Cohesive Regulation of Neural Progenitor Development by microRNA miR-26, Its Host Gene Ctdsp and Target Gene Emx2 in the Mouse Embryonic Cerebral Cortex

被引:16
|
作者
Zhang, Haijun [1 ,2 ]
Zhang, Longbin [3 ,4 ]
Sun, Tao [1 ,3 ,4 ]
机构
[1] Cornell Univ, Dept Cell & Dev Biol, Weill Cornell Med Coll, New York, NY 10021 USA
[2] Cornell Univ, Weill Cornell Med Coll, Dept Med Genet, New York, NY 10021 USA
[3] Huaqiao Univ, Sch Med, Ctr Precis Med, Xiamen, Peoples R China
[4] Huaqiao Univ, Sch Biomed Sci, Xiamen, Peoples R China
来源
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
miR-26; Ctdsp; Emx2; neural progenitor; cell-cycle progression; TERMINAL DOMAIN PHOSPHATASES; CELL-CYCLE PROGRESSION; SMALL RNAS; STEM; GROWTH; NEUROGENESIS; EXPRESSION; DIFFERENTIATION; DIVISION; MIRNAS;
D O I
10.3389/fnmol.2018.00044
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Proper proliferation and differentiation of neural progenitors (NPs) in the developing cerebral cortex are critical for normal brain formation and function. Emerging evidence has shown the importance of microRNAs (miRNAs) in regulating cortical development and the etiology of neurological disorders. Here we show that miR-26 is co-expressed with its host gene Ctdsp in the mouse embryonic cortex. We demonstrate that similar to its host gene Ctdsp2, miR-26 positively regulates proliferation of NPs through controlling the cell-cycle progression, by using miR-26 overexpression and sponge approaches. On the contrary, miR-26 target gene Emx2 limits expansion of cortical NPs, and promotes transcription of miR-26 host gene Ctdsp. Our study suggests that miR-26, its target Emx2 and its host gene Ctdsp cohesively regulate proliferation of NPs during the mouse cortical development.
引用
收藏
页数:12
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