Steroidogenic factor-1 (SF-1, NR5A1) and human disease

被引:120
作者
Ferraz-de-Souza, Bruno [1 ]
Lin, Lin [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; Adrenocortical tumor; Endometriosis; XY SEX REVERSAL; ADRENAL INSUFFICIENCY; CELL-PROLIFERATION; GLY146ALA POLYMORPHISM; ADRENOCORTICAL TUMORS; HETEROZYGOUS MUTATION; GONADAL-DYSGENESIS; NUCLEAR RECEPTOR; BINDING DOMAIN; 46; XY PATIENT;
D O I
10.1016/j.mce.2010.11.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Steroidogenic factor-1 (SF-1, Ad4BP, encoded by NR5A1) is a key regulator of adrenal and reproductive development and function. Based upon the features found in Nr5a1 null mice, initial attempts to identify SF-1 changes in humans focused on those rare individuals with primary adrenal failure, a 46,XY karyotype, complete gonadal dysgenesis and Mullerian structures. Although alterations affecting DNA-binding of SF-1 were found in two such cases, disruption of SF-1 is not commonly found in patients with adrenal failure. In contrast, it is emerging that variations in SF-1 can be found in association with a range of human reproductive phenotypes such as 46,XY disorders of sex development (DSD), hypospadias, anorchia, male factor infertility, or primary ovarian insufficiency in women. Overexpression or overactivity of SF-1 is also reported in some adrenal tumors or endometriosis. Therefore, the clinical spectrum of phenotypes associated with variations in SF-1 is expanding and the importance of this nuclear receptor in human endocrine disease is now firmly established. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:198 / 205
页数:8
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