Hornig Julia, Fröb Franziska, Vogl Michael R, Hermans-Borgmeyer Irm, Tamm Ernst R, Wegner Michael
Institut für Biochemie, Emil-Fischer-Zentrum, Universität Erlangen-Nürnberg, Erlangen, Germany.
PLoS Genet. 2013 Oct;9(10):e1003907. doi: 10.1371/journal.pgen.1003907. Epub 2013 Oct 31.
Myelin is essential for rapid saltatory conduction and is produced by Schwann cells in the peripheral nervous system and oligodendrocytes in the central nervous system. In both cell types the transcription factor Sox10 is an essential component of the myelin-specific regulatory network. Here we identify Myrf as an oligodendrocyte-specific target of Sox10 and map a Sox10 responsive enhancer to an evolutionarily conserved element in intron 1 of the Myrf gene. Once induced, Myrf cooperates with Sox10 to implement the myelination program as evident from the physical interaction between both proteins and the synergistic activation of several myelin-specific genes. This is strongly reminiscent of the situation in Schwann cells where Sox10 first induces and then cooperates with Krox20 during myelination. Our analyses indicate that the regulatory network for myelination in oligodendrocytes is organized along similar general principles as the one in Schwann cells, but is differentially implemented.
髓磷脂对于快速跳跃式传导至关重要,它由外周神经系统中的施万细胞和中枢神经系统中的少突胶质细胞产生。在这两种细胞类型中,转录因子Sox10都是髓磷脂特异性调控网络的重要组成部分。在此,我们确定Myrf是Sox10在少突胶质细胞中的特异性靶点,并将一个Sox10反应增强子定位到Myrf基因内含子1中一个进化保守元件上。一旦被诱导,Myrf就会与Sox10协同实施髓鞘形成程序,这从两种蛋白质之间的物理相互作用以及几个髓磷脂特异性基因的协同激活中可见一斑。这强烈让人联想到施万细胞中的情况,即在髓鞘形成过程中,Sox10首先诱导然后与Krox20协同作用。我们的分析表明,少突胶质细胞中髓鞘形成的调控网络与施万细胞中的调控网络遵循相似的一般原则,但具体实施方式有所不同。