Literature DB >> 8593535

Substitution of alanine543 with a threonine residue at the carboxy terminal end of the beta-chain is associated with thermolabile hexosaminidase B in a Jewish family of Oriental ancestry.

R De Gasperi1, M A Gama Sosa, E E Grebner, D Mansfield, S Battistini, E L Sartorato, S S Raghavan, J G Davis, E H Kolodny.   

Abstract

Thermolabile forms of the lysosomal enzyme beta-hexosaminidase B (Hex B), likely to result from different genetic defects, have been described. Ten individuals in five generations of a family of Oriental Jewish ancestry were identified biochemically as carriers of a thermolabile Hex B form. The beta-chain thermolability was found to be associated with the presence of a G --> A transition at nucleotide 1627 of the HEX B gene causing the substitution of Ala543 with a threonine. Oriental Jew whose Hex B was heat labile. Since thermolabile Hex B has been shown to occur more frequently among Jews of Oriental origin, the Ala543 --> Thr mutation may be the common mutation associated with beta-chain thermolability in this ethnic group.

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Year:  1995        PMID: 8593535     DOI: 10.1006/bmme.1995.1053

Source DB:  PubMed          Journal:  Biochem Mol Med        ISSN: 1077-3150


  1 in total

1.  Molecular heterogeneity of late-onset forms of globoid-cell leukodystrophy.

Authors:  R De Gasperi; M A Gama Sosa; E L Sartorato; S Battistini; H MacFarlane; J F Gusella; W Krivit; E H Kolodny
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

  1 in total

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