State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, MOE Frontier Research Center for Brain Science, Shanghai Key Lab of Birth Defect, Children's Hospital, Fudan University, Shanghai, 200032, P.R. China.
Cell Death Dis. 2021 Mar 12;12(3):262. doi: 10.1038/s41419-021-03552-8.
The striatum is structurally highly diverse, and its organ functionality critically depends on normal embryonic development. Although several studies have been conducted on the gene functional changes that occur during striatal development, a system-wide analysis of the underlying molecular changes is lacking. Here, we present a comprehensive transcriptome profile that allows us to explore the trajectory of striatal development and identify the correlation between the striatal development and Huntington's disease (HD). Furthermore, we applied an integrative transcriptomic profiling approach based on machine learning to systematically map a global landscape of 277 transcription factor (TF) networks. Most of these TF networks are linked to biological processes, and some unannotated genes provide information about the corresponding mechanisms. For example, we found that the Meis2 and Six3 were crucial for the survival of striatal neurons, which were verified using conditional knockout (CKO) mice. Finally, we used RNA-Seq to speculate their downstream targets.
纹状体在结构上高度多样化,其器官功能取决于正常的胚胎发育。尽管已经有几项关于纹状体发育过程中发生的基因功能变化的研究,但对于潜在的分子变化缺乏系统的分析。在这里,我们提供了一个全面的转录组图谱,使我们能够探索纹状体发育的轨迹,并确定纹状体发育与亨廷顿病(HD)之间的相关性。此外,我们应用了一种基于机器学习的综合转录组分析方法,系统地绘制了 277 个转录因子(TF)网络的全局图谱。这些 TF 网络大多数与生物学过程有关,一些未注释的基因提供了相应机制的信息。例如,我们发现 Meis2 和 Six3 对纹状体神经元的存活至关重要,这一点通过条件敲除(CKO)小鼠得到了验证。最后,我们使用 RNA-Seq 来推测它们的下游靶标。