基因组学对婴儿期特异表达基因的深入研究凸显了它们对神经元系统的主导影响。

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Weidi Wang, Zhe Liu, Daihui Peng, Guan Ning Lin, Zhen Wang
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引用次数: 0

摘要

背景:阐明各发育阶段基因表达的动态变化,包括婴儿期大脑表达的基因组特征,对于解读人类精神和神经疾病以及深入研究发育障碍至关重要:利用全面的人类 GWAS 与时间和空间大脑表达数据的关联,我们发现了一个独特的共表达集群,由 897 个在婴儿期特异性高表达的基因组成,富含与神经元系统相关的功能。值得注意的是,该基因簇中与精神和神经疾病相关的基因比例最高。通过计算分析,MYT1L 成为管理这些基因的潜在中心转录因子。值得注意的是,包括 SYT1 在内的婴幼儿特异性表达基因在人类加速区内表现出显著的共定位。此外,染色质状态分析揭示了与增强子特异性修饰相关的流行表观遗传标记。此外,这组基因还被证明在兴奋性神经元、内侧神经节突起和尾神经节突起等细胞类型中特异性高表达:这项研究全面描述了婴儿期特异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措施提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic insights into genes expressed specifically during infancy highlight their dominant influence on the neuronal system.

Background: 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.

Results: 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.

Conclusions: 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.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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