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本文引用的文献

1
Increased Expression of Transcription Factor SRY-box-Containing Gene 11 (Sox11) Enhances Neurite Growth by Regulating Neurotrophic Factor Responsiveness.转录因子 SRY-box 基因 11(Sox11)表达增加通过调节神经营养因子反应增强神经突生长。
Neuroscience. 2018 Jul 1;382:93-104. doi: 10.1016/j.neuroscience.2018.04.037. Epub 2018 May 8.
2
Long ncRNA A-ROD activates its target gene DKK1 at its release from chromatin.长链非编码 RNA A-ROD 在从染色质释放时激活其靶基因 DKK1。
Nat Commun. 2018 Apr 24;9(1):1636. doi: 10.1038/s41467-018-04100-3.
3
Intrinsic mechanisms of neuronal axon regeneration.神经元轴突再生的内在机制。
Nat Rev Neurosci. 2018 Jun;19(6):323-337. doi: 10.1038/s41583-018-0001-8.
4
Single-nucleus analysis of accessible chromatin in developing mouse forebrain reveals cell-type-specific transcriptional regulation.对发育中的小鼠前脑可及染色质进行单核分析,揭示了细胞类型特异性转录调控。
Nat Neurosci. 2018 Mar;21(3):432-439. doi: 10.1038/s41593-018-0079-3. Epub 2018 Feb 12.
5
The long non-coding RNA contributes to SOX9 expression and chondrogenic differentiation of human mesenchymal stem cells.长链非编码RNA有助于人骨髓间充质干细胞的SOX9表达和软骨分化。
Development. 2017 Dec 15;144(24):4510-4521. doi: 10.1242/dev.152504. Epub 2017 Oct 30.
6
Multiscale 3D Genome Rewiring during Mouse Neural Development.小鼠神经发育过程中的多尺度3D基因组重排
Cell. 2017 Oct 19;171(3):557-572.e24. doi: 10.1016/j.cell.2017.09.043.
7
Non-coding Transcription Instructs Chromatin Folding and Compartmentalization to Dictate Enhancer-Promoter Communication and T Cell Fate.非编码转录指导染色质折叠和区室化以决定增强子-启动子通讯及T细胞命运。
Cell. 2017 Sep 21;171(1):103-119.e18. doi: 10.1016/j.cell.2017.09.001.
8
Neuroregeneration using cellular reprogramming.利用细胞重编程进行神经再生。
Neural Regen Res. 2017 Jul;12(7):1073-1074. doi: 10.4103/1673-5374.211182.
9
Enhanced Neuronal Regeneration in the CAST/Ei Mouse Strain Is Linked to Expression of Differentiation Markers after Injury.CAST/Ei小鼠品系中增强的神经元再生与损伤后分化标志物的表达有关。
Cell Rep. 2017 Aug 1;20(5):1136-1147. doi: 10.1016/j.celrep.2017.07.010.
10
Validity and reliability of the CatWalk system as a static and dynamic gait analysis tool for the assessment of functional nerve recovery in small animal models.CatWalk 系统作为一种静态和动态步态分析工具,用于评估小动物模型中功能性神经恢复的有效性和可靠性。
Brain Behav. 2017 May 18;7(7):e00723. doi: 10.1002/brb3.723. eCollection 2017 Jul.

长非编码 RNA 对神经再生的调控。

Regulation of Neuroregeneration by Long Noncoding RNAs.

机构信息

Department of Biological Regulation, Weizmann Institute of Science, Rehovot 76100, Israel.

Department of Biological Regulation, Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

Mol Cell. 2018 Nov 1;72(3):553-567.e5. doi: 10.1016/j.molcel.2018.09.021. Epub 2018 Oct 25.

DOI:10.1016/j.molcel.2018.09.021
PMID:30401432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6542662/
Abstract

In mammals, neurons in the peripheral nervous system (PNS) have regenerative capacity following injury, but it is generally absent in the CNS. This difference is attributed, at least in part, to the intrinsic ability of PNS neurons to activate a unique regenerative transcriptional program following injury. Here, we profiled gene expression following sciatic nerve crush in mice and identified long noncoding RNAs (lncRNAs) that act in the regenerating neurons and which are typically not expressed in other contexts. We show that two of these lncRNAs regulate the extent of neuronal outgrowth. We then focus on one of these, Silc1, and show that it regulates neuroregeneration in cultured cells and in vivo, through cis-acting activation of the transcription factor Sox11.

摘要

在哺乳动物中,外周神经系统 (PNS) 的神经元在受伤后具有再生能力,但在中枢神经系统 (CNS) 中通常不存在。这种差异至少部分归因于 PNS 神经元在受伤后激活独特的再生转录程序的内在能力。在这里,我们对小鼠坐骨神经挤压后的基因表达进行了分析,鉴定了在再生神经元中起作用的长非编码 RNA(lncRNA),这些 lncRNA 在其他情况下通常不表达。我们表明,其中两个 lncRNA 调节神经元生长的程度。然后,我们将重点放在其中之一 Silc1 上,并表明它通过 Sox11 转录因子的顺式激活来调节培养细胞和体内的神经再生。