Liu Yi-Wen, Gao Wei, Teh Hui-Ling, Tan Jee-Hian, Chan Woon-Khiong
Department of Biological Sciences, National University of Singapore, Singapore 117543, Republic of Singapore.
Mol Cell Biol. 2003 Oct;23(20):7243-55. doi: 10.1128/MCB.23.20.7243-7255.2003.
Steroidogenic factor 1 (SF-1) plays an essential role in adrenal development, although the exact molecular mechanisms are unclear. Our previous work established that Ff1b is the zebra fish homologue of SF-1 and that its disruption by antisense morpholinos leads to a complete ablation of the interrenal organ. In this study, results of biochemical analyses suggest that Ff1b and other Ff1 members interact with Prox1, a homeodomain protein. Fine mapping using site-directed mutants showed that this interaction requires an intact Ff1b heptad 9 and AF2, as well as Prox1 NR Box I. In vivo, this physical interaction led to the inhibition of Ff1-mediated transactivation of pLuc3XFRE, indicating that Prox1 acts to repress the transcriptional activity of Ff1b. In situ hybridization demonstrates that prox1 colocalizes with ff1a and ff1b in the liver and interrenal primordia, respectively. Embryos microinjected with prox1 morpholino displayed a consistent partial reduction of 3 eta-Hsd activity in the interrenal organ, while ff1b morpholino led to a disappearance of prox1. Based on these results, we propose that during the course of interrenal organogenesis, Prox1 functions as a tissue-specific coregulator of Ff1b and that the subsequent inhibition of Ff1b activity, after its initial roles in the specification of interrenal primordium, is critical for the maturation of the interrenal organ.
类固醇生成因子1(SF-1)在肾上腺发育中起着至关重要的作用,尽管确切的分子机制尚不清楚。我们之前的研究确定Ff1b是SF-1的斑马鱼同源物,并且反义吗啉代寡核苷酸对其的破坏会导致肾间组织完全缺失。在本研究中,生化分析结果表明Ff1b和其他Ff1成员与一种同源结构域蛋白Prox1相互作用。使用定点突变体进行的精细定位表明,这种相互作用需要完整的Ff1b七肽9和AF2以及Prox1 NR Box I。在体内,这种物理相互作用导致Ff1介导的pLuc3XFRE反式激活受到抑制,表明Prox1起到抑制Ff1b转录活性的作用。原位杂交显示prox1分别与肝脏和肾间原基中的ff1a和ff1b共定位。显微注射prox1吗啉代寡核苷酸的胚胎在肾间组织中3 eta-Hsd活性持续出现部分降低,而ff1b吗啉代寡核苷酸则导致prox1消失。基于这些结果,我们提出在肾间器官发生过程中,Prox1作为Ff1b的组织特异性共调节因子发挥作用,并且在其最初在肾间原基特化中发挥作用后,对Ff1b活性的后续抑制对于肾间器官的成熟至关重要。