A novel mutation in the HEXA gene specific to Tay-Sachs disease carriers of Jewish Iraqi origin

Clin Genet. 2000 May;57(5):398-400. doi: 10.1034/j.1399-0004.2000.570512.x.

Abstract

An increased frequency of carriers of 1:140, as defined by reduced hexosaminidase A (HexA) activity, was observed among Iraqi Jews participating in the Tay-Sachs disease (TSD) carrier detection program. Prior to this finding, TSD among Jews had been restricted to those of Eastern European (Ashkenazi) and Moroccan descent with carrier frequencies of 1:29 and 1:110 for Jews of Ashkenazi and Moroccan extraction, respectively. A general, pan-ethnic frequency of approximately 1:280 has been observed among other Jewish Israeli populations. Analysis of 48 DNA samples from Iraqi Jews suspected, by enzymatic assay, to be carriers revealed a total of five mutations, one of which was novel. In nine carriers (19%), a known mutation typical to either Ashkenazi or Moroccan Jews was identified. DeltaF304/ 305 was detected in four individuals, and + 1278TATC in three. G269S and R170Q each appeared in a single person. The new mutation, G749T, resulting in a substitution of glycine to valine at position 250 has been found in 19 of the DNA samples (40%). This mutation was not detected among 100 non-carrier, Iraqi Jews and 65 Ashkenazi enzymatically determined carriers. Aside from Ashkenazi and Moroccan Jews, a specific mutation in the HEXA gene has now also been identified in Jews of Iraqi descent.

Publication types

  • Comparative Study

MeSH terms

  • Amino Acid Substitution
  • DNA / analysis
  • DNA / blood
  • DNA Primers
  • Humans
  • Iraq / ethnology
  • Jews / genetics*
  • Mutation*
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Tay-Sachs Disease / ethnology
  • Tay-Sachs Disease / genetics*
  • beta-Hexosaminidase alpha Chain / genetics*

Substances

  • DNA Primers
  • DNA
  • HEXA protein, human
  • beta-Hexosaminidase alpha Chain