Wang Z N, Bassett M, Rainey W E
Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology, The University of Texas, Southwestern Medical Center at Dallas, Dallas, Texas 75390, USA.
J Mol Endocrinol. 2001 Oct;27(2):255-8. doi: 10.1677/jme.0.0270255.
Liver receptor homologue-1 (LRH-1, designated NR5A2) is a mammalian homologue of Drosophila fushi tarazu factor (dFTZ-F1) and structurally belongs to the orphan nuclear receptor superfamily. LRH-1 can recognize the DNA sequence 5'-AAGGTCA-3', the canonical recognition motif for steroidogenic factor 1 (SF-1). Herein, we hypothesized that LRH-1 might play a role in the regulation of human adrenal expression of steroidogenic enzymes. To test this hypothesis, LRH-1 expression in human adult and fetal adrenal glands was examined by RT-PCR analysis. The fetal and adult adrenal glands, as well as liver and pancreas, were observed to express LRH-1 mRNA using RT-PCR. The ability of LRH-1 to enhance transcription of the gene encoding human 11 beta- hydroxylase (hCYP11B1) was then examined using the H295R adrenal cell line. LRH-1 co-transfection with hCYP11B1 luciferase promoter constructs caused a 25-fold induction of luciferase activity. Furthermore, co-transfection of a hCYP11B1 reporter construct containing a mutation in the SF-1 binding cis-element abolished the stimulatory effect of both SF-1 and LRH-1. Electrophoretic mobility shift assay (EMSA) demonstrated that LRH-1 could bind to the SF-1 response element. Taken together, our data suggested that LRH-1 is expressed in the adrenal, and can substitute for SF-1 to enhance transcription of genes encoding certain of the steroid-metabolizing enzymes. A role for LRH-1 in the regulation of adrenal or gonadal steroid hormone production should be further studied.
肝脏受体同源物-1(LRH-1,命名为NR5A2)是果蝇分节基因(dFTZ-F1)的哺乳动物同源物,在结构上属于孤儿核受体超家族。LRH-1能够识别DNA序列5'-AAGGTCA-3',这是类固醇生成因子1(SF-1)的典型识别基序。在此,我们推测LRH-1可能在人类肾上腺类固醇生成酶表达的调节中发挥作用。为了验证这一假设,我们通过逆转录聚合酶链反应(RT-PCR)分析检测了LRH-1在人类成人及胎儿肾上腺中的表达。利用RT-PCR观察到胎儿和成人肾上腺以及肝脏和胰腺均表达LRH-1信使核糖核酸(mRNA)。随后,我们使用H295R肾上腺细胞系检测了LRH-1增强人类11β-羟化酶(hCYP11B1)编码基因转录的能力。将LRH-1与hCYP11B1荧光素酶启动子构建体共转染导致荧光素酶活性诱导增加25倍。此外,共转染含有SF-1结合顺式元件突变的hCYP11B1报告构建体消除了SF-1和LRH-1的刺激作用。电泳迁移率变动分析(EMSA)表明LRH-1能够结合SF-1反应元件。综上所述,我们的数据表明LRH-1在肾上腺中表达,并且可以替代SF-1来增强某些类固醇代谢酶编码基因的转录。LRH-1在肾上腺或性腺类固醇激素产生调节中的作用有待进一步研究。