Diks Sander H, Bink Robert J, van de Water Sandra, Joore Jos, van Rooijen Carina, Verbeek Fons J, den Hertog Jeroen, Peppelenbosch Maikel P, Zivkovic Danica
Department of Cell Biology, University Medical Center Groningen, University of Groningen, NL-9713 AV Groningen, Netherlands.
J Cell Biol. 2006 Aug 14;174(4):581-92. doi: 10.1083/jcb.200601081. Epub 2006 Aug 7.
From a differential display designed to isolate genes that are down-regulated upon differentiation of the central nervous system in Danio rerio embryos, we isolated d-asb11 (ankyrin repeat and suppressor of cytokine signaling box-containing protein 11). Knockdown of the d-Asb11 protein altered the expression of neural precursor genes sox2 and sox3 and resulted in an initial relative increase in proneural cell numbers. This was reflected by neurogenin1 expansion followed by premature neuronal differentiation, as demonstrated by HuC labeling and resulting in reduced size of the definitive neuronal compartment. Forced misexpression of d-asb11 was capable of ectopically inducing sox2 while it diminished or entirely abolished neurogenesis. Overexpression of d-Asb11 in both a pluripotent and a neural-committed progenitor cell line resulted in the stimulus-induced inhibition of terminal neuronal differentiation and enhanced proliferation. We conclude that d-Asb11 is a novel regulator of the neuronal progenitor compartment size by maintaining the neural precursors in the proliferating undifferentiated state possibly through the control of SoxB1 transcription factors.
在一项旨在分离斑马鱼胚胎中枢神经系统分化时下调基因的差异显示实验中,我们分离出了d-asb11(含锚蛋白重复序列和细胞因子信号抑制盒蛋白11)。d-Asb11蛋白的敲低改变了神经前体基因sox2和sox3的表达,并导致神经前体细胞数量最初相对增加。这表现为神经生成素1的扩展,随后是神经元过早分化,如HuC标记所示,并导致最终神经元区室大小减小。d-asb11的强制错误表达能够异位诱导sox2,同时减少或完全消除神经发生。在多能和神经定向祖细胞系中过表达d-Asb11会导致刺激诱导的终末神经元分化抑制和增殖增强。我们得出结论,d-Asb11可能通过控制SoxB1转录因子,使神经前体维持在增殖未分化状态,从而成为神经元祖细胞区室大小的新型调节因子。