Child Study Center, Yale School of Medicine, New Haven, CT 06510, USA.
Department of Biostatistics, Yale School of Public Health, New Haven, CT 06510, USA.
Cell Rep. 2023 Mar 28;42(3):112243. doi: 10.1016/j.celrep.2023.112243. Epub 2023 Mar 17.
Advancing from gene discovery in autism spectrum disorders (ASDs) to the identification of biologically relevant mechanisms remains a central challenge. Here, we perform parallel in vivo functional analysis of 10 ASD genes at the behavioral, structural, and circuit levels in zebrafish mutants, revealing both unique and overlapping effects of gene loss of function. Whole-brain mapping identifies the forebrain and cerebellum as the most significant contributors to brain size differences, while regions involved in sensory-motor control, particularly dopaminergic regions, are associated with altered baseline brain activity. Finally, we show a global increase in microglia resulting from ASD gene loss of function in select mutants, implicating neuroimmune dysfunction as a key pathway relevant to ASD biology.
从自闭症谱系障碍(ASD)的基因发现推进到生物相关机制的鉴定仍然是一个核心挑战。在这里,我们在斑马鱼突变体中平行地进行了 10 个 ASD 基因的行为、结构和回路水平的功能分析,揭示了基因功能丧失的独特和重叠影响。全脑映射确定了前脑和小脑是大脑大小差异的最重要贡献者,而参与感觉运动控制的区域,特别是多巴胺能区域,与改变基线大脑活动有关。最后,我们发现一些特定突变体中 ASD 基因功能丧失会导致小胶质细胞的全面增加,这表明神经免疫功能障碍是与 ASD 生物学相关的关键途径。