Laboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba, 277-8562, Japan.
Sci Rep. 2020 Dec 8;10(1):21450. doi: 10.1038/s41598-020-78452-6.
The fovea is a pit formed in the center of the retina that enables high-acuity vision in certain vertebrate species. While formation of the fovea fascinates many researchers, the molecular mechanisms underlying foveal development are poorly understood. In the current study, we histologically investigated foveal development in zebra finch (Taeniopygia guttata) and found that foveal pit formation begins just before post-hatch day 14 (P14). We next performed RNA-seq analysis to compare gene expression profiles between the central (foveal and parafoveal) and peripheral retina in zebra finch at P14. We found that the Arhgef33 expression is enriched in the middle layer of the inner nuclear layer at the parafovea, suggesting that Arhgef33 is dominantly expressed in Müller glial cells in the developing parafovea. We then performed a pull-down assay using Rhotekin-RBD and observed GEF activity of Arhgef33 against RhoA. We found that overexpression of Arhgef33 in HEK293 cells induces cell contraction and that Arhgef33 expression inhibits neurite extension in Neuro 2A cells, which is partially recovered by a Rho-kinase (ROCK) inhibitor. Taken together, we used zebra finch as a model animal to investigate foveal development and identified Arhgef33 as a candidate protein possibly involved in foveal development through modulating RhoA activity.
中央凹是视网膜中心的凹陷,使某些脊椎动物物种具有高敏锐度的视觉。虽然中央凹的形成引起了许多研究人员的兴趣,但中央凹发育的分子机制还了解甚少。在本研究中,我们通过组织学方法研究了斑马雀(Taeniopygia guttata)的中央凹发育,发现中央凹陷的形成始于孵出后第 14 天(P14)之前。接下来,我们进行了 RNA-seq 分析,以比较 P14 时斑马雀中央(中央凹和旁中心)和周边视网膜之间的基因表达谱。我们发现,Arhgef33 在旁中心的内核层中层表达丰富,表明 Arhgef33在发育中的旁中心中主要表达在 Müller 胶质细胞中。然后,我们使用 Rhotekin-RBD 进行了下拉测定,并观察到 Arhgef33 对 RhoA 的 GEF 活性。我们发现,在 HEK293 细胞中过表达 Arhgef33 会诱导细胞收缩,并且 Arhgef33 的表达抑制 Neuro 2A 细胞中的神经突延伸,而 Rho-激酶(ROCK)抑制剂可部分恢复该作用。综上所述,我们使用斑马雀作为模型动物来研究中央凹发育,并确定 Arhgef33 可能通过调节 RhoA 活性参与中央凹发育的候选蛋白。