Biological Sciences Platform, Sunnybrook Research Institute, Toronto, ON M4N 3M5, Canada.
Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.
Development. 2018 Oct 1;145(19):dev157719. doi: 10.1242/dev.157719.
Neural progenitors undergo temporal identity transitions to sequentially generate the neuronal and glial cells that make up the mature brain. Proneural genes have well-characterised roles in promoting neural cell differentiation and subtype specification, but they also regulate the timing of identity transitions through poorly understood mechanisms. Here, we investigated how the highly related proneural genes and interact to control the timing of neocortical neurogenesis. We found that acts in an atypical fashion as it is required to suppress rather than promote neuronal differentiation in early corticogenesis. In neocortices, early born neurons differentiate in excess, whereas, , progenitors have a decreased propensity to proliferate and form neurospheres Instead, progenitors preferentially generate neurons, a phenotype restricted to the progenitor pool. Mechanistically, Neurog1 and Neurog2 heterodimerise, and while and individually promote neurogenesis, misexpression together blocks this effect. Finally, is also required to induce the expression of neurogenic factors ( and ) and to repress the expression of neuronal differentiation genes ( and ). thus employs different mechanisms to temper the pace of early neocortical neurogenesis.
神经祖细胞经历时间上的身份转变,依次产生构成成熟大脑的神经元和神经胶质细胞。神经前体细胞基因在促进神经细胞分化和亚型特化方面具有明确的作用,但它们也通过尚未完全了解的机制调节身份转变的时间。在这里,我们研究了高度相关的神经前体细胞基因 和 如何相互作用来控制新皮层神经发生的时间。我们发现, 以一种非典型的方式发挥作用,因为它需要抑制而不是促进早期皮质发生中的神经元分化。在 新皮层中,早期出生的神经元过度分化,而 、 祖细胞增殖和形成神经球的倾向降低。相反, 祖细胞优先产生神经元,这种表型仅限于 祖细胞池。从机制上讲,Neurog1 和 Neurog2 异二聚化,虽然 和 单独促进神经发生,但一起过表达会阻止这种效应。最后, 还需要诱导神经发生因子( 和 )的表达,并抑制神经元分化基因( 和 )的表达。因此, 采用不同的机制来调节早期新皮层神经发生的速度。