Department of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA.
Development. 2021 Nov 15;148(22). doi: 10.1242/dev.199584.
Organization of neuronal connections into topographic maps is essential for processing information. Yet, our understanding of topographic mapping has remained limited by our inability to observe maps forming and refining directly in vivo. Here, we used Cre-mediated recombination of a new colorswitch reporter in zebrafish to generate the first transgenic model allowing the dynamic analysis of retinotectal mapping in vivo. We found that the antero-posterior retinotopic map forms early but remains dynamic, with nasal and temporal retinal axons expanding their projection domains over time. Nasal projections initially arborize in the anterior tectum but progressively refine their projection domain to the posterior tectum, leading to the sharpening of the retinotopic map along the antero-posterior axis. Finally, using a CRISPR-mediated mutagenesis approach, we demonstrate that the refinement of nasal retinal projections requires the adhesion molecule Contactin 2. Altogether, our study provides the first analysis of a topographic map maturing in real time in a live animal and opens new strategies for dissecting the molecular mechanisms underlying precise topographic mapping in vertebrates.
神经元连接的拓扑组织对于信息处理至关重要。然而,由于我们无法直接在体内观察到地图的形成和细化,我们对拓扑映射的理解仍然有限。在这里,我们使用斑马鱼中的一种新的颜色开关报告基因的 Cre 介导重组,生成了第一个允许在体内动态分析视网膜-顶盖映射的转基因模型。我们发现,前-后视网膜拓扑图形成得较早,但仍然具有动态性,鼻侧和颞侧视网膜轴突随着时间的推移扩展其投射区域。鼻侧投射最初在顶盖的前区分支,但随着时间的推移逐渐细化其投射区域到顶盖的后区,导致沿着前后轴的视网膜拓扑图的锐化。最后,我们使用 CRISPR 介导的诱变方法证明,鼻侧视网膜投射的细化需要黏附分子 Contactin 2。总之,我们的研究提供了在活体动物中实时成熟的拓扑图的首次分析,并为解析脊椎动物中精确拓扑映射的分子机制开辟了新的策略。