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神经基因 2- Tbr2 轴在神经干细胞中形成与神经发生基因表达状态的连续过渡。

The Neurog2-Tbr2 axis forms a continuous transition to the neurogenic gene expression state in neural stem cells.

机构信息

Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0871, Japan.

RIKEN Center for Brain Science, Wako 351-0198, Japan; Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.

出版信息

Dev Cell. 2024 Aug 5;59(15):1913-1923.e6. doi: 10.1016/j.devcel.2024.04.019. Epub 2024 May 20.

Abstract

Neural stem cells (NSCs) differentiate into neuron-fated intermediate progenitor cells (IPCs) via cell division. Although differentiation from NSCs to IPCs is a discrete process, recent transcriptome analyses identified a continuous transcriptional trajectory during this process, raising the question of how to reconcile these contradictory observations. In mouse NSCs, Hes1 expression oscillates, regulating the oscillatory expression of the proneural gene Neurog2, while Hes1 expression disappears in IPCs. Thus, the transition from Hes1 oscillation to suppression is involved in the differentiation of NSCs to IPCs. Here, we found that Neurog2 oscillations induce the accumulation of Tbr2, which suppresses Hes1 expression, generating an IPC-like gene expression state in NSCs. In the absence of Tbr2, Hes1 expression is up-regulated, decreasing the formation of IPCs. These results indicate that the Neurog2-Tbr2 axis forms a continuous transcriptional trajectory to an IPC-like neurogenic state in NSCs, which then differentiate into IPCs via cell division.

摘要

神经干细胞 (NSCs) 通过细胞分裂分化为神经元定向的中间祖细胞 (IPCs)。尽管 NSCs 向 IPCs 的分化是一个离散的过程,但最近的转录组分析在这个过程中鉴定出了一个连续的转录轨迹,这就提出了如何调和这些相互矛盾的观察结果的问题。在小鼠 NSCs 中,Hes1 表达呈振荡模式,调节神经前体细胞基因 Neurog2 的振荡表达,而 Hes1 表达在 IPCs 中消失。因此,NSCs 向 IPCs 分化过程中涉及 Hes1 振荡向抑制的转变。在这里,我们发现 Neurog2 振荡诱导 Tbr2 的积累,Tbr2 抑制 Hes1 的表达,从而在 NSCs 中产生 IPC 样基因表达状态。在缺乏 Tbr2 的情况下,Hes1 的表达上调,减少了 IPC 的形成。这些结果表明,Neurog2-Tbr2 轴在 NSCs 中形成了一个连续的转录轨迹,向 IPC 样神经发生状态分化,然后通过细胞分裂分化为 IPCs。

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