Wang Shu-Zong, Dulin Jennifer, Wu Heng, Hurlock Edward, Lee Sang-Eun, Jansson Kyle, Lu Q Richard
Center for Developmental Biology and Kent Waldrep Foundation Center for Basic Neuroscience Research on Nerve Growth and Regeneration, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Development. 2006 Sep;133(17):3389-98. doi: 10.1242/dev.02522.
Molecular mechanisms that control oligodendrocyte myelination during mammalian central nervous system (CNS) development are poorly understood. In this study, we identified Zfp488, an oligodendrocyte-specific zinc-finger transcription regulator, by screening for genes downregulated in the optic nerves of Olig1-null mice. The predicted primary structure of Zfp488 is evolutionarily conserved in vertebrates and invertebrates. In the developing CNS, Zfp488 is specifically expressed in oligodendrocytes but not their precursors. Its expression increases in parallel with that of major myelin genes Mbp and Plp1. Zfp488 is a nuclear protein that possesses transcriptional repression activity. In the developing chick neural tube, Zfp488 can promote oligodendrocyte precursor formation upon Notch activation. In addition, Zfp488 can interact and cooperate with the bHLH transcription factor Olig2 to promote precocious and ectopic oligodendrocyte differentiation. Furthermore, knockdown of Zfp488 via RNAi in an oligodendroglial cell line leads to the downregulation of myelin gene expression. Taken together, these data suggest that Zfp488 functions as an oligodendrocyte-specific transcription co-regulator important for oligodendrocyte maturation and that zinc-finger/bHLH cooperation can serve as a mechanism for oligodendroglial differentiation.
在哺乳动物中枢神经系统(CNS)发育过程中,控制少突胶质细胞髓鞘形成的分子机制仍知之甚少。在本研究中,我们通过筛选Olig1基因敲除小鼠视神经中下调的基因,鉴定出一种少突胶质细胞特异性锌指转录调节因子Zfp488。Zfp488的预测一级结构在脊椎动物和无脊椎动物中具有进化保守性。在发育中的中枢神经系统中,Zfp488在少突胶质细胞中特异性表达,而在其前体细胞中不表达。其表达与主要髓鞘基因Mbp和Plp1的表达平行增加。Zfp488是一种具有转录抑制活性的核蛋白。在发育中的鸡神经管中,Zfp488在Notch激活后可促进少突胶质前体细胞的形成。此外,Zfp488可与bHLH转录因子Olig2相互作用并协同作用,促进早熟和异位少突胶质细胞分化。此外,在少突胶质细胞系中通过RNAi敲低Zfp488会导致髓鞘基因表达下调。综上所述,这些数据表明Zfp488作为一种少突胶质细胞特异性转录共调节因子,对少突胶质细胞成熟很重要,并且锌指/bHLH协同作用可作为少突胶质细胞分化的一种机制。