Department of Human Genetics, The University of Chicago, Chicago, Illinois 60637, USA;
Genes Dev. 2010 Feb 1;24(3):301-11. doi: 10.1101/gad.1864510. Epub 2010 Jan 15.
The controlling factors that prompt mature oligodendrocytes to myelinate axons are largely undetermined. In this study, we used a forward genetics approach to identify a mutant mouse strain characterized by the absence of CNS myelin despite the presence of abundant numbers of late-stage, process-extending oligodendrocytes. Through linkage mapping and complementation testing, we identified the mutation as a single nucleotide insertion in the gene encoding zinc finger protein 191 (Zfp191), which is a widely expressed, nuclear-localized protein that belongs to a family whose members contain both DNA-binding zinc finger domains and protein-protein-interacting SCAN domains. Zfp191 mutants express an array of myelin-related genes at significantly reduced levels, and our in vitro and in vivo data indicate that mutant ZFP191 acts in a cell-autonomous fashion to disrupt oligodendrocyte function. Therefore, this study demonstrates that ZFP191 is required for the myelinating function of differentiated oligodendrocytes.
促使成熟少突胶质细胞形成髓鞘的控制因素在很大程度上尚未确定。在这项研究中,我们使用正向遗传学方法鉴定了一种突变小鼠品系,其特征是尽管存在大量晚期、延伸过程的少突胶质细胞,但中枢神经系统(CNS)没有髓鞘。通过连锁图谱和互补性测试,我们将突变鉴定为编码锌指蛋白 191(Zfp191)的基因中的单个核苷酸插入,该基因是一种广泛表达的核定位蛋白,属于包含 DNA 结合锌指结构域和蛋白-蛋白相互作用 SCAN 结构域的家族成员。Zfp191 突变体以显著降低的水平表达一系列与髓鞘相关的基因,我们的体外和体内数据表明,突变型 ZFP191 以细胞自主性方式作用以破坏少突胶质细胞功能。因此,这项研究表明 ZFP191 是分化的少突胶质细胞髓鞘形成功能所必需的。