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J Biol Chem, Vol. 274, Issue 43, 30843-30848, October 22, 1999
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From the Squalene synthase (SS) catalyzes the reductive
head-to-head condensation of two molecules of farnesyl diphosphate to
form squalene, the first specific intermediate in the cholesterol
biosynthetic pathway. We used gene targeting to knock out the mouse SS
gene. The mice heterozygous for the mutation (SS+/
Department of Metabolic Diseases, the
Department of Cardiology, and the ¶ Department of
Pathology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo,
Bunkyo-ku, Tokyo 113-8655, Japan
) were
apparently normal. SS+/
mice showed 60% reduction in the
hepatic mRNA levels of SS compared with SS+/+ mice.
Consistently, the SS enzymatic activities were reduced by 50% in the
liver and testis. Nevertheless, the hepatic cholesterol synthesis was
not different between SS+/
and SS+/+ mice,
and plasma lipoprotein profiles were not different irrespective of the
presence of the low density lipoprotein receptor, indicating that SS is
not a rate-limiting enzyme in the cholesterol biosynthetic pathway. The
mice homozygous for the disrupted SS gene (SS
/
) were
embryonic lethal around midgestation. E9.5-10.5 SS
/
embryos exhibited severe growth retardation and defective neural tube
closure. The lethal phenotype was not rescued by supplementing the dams
either with dietary squalene or cholesterol. We speculate that
cholesterol is required for the development, particularly of the
nervous system, and that the chorioallantoic circulatory system is not
mature enough to supply the rapidly growing embryos with maternal
cholesterol at this developmental stage.
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