Institute of Structural and Molecular Biology, University College London, Gower Street, London, England WC1E 6BT, UK.
Gene. 2011 Sep 15;484(1-2):69-74. doi: 10.1016/j.gene.2011.06.003. Epub 2011 Jun 12.
During limb regeneration in salamanders the blastemal cells give rise only to structures distal to the level of amputation. This proximodistal identity can be regulated by ectopic expression of Meis homeoproteins or the three finger protein Prod 1 which acts at the cell surface. It has been suggested that Meis acts by regulating the transcription of Prod 1. We have sequenced the axolotl Prod 1 promoter and selected two candidate sites for binding Meis homeoproteins. The sites were mutated in various combinations in promoters expressing a luciferase reporter gene. The promoter activity was assayed by nucleofecting AL1 cells, a cultured axolotl limb cell line that expresses both Prod 1 and Meis 1 and 2. The activity of the promoter was inhibited by 60% after mutation at Meis site 1, but not at Meis site 2. The promoter constructs were electroporated into axolotl limb blastemas and the wild type promoter was more active in a proximal blastema than in a contralateral distal blastema. The wild type promoter was significantly more active than a (site 1+site 2) mutant promoter in contralateral proximal blastemas, but the promoters were equivalent in contralateral distal blastemas. The separate site 1 or site 2 mutants were not significantly different from wild type in contralateral proximal blastemas, thus contrasting with the site 1 results in AL1 cells. These data provide strong support for the hypotheses that the Prod 1 promoter is regulated on the proximodistal axis, and that Meis homeoproteins directly regulate the promoter on this axis during limb regeneration in addition to cultured cells.
在蝾螈肢体再生过程中,芽基细胞仅产生位于截肢水平远端的结构。这种远近端身份可以通过异位表达 Meis 同源蛋白或三指蛋白 Prod1 来调节,后者在细胞表面起作用。有人认为,Meis 通过调节 Prod1 的转录来发挥作用。我们已经对蝾螈 Prod1 启动子进行了测序,并选择了两个候选结合位点用于结合 Meis 同源蛋白。在表达荧光素酶报告基因的启动子中,以各种组合突变了这些位点。通过核转染表达 Prod1 和 Meis1 和 2 的培养的蝾螈肢体细胞系 AL1 细胞,检测启动子的活性。在突变 Meis 位点 1 后,启动子活性抑制了 60%,但在突变 Meis 位点 2 后没有。将启动子构建体电穿孔到蝾螈肢体芽基中,野生型启动子在近端芽基中的活性高于对侧远端芽基。野生型启动子在对侧近端芽基中的活性显著高于(位点 1+位点 2)突变启动子,但在对侧远端芽基中,两者相当。单独的位点 1 或位点 2 突变体在对侧近端芽基中与野生型没有显著差异,这与 AL1 细胞中的位点 1 结果形成对比。这些数据为以下假设提供了有力支持:即 Prod1 启动子在远近轴上受到调节,并且在肢体再生过程中,Meis 同源蛋白除了在培养细胞中外,还直接调节该轴上的启动子。