Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA; Huffington Center on Aging, Baylor College of Medicine, Houston, TX 77030, USA.
Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Cell Rep. 2018 Aug 28;24(9):2506-2519. doi: 10.1016/j.celrep.2018.07.090.
Retinal function relies on precisely organized neurons and synapses and a properly patterned vasculature to support them. Alterations in these features can result in vision loss. However, our understanding of retinal organization pathways remains incomplete because of a lack of methods to rapidly identify neuron and vasculature regulators in mammals. Here we developed a pipeline for the identification of neural and synaptic integrity genes by high-throughput retinal screening (INSiGHT) that analyzes candidate expression, vascular patterning, cellular organization, and synaptic arrangement. Using this system, we examined 102 mutant mouse lines and identified 16 unique retinal regulatory genes. Fifteen of these candidates are identified as novel retina regulators, and many (9 of 16) are associated with human neural diseases. These results expand the genetic landscape involved in retinal circuit organization and provide a road map for continued discovery of mammalian retinal regulators and disease-causing alleles.
视网膜功能依赖于精确组织的神经元和突触,以及支持它们的适当模式化血管系统。这些特征的改变会导致视力丧失。然而,由于缺乏快速识别哺乳动物神经元和血管调节因子的方法,我们对视网膜组织途径的理解仍然不完整。在这里,我们通过高通量视网膜筛选(INSiGHT)开发了一种用于鉴定神经和突触完整性基因的方法,该方法分析候选物的表达、血管模式、细胞组织和突触排列。使用该系统,我们检查了 102 个突变小鼠系,并鉴定出 16 个独特的视网膜调节基因。其中 15 个候选基因被鉴定为新的视网膜调节因子,其中许多(16 个中的 9 个)与人类神经疾病相关。这些结果扩展了涉及视网膜回路组织的遗传景观,并为进一步发现哺乳动物视网膜调节因子和致病等位基因提供了路线图。