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一段小的调节性双链RNA决定成年神经干细胞的命运。

A small modulatory dsRNA specifies the fate of adult neural stem cells.

作者信息

Kuwabara Tomoko, Hsieh Jenny, Nakashima Kinichi, Taira Kazunari, Gage Fred H

机构信息

Laboratory of Genetics, The Salk Institute, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Cell. 2004 Mar 19;116(6):779-93. doi: 10.1016/s0092-8674(04)00248-x.

Abstract

Discovering the molecular mechanisms that regulate neuron-specific gene expression remains a central challenge for CNS research. Here, we report that small, noncoding double-stranded (ds) RNAs play a critical role in mediating neuronal differentiation. The sequence defined by this dsRNA is NRSE/RE1, which is recognized by NRSF/REST, known primarily as a negative transcriptional regulator that restricts neuronal gene expression to neurons. The NRSE dsRNA can trigger gene expression of neuron-specific genes through interaction with NRSF/REST transcriptional machinery, resulting in the transition from neural stem cells with neuron-specific genes silenced by NRSF/REST into cells with neuronal identity that can express neuronal genes. The mechanism of action appears to be mediated through a dsRNA/protein interaction, rather than through siRNA or miRNA. The discovery of small modulatory dsRNAs (smRNAs) extends the important contribution of noncoding RNAs as key regulators of cell behavior at both transcriptional and posttranscriptional levels.

摘要

发现调控神经元特异性基因表达的分子机制仍然是中枢神经系统研究的核心挑战。在此,我们报告小的非编码双链(ds)RNA在介导神经元分化中起关键作用。这种dsRNA所定义的序列是NRSE/RE1,它被NRSF/REST识别,NRSF/REST主要作为一种负性转录调节因子,将神经元基因表达限制在神经元中。NRSE dsRNA可通过与NRSF/REST转录机制相互作用触发神经元特异性基因的表达,导致神经元特异性基因被NRSF/REST沉默的神经干细胞转变为具有神经元特性且能表达神经元基因的细胞。其作用机制似乎是通过dsRNA/蛋白质相互作用介导的,而不是通过siRNA或miRNA。小调节性dsRNA(smRNA)的发现扩展了非编码RNA作为转录和转录后水平细胞行为关键调节因子的重要作用。

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