Nagai T, Aruga J, Minowa O, Sugimoto T, Ohno Y, Noda T, Mikoshiba K
Molecular Neurobiology Laboratory, Tsukuba Life Science Center, RIKEN, Tsukuba, Ibaraki 305-0074, Japan.
Proc Natl Acad Sci U S A. 2000 Feb 15;97(4):1618-23. doi: 10.1073/pnas.97.4.1618.
Mutation in human ZIC2, a zinc finger protein homologous to Drosophila odd-paired, causes holoprosencephaly (HPE), which is a common, severe malformation of the brain in humans. However, the pathogenesis is largely unknown. Here we show that reduced expression (knockdown) of mouse Zic2 causes neurulation delay, resulting in HPE and spina bifida. Differentiation of the most dorsal neural plate, which gives rise to both roof plate and neural crest cells, also was delayed as indicated by the expression lag of a roof plate marker, Wnt3a. In addition the development of neural crest derivatives such as dorsal root ganglion was impaired. These results suggest that the Zic2 expression level is crucial for the timing of neurulation. Because the Zic2 knockdown mouse is the first mutant with HPE and spina bifida to survive to the perinatal period, the mouse will promote analyses of not only the neurulation but also the pathogenesis of human HPE.
人类ZIC2基因发生突变会导致全前脑畸形(HPE),ZIC2是一种与果蝇odd-paired基因同源的锌指蛋白,全前脑畸形是人类常见的严重脑部畸形。然而,其发病机制在很大程度上尚不清楚。在此我们表明,小鼠Zic2基因表达降低(敲低)会导致神经胚形成延迟,进而导致全前脑畸形和脊柱裂。最背侧神经板的分化会产生顶板和神经嵴细胞,正如顶板标志物Wnt3a的表达滞后所示,这种分化也会延迟。此外,神经嵴衍生物如背根神经节的发育也受到损害。这些结果表明,Zic2基因的表达水平对于神经胚形成的时间至关重要。由于Zic2基因敲低小鼠是首个患有全前脑畸形和脊柱裂且存活至围产期的突变体,该小鼠将不仅促进对神经胚形成的分析,还将推动对人类全前脑畸形发病机制的研究。