Rhee M, Dimaculangan D, Berger F G
Department of Biological Sciences, University of South Carolina, Columbia 29208.
Mol Endocrinol. 1991 Apr;5(4):564-72. doi: 10.1210/mend-5-4-564.
Transcription of the RP2 gene in the mouse kidney is induced by androgens. This induction is species specific within the genus Mus. For example, the gene responds to androgens in Mus domesticus, but is refractory to hormone in the distantly related species M. caroli. In the present report we have characterized DNA-binding factors that recognize the 5' flanking region of the RP2 gene. One factor (termed RPBF-1) binds a DNA fragment spanning the region between -157 and -311 relative to the transcriptional start site. RPBF-1 is present in kidney nuclear extracts from both control and androgen-treated M. domesticus as well as from control M. caroli; however, in the latter species a distinct factor (termed RPBF-2) is induced by androgens and replaces RPBF-1. The androgen-dependent replacement of RPBF-1 by RPBF-2 is specific to the kidney of M. caroli. DNase-1 footprinting analyses indicate that the two factors recognize distinct, yet overlapping, regions of the RP2 promoter: RPBF-1 binds the region between -247 and -269, while RPBF-2 binds the region between -265 and -290. The RPBF-2-binding site contains a sequence that is homologous to that recognized by nuclear factor-1 (NF-1), suggesting that RPBF-2 is a NF-1-like factor. This is supported by competition experiments with synthetic oligonucleotides corresponding to the NF-1-binding site within the adenovirus origin of replication. Thus, androgens can modulate, in a species- and tissue-specific manner, DNA-binding factors that recognize promoter regions of genes.(ABSTRACT TRUNCATED AT 250 WORDS)
小鼠肾脏中RP2基因的转录由雄激素诱导。这种诱导在小家鼠属内具有物种特异性。例如,该基因在小家鼠中对雄激素有反应,但在远缘物种卡罗来纳小家鼠中对激素不敏感。在本报告中,我们鉴定了识别RP2基因5'侧翼区域的DNA结合因子。一种因子(称为RPBF-1)结合相对于转录起始位点跨越-157至-311区域的DNA片段。RPBF-1存在于对照和雄激素处理的小家鼠以及对照卡罗来纳小家鼠的肾脏核提取物中;然而,在后者物种中,一种不同的因子(称为RPBF-2)由雄激素诱导并取代RPBF-1。RPBF-2对RPBF-1的雄激素依赖性取代是卡罗来纳小家鼠肾脏特有的。DNase-1足迹分析表明,这两种因子识别RP2启动子的不同但重叠的区域:RPBF-1结合-247至-269之间的区域,而RPBF-2结合-265至-290之间的区域。RPBF-2结合位点包含一个与核因子-1(NF-1)识别的序列同源的序列,表明RPBF-2是一种NF-1样因子。这通过与对应于腺病毒复制起点内NF-1结合位点的合成寡核苷酸的竞争实验得到支持。因此,雄激素可以以物种和组织特异性的方式调节识别基因启动子区域的DNA结合因子。(摘要截断于250字)