Wang Huihui, Wu Yongqing, Fang Ruiling, Sa Jian, Li Zhi, Cao Hongyan, Cui Yuehua
Division of Health Statistics, School of Public Health, Shanxi Medical University, Taiyuan, China.
Department of Hematology, Taiyuan Central Hospital of Shanxi Medical University, Taiyuan, China.
Front Genet. 2020 Nov 16;11:574543. doi: 10.3389/fgene.2020.574543. eCollection 2020.
The prefrontal cortex (PFC) constitutes a large part of the human central nervous system and is essential for the normal social affection and executive function of humans and other primates. Despite ongoing research in this region, the development of interactions between PFC genes over the lifespan is still unknown. To investigate the conversion of PFC gene interaction networks and further identify hub genes, we obtained time-series gene expression data of human PFC tissues from the Gene Expression Omnibus (GEO) database. A statistical model, loggle, was used to construct time-varying networks and several common network attributes were used to explore the development of PFC gene networks with age. Network similarity analysis showed that the development of human PFC is divided into three stages, namely, fast development period, deceleration to stationary period, and recession period. We identified some genes related to PFC development at these different stages, including genes involved in neuronal differentiation or synapse formation, genes involved in nerve impulse transmission, and genes involved in the development of myelin around neurons. Some of these genes are consistent with findings in previous reports. At the same time, we explored the development of several known KEGG pathways in PFC and corresponding hub genes. This study clarified the development trajectory of the interaction between PFC genes, and proposed a set of candidate genes related to PFC development, which helps further study of human brain development at the genomic level supplemental to regular anatomical analyses. The analytical process used in this study, involving the loggle model, similarity analysis, and central analysis, provides a comprehensive strategy to gain novel insights into the evolution and development of brain networks in other organisms.
前额叶皮质(PFC)构成人类中枢神经系统的很大一部分,对人类和其他灵长类动物的正常社交情感和执行功能至关重要。尽管对该区域的研究一直在进行,但PFC基因在整个生命周期中的相互作用发展仍不清楚。为了研究PFC基因相互作用网络的转变并进一步识别枢纽基因,我们从基因表达综合数据库(GEO)中获取了人类PFC组织的时间序列基因表达数据。使用一种统计模型loggle构建随时间变化的网络,并使用几个常见的网络属性来探索PFC基因网络随年龄的发展。网络相似性分析表明,人类PFC的发育分为三个阶段,即快速发育期、减速至静止期和衰退期。我们在这些不同阶段鉴定了一些与PFC发育相关的基因,包括参与神经元分化或突触形成的基因、参与神经冲动传递的基因以及参与神经元周围髓鞘发育的基因。其中一些基因与先前报告中的发现一致。同时,我们探索了PFC中几个已知KEGG通路的发展以及相应的枢纽基因。本研究阐明了PFC基因相互作用的发育轨迹,并提出了一组与PFC发育相关的候选基因,这有助于在基因组水平上对人类大脑发育进行进一步研究,作为常规解剖分析的补充。本研究中使用的分析过程,包括loggle模型、相似性分析和中心分析,提供了一种全面的策略,以获得对其他生物体大脑网络进化和发育的新见解。