The microRNA miR-124 antagonizes the anti-neural REST/SCP1 pathway during embryonic CNS development

被引:539
作者
Visvanathan, Jaya
Lee, Seunghee
Lee, Bora
Lee, Jae W.
Lee, Soo-Kyung [1 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Med, Div Diabet Endocrinol & Metab, Houston, TX 77030 USA
[5] Baylor Coll Med, Huffington Ctr Aging, Houston, TX 77030 USA
[6] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
关键词
miR-124; SCP1; neural tube development; neurogenesis;
D O I
10.1101/gad.1519107
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neuronal gene expression is tightly regulated in developing CNS. Here, we demonstrate the anti-neural function of phosphatase SCP1 (small C-terminal domain phosphatase 1) during development. We further show that the neuron-enriched microRNA miR-124 directly targets SCP1-3' untranslated region (UTR) to suppress SCP1 expression. In developing spinal cord, expression of miR-124 and SCP1 is complementary, and miR-124 antagonism phenocopies SCP1 overexpression and vice versa. In P19 cells, miR-124 suppresses SCP1 expression and induces neurogenesis, and SCP1 counteracts this proneural activity of miR-124. Our results suggest that, during CNS development, timely down-regulation of SCP1 is critical for inducing neurogenesis, and miR-124 contributes to this process at least in part by down- regulating SCP1 expression.
引用
收藏
页码:744 / 749
页数:6
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