THE ENZYMES, REGULATION, AND GENETICS OF BILE ACID SYNTHESIS

• Published in: Annual review of biochemistry 2003-01, Vol.72 (1), p.137-174
• Main Author: Russell, David W
• Format: Article
• Language: English
• Subjects: Acids; Animals; Bile; Bile Acids and Salts - biosynthesis; Bile Acids and Salts - chemistry; Bile Acids and Salts - genetics; Bile Acids and Salts - metabolism; catabolism; Cholesterol; Cholesterol - chemistry; Cholesterol - metabolism; Cholesterol - secretion; cytochrome P450; Enzymes; Enzymes - deficiency; Enzymes - genetics; Enzymes - metabolism; Essential nutrients; genetic disease; Genetics; Homeostasis; Humans; Liver - metabolism; Liver Diseases - enzymology; Liver Diseases - genetics; nuclear receptors; Receptors, Cytoplasmic and Nuclear - metabolism
• ISSN: 0066-4154; 1545-4509
• DOI: 10.1146/annurev.biochem.72.121801.161712

The synthesis and excretion of bile acids comprise the major pathway of cholesterol catabolism in mammals. Synthesis provides a direct means of converting cholesterol, which is both hydrophobic and insoluble, into a water-soluble and readily excreted molecule, the bile acid. The biosynthetic steps that accomplish this transformation also confer detergent properties to the bile acid, which are exploited by the body to facilitate the secretion of cholesterol from the liver. This role in the elimination of cholesterol is counterbalanced by the ability of bile acids to solubilize dietary cholesterol and essential nutrients and to promote their delivery to the liver. The synthesis of a full complement of bile acids requires 17 enzymes. The expression of selected enzymes in the pathway is tightly regulated by nuclear hormone receptors and other transcription factors, which ensure a constant supply of bile acids in an ever changing metabolic environment. Inherited mutations that impair bile acid synthesis cause a spectrum of human disease; this ranges from liver failure in early childhood to progressive neuropathy in adults.