Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease

J Lipid Res. 2000 Jan;41(1):23-31.

Abstract

Cholesteryl ester storage disease and Wolman disease are rare autosomal recessive lipoprotein-processing disorders caused by mutations in the gene encoding human lysosomal acid lipase. Thus far we have elucidated the genetic defects in 15 unrelated CESD patients. Seven were homozygotes for the prevalent hLAL exon 8 splice junction mutation which results in incomplete exon skipping, while eight probands were compound heterozygotes for E8SJM and a rare mutation on the second chromosome. In this report, we describe the molecular basis of CESD in three compound heterozygous subjects of Czech and Irish origin. RFLP and DNA sequence analysis revealed that they were heteroallelic for the common G(934)-->A substitution in exon 8 of the hLAL gene and a mutation which, if inherited on both alleles, would be expected to result in complete loss of enzyme activity and to cause Wolman disease. In patients A. M. and J. J., two nucleotide deletions in exons 7 and 10 were detected, involving a T at position 722, 723, or 724 and a G in a stretch of five guanosines at positions 1064;-1068 of the hLAL cDNA. Both mutations result in premature termination of protein translation at residues 219 and 336, respectively, and in the production of truncated, inactive enzymes. Subject D. H., in contrast, is a compound heterozygote for the Arg(44)-->Stop mutation previously described in a French CESD proband. Combined with data in the literature, our results demonstrate that compound heterozygosity for a mutation causing Wolman disease is common among cholesteryl ester storage disease patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Child
  • Child, Preschool
  • Cholesterol Ester Storage Disease / genetics*
  • Cholesterol Ester Storage Disease / pathology
  • DNA Primers
  • Exons
  • Female
  • Hepatomegaly
  • Heterozygote*
  • Humans
  • Hyperlipoproteinemias / pathology
  • Male
  • Mutation*
  • Polymorphism, Restriction Fragment Length
  • Recombinant Fusion Proteins / genetics
  • Splenomegaly
  • Wolman Disease / genetics*
  • Wolman Disease / pathology

Substances

  • DNA Primers
  • Recombinant Fusion Proteins