Schimmer Bernard P, White Perrin C
Banting and Best Department of Medical Research, University of Toronto, Toronto, Ontario M5G1L6, Canada.
Mol Endocrinol. 2010 Jul;24(7):1322-37. doi: 10.1210/me.2009-0519. Epub 2010 Mar 4.
The orphan nuclear receptor steroidogenic factor 1 (SF-1, also called Ad4BP, encoded by the NR5A1 gene) is an essential regulator of endocrine development and function. Initially identified as a tissue-specific transcriptional regulator of cytochrome P450 steroid hydroxylases, studies of both global and tissue-specific knockout mice have demonstrated that SF-1 is required for the development of the adrenal glands, gonads, and ventromedial hypothalamus and for the proper functioning of pituitary gonadotropes. Many genes are transcriptionally regulated by SF-1, and many proteins, in turn, interact with SF-1 and modulate its activity. Whereas mice with heterozygous mutations that disrupt SF-1 function have only subtle abnormalities, humans with heterozygous SF-1 mutations can present with XY sex reversal (i.e. testicular failure), ovarian failure, and occasionally adrenal insufficiency; dysregulation of SF-1 has been linked to diseases such as endometriosis and adrenocortical carcinoma. The current state of knowledge of this important transcription factor will be reviewed with a particular emphasis on the pioneering work on SF-1 by the late Keith Parker.
孤儿核受体类固醇生成因子1(SF-1,也称为Ad4BP,由NR5A1基因编码)是内分泌发育和功能的重要调节因子。最初被鉴定为细胞色素P450类固醇羟化酶的组织特异性转录调节因子,对全身性和组织特异性基因敲除小鼠的研究表明,SF-1是肾上腺、性腺和下丘脑腹内侧发育以及垂体促性腺细胞正常功能所必需的。许多基因受SF-1转录调控,反过来,许多蛋白质与SF-1相互作用并调节其活性。虽然具有破坏SF-1功能的杂合突变的小鼠仅有轻微异常,但具有SF-1杂合突变的人类可能出现XY性反转(即睾丸功能衰竭)、卵巢功能衰竭,偶尔还会出现肾上腺功能不全;SF-1失调与子宫内膜异位症和肾上腺皮质癌等疾病有关。本文将综述这一重要转录因子的当前知识状态,特别强调已故基思·帕克关于SF-1的开创性工作。