Department of Biomedicine, University of Basel, Mattenstrasse 28, CH-4058, Basel, Switzerland.
Biozentrum, University of Basel, Klingelbergstrasse 50-70, CH-4056, Basel, Switzerland.
Sci Rep. 2020 Mar 13;10(1):4625. doi: 10.1038/s41598-020-61490-5.
Neural stem cells (NSCs) generate neurons of the cerebral cortex with distinct morphologies and functions. How specific neuron production, differentiation and migration are orchestrated is unclear. Hippo signaling regulates gene expression through Tead transcription factors (TFs). We show that Hippo transcriptional coactivators Yap1/Taz and the Teads have distinct functions during cortical development. Yap1/Taz promote NSC maintenance and Satb2 neuron production at the expense of Tbr1 neuron generation. However, Teads have moderate effects on NSC maintenance and do not affect Satb2 neuron differentiation. Conversely, whereas Tead2 blocks Tbr1 neuron formation, Tead1 and Tead3 promote this early fate. In addition, we found that Hippo effectors regulate neuronal migration to the cortical plate (CP) in a reciprocal fashion, that ApoE, Dab2 and Cyr61 are Tead targets, and these contribute to neuronal fate determination and migration. Our results indicate that multifaceted Hippo signaling is pivotal in different aspects of cortical development.
神经干细胞 (NSCs) 产生具有不同形态和功能的大脑皮层神经元。特定神经元的产生、分化和迁移是如何协调的还不清楚。Hippo 信号通过 Tead 转录因子 (TFs) 调节基因表达。我们发现,Hippo 转录共激活因子 Yap1/Taz 和 Teads 在皮质发育过程中具有不同的功能。 Yap1/Taz 促进 NSC 的维持和 Satb2 神经元的产生,而牺牲 Tbr1 神经元的生成。然而,Teads 对 NSC 的维持影响不大,也不影响 Satb2 神经元的分化。相反,Tead2 阻止 Tbr1 神经元的形成,而 Tead1 和 Tead3 则促进这一早期命运。此外,我们发现 Hippo 效应物以相互的方式调节神经元向皮质板 (CP) 的迁移,ApoE、Dab2 和 Cyr61 是 Tead 的靶标,这些靶标有助于神经元命运决定和迁移。我们的结果表明,多方面的 Hippo 信号在皮质发育的不同方面起着关键作用。