Molecular and enzymatic analyses of lysosomal acid lipase in cholesteryl ester storage disease

Hong Du, Sulaiman Sheriff, Jorge Bezerra, Tatyana Leonova, Gregory A. Grabowski

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

Human lysosomal acid lipase (hLAL) is essential for the hydrolysis of cholesteryl esters and triglycerides in the lysosome. Defective hLAL activity leads to two autosomal recessive traits, Wolman disease (WD) or cholesteryl ester storage disease (CESD). Phenotypically, WD has accumulation of both triglycerides and cholesteryl esters, while CESD has mainly elevated cholesteryl esters. We characterized mutations in the hLAL gene from two CESD siblings. By reverse transcriptase-PCR (RT-PCR) and cDNA cloning and sequencing, we identified homozygous deletion mutations of nucleotides 863 to 934, in the hLAL transcript. Normal levels of LAL mRNA were detected. The deletion in mRNA is due to a G to A transition in the last nucleotide of exon 8 of the hLAL gene, a splice junction mutation (E8SJM) that resulted in exon skipping, and a predicted in-frame deletion of the 24 amino acids. [35S]Met metabolic labeling studies in fibroblasts showed a low level of E8SJM LAL (~38%) that was highly unstable. Heterologous expression of E8SJM LAL in insect cells gave an LAL with low catalytic activity toward cholesteryl oleate and triolein. The effects of this mutation are complex with the production of decreased amounts of an unstable LAL that is catalytically defective. The results suggest that E8SJM leads to essentially a null allele and that the differences in WD and CESD phenotype involve other factors.

Original languageEnglish (US)
Pages (from-to)126-134
Number of pages9
JournalMolecular Genetics and Metabolism
Volume64
Issue number2
DOIs
StatePublished - Jan 1 1998
Externally publishedYes

Fingerprint

Cholesterol Ester Storage Disease
Sterol Esterase
Cholesterol Esters
Wolman Disease
Mutation
Exons
Triglycerides
Nucleotides
Triolein
Messenger RNA
Sequence Deletion
Genes
Lysosomes
Reverse Transcriptase Polymerase Chain Reaction
Insects
Organism Cloning
Cloning
RNA-Directed DNA Polymerase
Hydrolysis
Complementary DNA

Keywords

  • Cholesterol ester storage disease
  • Immunoprecipitation
  • Lysosomal acid lipase
  • Wolman's disease

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Molecular Biology
  • Genetics
  • Endocrinology

Cite this

Molecular and enzymatic analyses of lysosomal acid lipase in cholesteryl ester storage disease. / Du, Hong; Sheriff, Sulaiman; Bezerra, Jorge; Leonova, Tatyana; Grabowski, Gregory A.

In: Molecular Genetics and Metabolism, Vol. 64, No. 2, 01.01.1998, p. 126-134.

Research output: Contribution to journalArticle

Du, Hong ; Sheriff, Sulaiman ; Bezerra, Jorge ; Leonova, Tatyana ; Grabowski, Gregory A. / Molecular and enzymatic analyses of lysosomal acid lipase in cholesteryl ester storage disease. In: Molecular Genetics and Metabolism. 1998 ; Vol. 64, No. 2. pp. 126-134.
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