Steroidogenic Factor-1 and Human Disease

被引:54
作者
El-Khairi, Ranna [1 ]
Achermann, John C. [1 ]
机构
[1] UCL, UCL Inst Child Hlth, Clin & Mol Genet Unit, Dev Endocrinol Res Grp, London WC1N 1EH, England
基金
英国惠康基金;
关键词
steroidogenic factor-1 (SF-1); NR5A1; adrenal failure; 46; XY disorders of sex development (DSD); primary ovarian insufficiency (POI); infertility; XY SEX REVERSAL; ADRENAL DEVELOPMENT; HETEROZYGOUS MUTATION; GONADAL-DYSGENESIS; CELL-PROLIFERATION; NUCLEAR RECEPTOR; BINDING DOMAIN; 46; XY SUBJECTS; NR5A1; GENE;
D O I
10.1055/s-0032-1324720
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Steroidogenic factor-1 (SF-1) (Ad4BP, NR5A1) is a nuclear receptor that plays a key role in adrenal and reproductive development and function. Deletion of the gene encoding Sf-1 (Nr5a1) in mice results in severe developmental defects of the adrenal gland and gonad. Consequently, initial work on the potential effects of SF-1 disruption in humans focused on individuals with primary adrenal failure, a 46,XY karyotype, complete gonadal dysgenesis, and Mullerian structures. This is a rare phenotype, but has been reported on two occasions, because of alterations that affect key DNA-binding domains of SF-1. Attention then turned to a potential wider role of SF-1 in human adrenal and reproductive disorders. Although changes in SF-1 only very rarely cause isolated adrenal failure, it is emerging that variations in SF-1 are a surprisingly frequent cause of reproductive dysfunction in humans. In 46,XY disorders of sex development, a spectrum of phenotypes has been reported including severe and partial forms of gonadal (testicular) dysgenesis, hypospadias, anorchia with microphallus, and even male factor infertility. In 46,XX females, alterations in 5F-1 are associated with primary ovarian insufficiency. Thus, SF-1 seems be a more significant factor in human reproductive health than was first envisioned, with implications for adults as well as children.
引用
收藏
页码:374 / 381
页数:8
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