Natural Mutagenesis Study of the Human Steroid 5α-Reductase 2 Isozyme

W. Christian Wigley, James S. Prihoda, I. Mowszowicz, Berenice B. Mendonca, Maria I. New, Jean D. Wilson, David W. Russell

Research output: Contribution to journalArticlepeer-review

136 Scopus citations

Abstract

The enzyme steroid 5α-reductase utilizes NADPH to reduce the double bonds of a variety of steroid substrates with generalized 3-oxo, Δ4,5 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 5α-reductase isozymes, designated types 1 and 2, which have different biochemical and pharmacological properties. Inherited deficiencies of 5α-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 5α-reductase 2 gene in subjects with 5α-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 5α-reductase type 2 isozyme.

Original languageEnglish (US)
Pages (from-to)1265-1270
Number of pages6
JournalBiochemistry
Volume33
Issue number5
DOIs
StatePublished - Feb 1 1994

ASJC Scopus subject areas

  • Biochemistry

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