Kuwabara Tomoko, Hsieh Jenny, Nakashima Kinichi, Warashina Masaki, Taira Kazunari, Gage Fred H
Gene Function Research Center, National Institute of Advanced Industrial Science and Technology, Tsukuba 305-8562, Japan.
Nucleic Acids Symp Ser (Oxf). 2005(49):87-8. doi: 10.1093/nass/49.1.87.
Recently we found that the nuclear localized small modulatory double-stranded (ds) RNA (smRNA) coding NRSE sequences triggered activation of transcription of NRSE genes in adult hippocampal neural stem cells. NRSE smRNA, which are non-coding dsRNAs about 20 bp in length, reside in the nucleus and play a critical role in mediating neuronal differentiation. These smRNAs carry the sequence of NRSE/RE1, which is recognized by the NRSF/REST transcription factor. The NRSE sequences are embedded widely in the genomic region, typically in promoters of neuron-specific genes. The mechanism of action appears to be mediated through a specific interaction between dsRNA and DNA/protein interaction, rather than through siRNA or miRNA. The discovery of smRNAs extends the important contribution of non-coding RNAs as key regulators of cell fate choice for adult neurogenesis.
最近我们发现,编码NRSE序列的核定位小调节双链(ds)RNA(smRNA)可触发成年海马神经干细胞中NRSE基因转录的激活。NRSE smRNA是长度约为20 bp的非编码dsRNA,存在于细胞核中,并在介导神经元分化中起关键作用。这些smRNA携带NRSE/RE1序列,该序列可被NRSF/REST转录因子识别。NRSE序列广泛嵌入基因组区域,通常位于神经元特异性基因的启动子中。其作用机制似乎是通过dsRNA与DNA/蛋白质相互作用之间的特异性相互作用介导的,而不是通过siRNA或miRNA。smRNA的发现扩展了非编码RNA作为成年神经发生细胞命运选择关键调节因子的重要贡献。