Natural mutagenesis study of the human steroid 5α-reductase 2 isozyme

• Published in: Biochemistry (Easton) Vol. 33; no. 5; pp. 1265 - 1270
• Main Authors: WIGLEY, W. C, PRIHODA, J. S, MOWSZOWICZ, I, MENDONCA, B. B, NEW, M. I, WILSON, J. D, RUSSELL, D. W
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 08.02.1994
• Subjects: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - deficiency; 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - genetics; Base Sequence; Biological and medical sciences; Classical genetics, quantitative genetics, hybrids; DNA; Female; Fundamental and applied biological sciences. Psychology; Genetics of eukaryotes. Biological and molecular evolution; Human; Humans; Isoenzymes - genetics; Male; Molecular Sequence Data; Mutagenesis; Human; NADPH; Enzyme; Isozyme; Deficiency; Molecular interaction; Cofactor; Structure function relationship; Substrate; Enzymatic activity; Gene; Oxidoreductases; Mutation
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00171a029

The enzyme steroid 5 alpha-reductase utilizes NADPH to reduce the double bonds of a variety of steroid substrates with generalized 3-oxo, delta 4,5 structures. One substrate for this membrane-bound enzyme is testosterone, whose reduction to dihydrotestosterone is required for the embryonic differentiation of the external male genitalia and prostate. There are two 5 alpha-reductase isozymes, designated types 1 and 2, which have different biochemical and pharmacological properties. Inherited deficiencies of 5 alpha-reductase type 2 result in a form of male pseudohermaphroditism in which the external genitalia fail to develop normally. Here, nine additional mutations in the 5 alpha-reductase 2 gene in subjects with 5 alpha-reductase deficiency are described. The biochemical consequences of these mutations, as well as 13 previously identified missense mutations, were characterized by recreating the mutations in an expressible cDNA and transfecting into mammalian cells. Twelve of the 22 mutations inactivated the enzyme. The remaining 10 mutations impaired enzyme function by affecting either substrate or cofactor binding. Almost all mutations decreased the half-life of the protein, and all but one of the impaired enzymes had an altered pH optimum. The mutations provide insight into functional domains in the protein as well as an unusual acidic pH optimum characteristic of the 5 alpha-reductase type 2 isozyme.