Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Cells. 2024 May 29;13(11):935. doi: 10.3390/cells13110935.
Rapid information processing in the central nervous system requires the myelination of axons by oligodendrocytes. The transcription factor Sox2 and its close relative Sox3 redundantly regulate the development of myelin-forming oligodendrocytes, but little is known about the underlying molecular mechanisms. Here, we characterized the expression profile of cultured oligodendroglial cells during early differentiation and identified Bcas1, Enpp6, Zfp488 and Nkx2.2 as major downregulated genes upon Sox2 and Sox3 deletion. An analysis of mice with oligodendrocyte-specific deletion of Sox2 and Sox3 validated all four genes as downstream targets in vivo. Additional functional assays identified regulatory regions in the vicinity of each gene that are responsive to and bind both Sox proteins. Bcas1, Enpp6, Zfp488 and Nkx2.2 therefore likely represent direct target genes and major effectors of Sox2 and Sox3. Considering the preferential expression and role of these genes in premyelinating oligodendrocytes, our findings suggest that Sox2 and Sox3 impact oligodendroglial development at the premyelinating stage with Bcas1, Enpp6, Zfp488 and Nkx2.2 as their major effectors.
中枢神经系统的快速信息处理需要少突胶质细胞对轴突进行髓鞘化。转录因子 Sox2 及其密切相关的 Sox3 冗余调节髓鞘形成少突胶质细胞的发育,但对其潜在的分子机制知之甚少。在这里,我们描述了培养的少突胶质细胞在早期分化过程中的表达谱,并鉴定出 Bcas1、Enpp6、Zfp488 和 Nkx2.2 是 Sox2 和 Sox3 缺失后主要下调的基因。对少突胶质细胞特异性缺失 Sox2 和 Sox3 的小鼠进行分析,验证了这四个基因在体内都是下游靶点。额外的功能分析确定了每个基因附近的调控区域,这些区域对 Sox 蛋白有反应并与之结合。因此,Bcas1、Enpp6、Zfp488 和 Nkx2.2 可能代表 Sox2 和 Sox3 的直接靶基因和主要效应物。考虑到这些基因在未成熟的少突胶质细胞中的优先表达和作用,我们的发现表明 Sox2 和 Sox3 在未成熟的少突胶质细胞阶段影响少突胶质细胞的发育,Bcas1、Enpp6、Zfp488 和 Nkx2.2 是它们的主要效应物。