Differentiation of neural stem cells (NSCs) to neurons requires the activation of genes controlled by the repressor element 1 (RE1) silencing transcription factor (REST)/neuron-restrictive silencer factor (NRSF) protein complex. Important components of REST/NRSF are phosphatases (termed RNA polymerase II C-terminal domain small phosphatases [CTDSPs]) that inhibit RNA polymerase II and suppress neuronal gene expression in NSCs. Activation of genes controlled by CTDSPs is required for neurogenesis, but how this is achieved is not fully understood. Here we show that ctdsp2 is a target of miR-26b, a microRNA that is encoded in an intron of the ctdsp2 primary transcript. This intrinsic negative feedback loop is inactive in NSCs because miR-26b biogenesis is inhibited at the precursor level. Generation of mature miR-26b is activated during neurogenesis, where it suppresses Ctdsp2 protein expression and is required for neuronal cell differentiation in vivo.
Intronic miR-26b controls neuronal differentiation by repressing its host transcript, ctdsp2.
内含子 miR-26b 通过抑制其宿主转录本 ctdsp2 来控制神经元分化
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作者:Dill Holger, Linder Bastian, Fehr Alexander, Fischer Utz
| 期刊: | Genes & Development | 影响因子: | 7.700 |
| 时间: | 2012 | 起止号: | 2012 Jan 1; 26(1):25-30 |
| doi: | 10.1101/gad.177774.111 | 研究方向: | 神经科学 |
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