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Journal of Lipid Research, Vol. 45, 1608-1613, September 2004
Copyright © 2004 by American Society for Biochemistry and Molecular Biology




* Laboratories of Biochemical Genetics and Metabolism, The Rockefeller University, New York, NY
Metabolic Diseases, The Rockefeller University, New York, NY
** Molecular Genetics, The Rockefeller University, New York, NY
Department of Clinical Pharmacology, University of Bonn, Bonn, Germany
1 To whom correspondence should be addressed. e-mail: sehayee{at}rockefeller.edu
Screening of 932 adults on the Pacific island of Kosrae for plasma plant sterol levels disclosed three subjects, two of them asymptomatic, with phytosterolemia. Sequencing the ATP binding cassette subfamily G member 8 (ABCG8) gene revealed a novel exon 2 mutation that causes a change in codon 24 from glutamine to histidine and a frame shift followed by a premature stop codon, precluding the formation of a functional ABCG8 protein. Genotyping of 1,090 Kosraens revealed 150 as carriers, a 13.8% carrier rate. DNA sequencing of 67 carriers revealed the same mutation as in the probands. In carriers, plasma campesterol and sitosterol levels were 55% and 30% higher, respectively, than in noncarriers. Moreover, compared with noncarriers, carriers showed 21% lower plasma levels of lathosterol, a surrogate marker for cholesterol biosynthesis. There was no difference between the groups in plasma total cholesterol, triglycerides, apolipoprotein B, or apolipoprotein A-I levels.
In summary, on the island of Kosrae, a strong founder effect of a mutant ABCG8 allele results in a large number of carriers with increased plasma plant sterol levels and decreased lathosterol levels. The latter finding suggests that heterozygosity for a mutated ABCG8 allele results in a modest increase in dietary cholesterol absorption and a decrease in cholesterol biosynthesis.
Abbreviations: ABCG5 and ABCG8, ATP binding cassette subfamily G members 5 and 8
Supplementary key words ATP binding cassette subfamily G member 8 cholesterol absorption population genetics
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