T Mueller; R M Lafrenie; P A Varey; N E Rosa; R G Davidson; W M Henry; T B Shows
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

7.  Regional assignment of the structural gene for human alpha-L-iduronidase.

Authors:  E H Schuchman; K H Astrin; P Aula; R J Desnick
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

8.  Leukocyte and fibroblast interferon genes are located on human chromosome 9.

Authors:  D Owerbach; W J Rutter; T B Shows; P Gray; D V Goeddel; R M Lawn
Journal:  Proc Natl Acad Sci U S A       Date:  1981-05       Impact factor: 11.205

9.  The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3.

Authors:  E Baker; X H Guo; A M Orsborn; G R Sutherland; D F Callen; J J Hopwood; C P Morris
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

10.  Assignment of the glyoxalase II gene (HAGH) to human chromosome 16.

Authors:  N K Honey; T B Shows
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.