Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200030, China.
Shanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 201108, China.
BMC Genomics. 2024 Oct 29;25(1):1012. doi: 10.1186/s12864-024-10911-0.
Elucidating the dynamics of gene expression across developmental stages, including the genomic characteristics of brain expression during infancy, is pivotal in deciphering human psychiatric and neurological disorders and providing insights into developmental disorders.
Leveraging comprehensive human GWAS associations with temporal and spatial brain expression data, we discovered a distinctive co-expression cluster comprising 897 genes highly expressed specifically during infancy, enriched in functions related to the neuronal system. This gene cluster notably harbors the highest ratio of genes linked to psychiatric and neurological disorders. Through computational analysis, MYT1L emerged as a potential central transcription factor governing these genes. Remarkably, the infancy-specific expressed genes, including SYT1, exhibit prominent colocalization within human accelerated regions. Additionally, chromatin state analysis unveiled prevalent epigenetic markers associated with enhancer-specific modifications. In addition, this cluster of genes has demonstrated to be specifically highly expressed in cell-types including excitatory neurons, medial ganglionic eminence and caudal ganglionic eminence.
This study comprehensively characterizes the genomics and epigenomics of genes specifically expressed during infancy, identifying crucial hub genes and transcription factors. These findings offer valuable insights into early detection strategies and interventions for psychiatric and neurological disorders.
阐明发育阶段基因表达的动态,包括婴儿期大脑表达的基因组特征,对于破解人类精神和神经疾病并深入了解发育障碍至关重要。
利用全面的人类全基因组关联研究与时空大脑表达数据,我们发现了一个独特的共表达簇,包含 897 个在婴儿期特异性高表达的基因,其功能富集与神经元系统相关。这个基因簇显著包含与精神和神经疾病关联的最高比例的基因。通过计算分析,MYT1L 被确定为调控这些基因的潜在核心转录因子。值得注意的是,包括 SYT1 在内的在婴儿期特异性表达的基因,在人类加速区域内表现出明显的共定位。此外,染色质状态分析揭示了与增强子特异性修饰相关的普遍表观遗传标记。此外,该基因簇已被证明在包括兴奋性神经元、内侧神经节隆起和尾状神经节隆起在内的细胞类型中特异性高度表达。
本研究全面描述了婴儿期特异性表达基因的基因组学和表观基因组学特征,确定了关键的枢纽基因和转录因子。这些发现为精神和神经疾病的早期检测策略和干预提供了有价值的见解。