Wong Loksum, Power Namita, Miles Amanda, Tropepe Vincent
Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada M5S 3G5.
Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada M5S 3G5; Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada M5T 3A9; Centre for the Analysis of Genome Evolution and Function, University of Toronto, Toronto, Ontario, Canada M5S 3B2.
Dev Biol. 2015 Jun 15;402(2):216-28. doi: 10.1016/j.ydbio.2015.03.020. Epub 2015 Apr 11.
Understanding the mechanisms that regulate the transition between the proliferative and a post-mitotic state of retinal progenitor cells (RPCs) is key to advancing our knowledge of retinal growth and maturation. In the present study we determined that during zebrafish embryonic retinal neurogenesis, two paired-type homeobox genes - vsx2 and dmbx1 - function in a mutually antagonistic manner. We demonstrate that vsx2 gene expression requires active Fgf signaling and that this in turn suppresses dmbx1 expression and maintains cells in an undifferentiated, proliferative RPC state. This vsx2-dependent RPC state can be prolonged cell-autonomously by knockdown of dmbx1, or it can be suppressed prematurely by the over-expression of dmbx1, which we show can inhibit vsx2 expression and lead to precocious neuronal differentiation. dmbx1 loss of function also results in altered expression of canonical cell cycle genes, and in particular up-regulation of ccnd1, which correlates with our previous finding of a prolonged RPC cell cycle. By knocking down ccnd1 and dmbx1 simultaneously, we show that RPCs can overcome this phenotype to exit the cell cycle on time and differentiate normally into retinal neurons. Collectively, our data provide novel insight into the mechanism that enables RPCs to exit the cell cycle through a previously unrecognized antagonistic interaction of two paired-type homeobox genes that are central regulators of an Fgf-vsx2-dmbx1-ccnd1 signaling axis.
了解调节视网膜祖细胞(RPC)增殖状态和有丝分裂后状态转变的机制,是增进我们对视网膜生长和成熟认识的关键。在本研究中,我们确定在斑马鱼胚胎视网膜神经发生过程中,两个配对型同源框基因——vsx2和dmbx1——以相互拮抗的方式发挥作用。我们证明vsx2基因表达需要活跃的Fgf信号传导,而这反过来又抑制dmbx1表达,并使细胞维持在未分化的增殖性RPC状态。通过敲低dmbx1,这种依赖于vsx2的RPC状态可以细胞自主地延长,或者通过过表达dmbx1可以过早地抑制该状态,我们发现过表达dmbx1可以抑制vsx2表达并导致过早的神经元分化。dmbx1功能丧失还会导致经典细胞周期基因表达改变,特别是ccnd1的上调,这与我们之前发现的RPC细胞周期延长相关。通过同时敲低ccnd1和dmbx1,我们表明RPC可以克服这种表型,按时退出细胞周期并正常分化为视网膜神经元。总的来说,我们的数据为一种机制提供了新的见解,该机制使RPC能够通过两个配对型同源框基因以前未被认识的拮抗相互作用退出细胞周期,这两个基因是Fgf-vsx2-dmbx1-ccnd1信号轴的核心调节因子。