Planque N, Leconte L, Coquelle F M, Martin P, Saule S
CNRS UMR 146, Institut Curie Section Recherche, Centre Universitaire Bâtiment 110, 91405 Orsay Cedex, France.
J Biol Chem. 2001 Aug 3;276(31):29330-7. doi: 10.1074/jbc.M101812200. Epub 2001 May 11.
Pax-6 and microphthalmia transcription factor (Mitf) are required for proper eye development. Pax-6, expressed in both the neuroretina and pigmented retina, has two DNA-binding domains: the paired domain and the homeodomain. Mice homozygous for Pax-6 mutations are anophthalmic. Mitf, a basic helix-loop-helix leucine zipper (b-HLH-LZ) transcription factor associated with the onset and maintenance of pigmentation, identifies the retinal pigmented epithelium during eye development. Loss of Mitf function results in the formation of an ectopic neuroretina at the expense of the dorsal retinal pigmented epithelium. In the present study, we investigated the interaction between Pax-6 and Mitf. In transient transfection-expression experiments, we found that transactivating effects of Pax-6 and Mitf on their respective target promoters were strongly inhibited by co-transfection of both transcription factors. This repression was due to direct protein/protein interactions involving both Pax-6 DNA-binding domains and the Mitf b-HLH-LZ domain. These results suggest that Pax-6/Mitf interactions may be critical for retinal pigmented epithelium development.
眼部的正常发育需要Pax-6和小眼畸形转录因子(Mitf)。Pax-6在神经视网膜和色素视网膜中均有表达,有两个DNA结合结构域:配对结构域和同源结构域。Pax-6突变的纯合小鼠无眼。Mitf是一种与色素沉着的发生和维持相关的碱性螺旋-环-螺旋亮氨酸拉链(b-HLH-LZ)转录因子,在眼睛发育过程中可识别视网膜色素上皮。Mitf功能丧失会导致以背侧视网膜色素上皮为代价形成异位神经视网膜。在本研究中,我们研究了Pax-6与Mitf之间的相互作用。在瞬时转染-表达实验中,我们发现,共转染这两种转录因子会强烈抑制Pax-6和Mitf对其各自靶启动子的反式激活作用。这种抑制是由于涉及Pax-6的两个DNA结合结构域和Mitf的b-HLH-LZ结构域的直接蛋白质/蛋白质相互作用所致。这些结果表明,Pax-6/Mitf相互作用可能对视网膜色素上皮的发育至关重要。