The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders

Молекулярная биология, биохимия и физиология стероидогенеза у человека и его нарушений
Walter L. Miller, Richard J. Auchus
2011-02-01

CYP11A1 (P450scc)disorders of steroidogenesishuman steroidogenesishydroxysteroid dehydrogenasessteroidogenic enzymes
Steroidogenesis entails processes by which cholesterol is converted to biologically active steroid hormones. Whereas most endocrine texts discuss adrenal, ovarian, testicular, placental, and other steroidogenic processes in a gland-specific fashion, steroidogenesis is better understood as a single process that is repeated in each gland with cell-type-specific variations on a single theme. Thus, understanding steroidogenesis is rooted in an understanding of the biochemistry of the various steroidogenic enzymes and cofactors and the genes that encode them. The first and rate-limiting step in steroidogenesis is the conversion of cholesterol to pregnenolone by a single enzyme, P450scc (CYP11A1), but this enzymatically complex step is subject to multiple regulatory mechanisms, yielding finely tuned quantitative regulation. Qualitative regulation determining the type of steroid to be produced is mediated by many enzymes and cofactors. Steroidogenic enzymes fall into two groups: cytochrome P450 enzymes and hydroxysteroid dehydrogenases. A cytochrome P450 may be either type 1 (in mitochondria) or type 2 (in endoplasmic reticulum), and a hydroxysteroid dehydrogenase may belong to either the aldo-keto reductase or short-chain dehydrogenase/reductase families. The activities of these enzymes are modulated by posttranslational modifications and by cofactors, especially electron-donating redox partners. The elucidation of the precise roles of these various enzymes and cofactors has been greatly facilitated by identifying the genetic bases of rare disorders of steroidogenesis. Some enzymes not principally involved in steroidogenesis may also catalyze extraglandular steroidogenesis, modulating the phenotype expected to result from some mutations. Understanding steroidogenesis is of fundamental importance to understanding disorders of sexual differentiation, reproduction, fertility, hypertension, obesity, and physiological homeostasis.
1
Conversion of cholesterol to pregnenolone by mitochondrial P450scc (CYP11A1) is the first and rate-limiting step, controlled by multiple regulatory mechanisms.
2
Genetic studies of rare steroidogenesis disorders have clarified enzyme and cofactor functions, while extraglandular enzymes can modify mutation-associated phenotypes.
3
Steroid output specificity is determined by coordinated actions of cytochrome P450 enzymes, hydroxysteroid dehydrogenases, cofactors, and electron-donating redox partners.
4
Steroidogenesis is best understood as one conserved cholesterol-to-steroid process repeated across glands, with cell-type-specific enzymatic variations.
5
Steroidogenesis is central to understanding disorders of sexual differentiation, reproduction, fertility, hypertension, obesity, and physiological homeostasis.
6
Steroidogenic enzyme activities are modulated by subcellular localization, enzyme families, posttranslational modifications, and redox cofactors.

Human steroidogenesis across steroidogenic tissues and cells, including its associated enzymes, cofactors, and genetic disorders

The molecular, biochemical, physiological, and regulatory mechanisms of steroidogenesis and how their disruption causes steroidogenesis disorders

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2011-02-01
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Walter L. Miller
Richard J. Auchus
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