Suppr超能文献

对小鼠皮质祖细胞和神经元的 microRNA 谱分析显示 miR-486-5p 可作为神经发生的调节因子。

MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis.

机构信息

CRTD - Center for Regenerative Therapies Dresden, School of Medicine, TU Dresden, Fetcherstrasse 105, 01307 Dresden, Germany.

DRESDEN-concept Genome Center c/o Center for Molecular and Cellular Bioengineering (CMCB), Technische Universität Dresden, Fetcherstrasse 105, 01307 Dresden, Germany.

出版信息

Development. 2020 May 11;147(9):dev190520. doi: 10.1242/dev.190520.

Abstract

MicroRNAs (miRNAs) are short (∼22 nt) single-stranded non-coding RNAs that regulate gene expression at the post-transcriptional level. Over recent years, many studies have extensively characterized the involvement of miRNA-mediated regulation in neurogenesis and brain development. However, a comprehensive catalog of cortical miRNAs expressed in a cell-specific manner in progenitor types of the developing mammalian cortex is still missing. Overcoming this limitation, here we exploited a double reporter mouse line previously validated by our group to allow the identification of the transcriptional signature of neurogenic commitment and provide the field with the complete atlas of miRNA expression in proliferating neural stem cells, neurogenic progenitors and newborn neurons during corticogenesis. By extending the currently known list of miRNAs expressed in the mouse brain by over twofold, our study highlights the power of cell type-specific analyses for the detection of transcripts that would otherwise be diluted out when studying bulk tissues. We further exploited our data by predicting putative miRNAs and validated the power of our approach by providing evidence for the involvement of miR-486 in brain development.

摘要

微小 RNA(miRNAs)是短链(约 22nt)的单链非编码 RNA,可在转录后水平调控基因表达。近年来,许多研究广泛描述了 miRNA 介导的调节在神经发生和大脑发育中的作用。然而,在发育中的哺乳动物皮质的祖细胞类型中以细胞特异性方式表达的皮质 miRNAs 的综合目录仍然缺失。为了克服这一限制,我们利用了我们小组之前验证的双报告小鼠系,该系允许鉴定神经发生承诺的转录特征,并为增殖性神经干细胞、神经祖细胞和新生神经元在皮质发生过程中的 miRNA 表达完整图谱提供了研究领域。通过将目前已知的在小鼠大脑中表达的 miRNAs 列表扩展了两倍以上,我们的研究强调了细胞类型特异性分析对于检测转录本的重要性,否则在研究批量组织时这些转录本可能会被稀释掉。我们还通过预测潜在的 miRNAs 进一步利用了我们的数据,并通过提供 miR-486 参与大脑发育的证据来验证我们方法的有效性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验