UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

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

Ferraz-de-Souza, B; Lin, L; Achermann, JC; (2011) Steroidogenic factor-1 (SF-1, NR5A1) and human disease. MOLECULAR AND CELLULAR ENDOCRINOLOGY , 336 (1-2) 198 - 205. 10.1016/j.mce.2010.11.006. Gold open access

Warning

A more recent version of this eprint is available. Click here to view it.

Abstract

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.

Type: Article
Title: Steroidogenic factor-1 (SF-1, NR5A1) and human disease
Location: San Diego, CA
Open access status: An open access publication
DOI: 10.1016/j.mce.2010.11.006
Keywords: 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
UCL classification: UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
URI: https://discovery.ucl.ac.uk/id/eprint/467910

Available Versions of this Item

Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item