转录组
生物
遗传学
自闭症谱系障碍
基因
自闭症
核糖核酸
电池类型
计算生物学
突变
神经发育障碍
RNA序列
细胞
细胞培养
自闭症遗传率
遗传数据
发育障碍
遗传变异
遗传分析
遗传性疾病
作者
Junyeop Daniel Roh,Yukyung Jun,Heesu Jeon,Junyoung Kim,Yunho Yi,Minji Kim,Heejin Cho,Yusang Oh,Heera Moon,Jinkyeong Kim,Seongbin Kim,Jeseung Ryu,Muwon Kang,Jisoo Kim,Yeonghyeon Kim,Yewon Jung,Taesun Yoo,Hyoseon Oh,Hyosang Kim,Chunmei Jin
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-09-17
卷期号:393 (6817): 1250-1257
被引量:1
标识
DOI:10.1126/science.adz6688
摘要
Autism spectrum disorder (ASD) is a neurodevelopmental condition with a strong genetic component. Large-scale human genetic studies have identified >1200 ASD-risk genes. We report a sex-balanced atlas of 1008 prefrontal RNA sequencing (RNA-seq) profiles from 17 mouse lines carrying ASD-risk mutations. Our analysis identified two opposing transcriptomic states. The two groups differed in sex bias, regional specificity, developmental stability, cell type remodeling, and responses to fluoxetine and lithium. Single-nucleus RNA-seq revealed broader cell type remodeling in group 1 than in group 2, and cell type-specific modules showed reciprocal associations that mirrored bulk transcriptomic signatures. The framework classifies independent mouse lines and identifies subgroups with conserved synaptic directionality, supporting molecular stratification.
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