Huang Yu-Ting, Mason John O, Price David J
Centre for Integrative Physiology, University of Edinburgh, Hugh Robson Building, George Square, Edinburgh, EH8 9XD, UK.
BMC Neurosci. 2017 Jun 5;18(1):47. doi: 10.1186/s12868-017-0365-0.
We studied whether regulation of Cdca7 (Cell division cycle associated 7) expression by transcription factor Pax6 contributes to Pax6's cellular actions during corticogenesis. The function of Cdca7 in mediating Pax6's effects during corticogenesis has not been explored. Pax6 is expressed by radial glial progenitors in the ventricular zone of the embryonic cortical neuroepithelium, where it is required for the development of a normal complement of Tbr2-expressing intermediate progenitor cells in the subventricular zone. Pax6's expression levels are graded across the ventricular zone, with highest levels laterally where Tbr2-expressing progenitors are generated in greatest numbers at early stages of corticogenesis.
We used in situ hybridization and immunohistochemistry to analyse patterns of Cdca7 and Pax6 expression in cortical tissue from wild-type and Pax6 embryos. In each genotype we compared the graded expression of the two genes quantitatively at several ages. To test whether defects in Cdca7 expression in lateral cortical cells might contribute to the cellular defects in this region caused by Pax6 loss, we electroporated a Cdca7 expression vector into wild-type lateral cortex and examined the effect on the production of Tbr2-expressing cells.
We found that Cdca7 is co-expressed with Pax6 in cortical progenitors, at levels opposite to those of Pax6. Lowest levels of Cdca7 are found in the radial glial progenitors of lateral cortex, where Pax6 levels are highest. Higher levels of Cdca7 are found in ventral telencephalon, where Pax6 levels are low. Loss of Pax6 causes Cdca7 expression to increase in the lateral cortex. Elevating Cdca7 in normal lateral cortical progenitors to levels close to those normally found in ventral telencephalon reduces their production of Tbr2-expressing cells early in lateral cortical formation.
Our results suggest that Pax6 normally represses Cdca7 expression in the lateral cortex and that repression of Cdca7 in cells of this region is required for their production of a normal complement of Tbr2-expressing intermediate progenitors.
我们研究了转录因子Pax6对细胞分裂周期相关蛋白7(Cdca7)表达的调控是否有助于Pax6在皮质发生过程中的细胞作用。尚未探究Cdca7在介导皮质发生过程中Pax6效应方面的功能。Pax6由胚胎皮质神经上皮脑室区的放射状胶质祖细胞表达,在脑室下区,它是正常数量表达Tbr2的中间祖细胞发育所必需的。Pax6的表达水平在脑室区呈梯度分布,在皮质发生早期,表达Tbr2的祖细胞数量最多的外侧区域,其表达水平最高。
我们使用原位杂交和免疫组化分析野生型和Pax6基因敲除胚胎皮质组织中Cdca7和Pax6的表达模式。在每种基因型中,我们在几个年龄段定量比较了这两个基因的梯度表达。为了测试外侧皮质细胞中Cdca7表达缺陷是否可能导致Pax6缺失引起的该区域细胞缺陷,我们将Cdca7表达载体电穿孔导入野生型外侧皮质,并检查对表达Tbr2细胞产生的影响。
我们发现Cdca7与Pax6在皮质祖细胞中共同表达,其水平与Pax6相反。在外侧皮质的放射状胶质祖细胞中Cdca7水平最低,而Pax6水平最高。在腹侧端脑中Cdca7水平较高,而Pax6水平较低。Pax6的缺失导致外侧皮质中Cdca7表达增加。将正常外侧皮质祖细胞中的Cdca7水平提高到接近腹侧端脑正常水平,会在外侧皮质形成早期减少其表达Tbr2细胞的产生。
我们的结果表明,Pax6通常抑制外侧皮质中Cdca7的表达,并且该区域细胞中Cdca7的抑制对于其产生正常数量的表达Tbr2的中间祖细胞是必需的。