Monuki E S, Kuhn R, Lemke G
Molecular Neurobiology Laboratory, Salk Institute, La Jolla, CA 92037.
Mech Dev. 1993 Jul;42(1-2):15-32. doi: 10.1016/0925-4773(93)90095-f.
SCIP is a POU domain transcription factor expressed by Schwann cells, the myelin-forming glial cells of the peripheral nervous system. In this study, we investigate SCIP regulation of the gene encoding P0, the major structural protein of peripheral myelin. We find that SCIP represses transcription of this gene through the joint action of the SCIP POU domain and an amino terminal domain that acts cell specifically. Maximal repression is DNA-binding-dependent, and analysis of the P0 promoter reveals the presence of multiple SCIP binding sites. Surprisingly, none of these sites in their native positions dramatically affect P0 promoter activity or its repression by SCIP, although they mediate repression when moved closer to the P0 transcription start site. We propose that repression occurs through a quenching mechanism mediated by the SCIP POU and amino terminal domains acting in concert with other nuclear proteins, including a Schwann cell-specific adapter.
SCIP是一种由雪旺细胞表达的POU结构域转录因子,雪旺细胞是周围神经系统中形成髓鞘的神经胶质细胞。在本研究中,我们研究了SCIP对编码P0(周围髓鞘的主要结构蛋白)的基因的调控。我们发现SCIP通过SCIP POU结构域和一个细胞特异性作用的氨基末端结构域的联合作用来抑制该基因的转录。最大程度的抑制依赖于DNA结合,并且对P0启动子的分析揭示了存在多个SCIP结合位点。令人惊讶的是,这些位点在其天然位置时均未显著影响P0启动子活性或SCIP对其的抑制作用,尽管当它们移至更靠近P0转录起始位点时可介导抑制作用。我们提出,抑制作用是通过一种淬灭机制发生的,该机制由SCIP POU和氨基末端结构域与其他核蛋白(包括雪旺细胞特异性衔接蛋白)协同作用介导。