Britz Olivier, Mattar Pierre, Nguyen Laurent, Langevin Lisa-Marie, Zimmer Céline, Alam Sharmila, Guillemot François, Schuurmans Carol
Division of Molecular Neurobiology, National Institute for Medical Research, The Ridgeway, Mill Hill, London, UK.
Cereb Cortex. 2006 Jul;16 Suppl 1:i138-51. doi: 10.1093/cercor/bhj168.
We showed previously that the proneural genes Neurogenin1 (Ngn1) and Ngn2 are required to specify the phenotypes of early- and not late-born neurons in the neocortex, acting in part through repression of Mash1, a third cortically expressed proneural gene. The precise timing of Ngn1/2 specification activity was unexpected given these genes are expressed throughout cortical development, prompting us to search for a later function. Here we reveal that Ngn2 and Mash1 are expressed in a dynamic fashion, acquiring a cell cycle-biased, nonoverlapping distribution, with preferential expression in prospective basal progenitors, during mid corticogenesis. We also identified a new function for Ngn2 during this latter period, demonstrating that it is required to regulate the transit of cortical progenitors from the ventricular zone (VZ) to the subventricular zone. Notably, Ngn2 regulates progenitor maturation at least in part through repression of Mash1 as misexpression of Mash1 strongly enhanced progenitor cell exit from the VZ. Significantly, the ability of Mash1 to promote progenitor cell maturation occurred independently of its ability to respecify cortical cells and is thus a novel function for Mash1. Taken together, these data support a model whereby Ngn2 and Mash1 function together to regulate the zonal distribution of progenitors in the developing neocortex.
我们之前的研究表明,原神经基因神经生成素1(Ngn1)和神经生成素2(Ngn2)是确定新皮层中早出生而非晚出生神经元表型所必需的,部分是通过抑制Mash1发挥作用,Mash1是第三个在皮层表达的原神经基因。鉴于这些基因在整个皮层发育过程中均有表达,Ngn1/2发挥作用的精确时间出乎意料,这促使我们去寻找其后期功能。在此我们发现,Ngn2和Mash1以动态方式表达,在皮层发生中期呈现出偏向细胞周期的、不重叠的分布,在前体基底祖细胞中优先表达。我们还确定了Ngn2在此后期的一项新功能,证明它是调节皮层祖细胞从脑室区(VZ)向室下区过渡所必需的。值得注意的是,Ngn2至少部分通过抑制Mash1来调节祖细胞成熟,因为Mash1的错误表达会强烈增强祖细胞从VZ的迁出。重要的是,Mash1促进祖细胞成熟的能力独立于其重新指定皮层细胞的能力,因此这是Mash1的一项新功能。综上所述,这些数据支持了一个模型,即Ngn2和Mash1共同作用来调节发育中的新皮层中祖细胞的区域分布。