Feedback regulation of NEUROG2 activity by MTGR1 is required for progression of neurogenesis

被引:11
作者
Aaker, Joshua D.
Patineau, Andrea L.
Yang, Hyun-jin
Ewart, David T.
Gong, Wuming
Li, Tongbin
Nakagawa, Yasushi
McLoon, Steven C.
Koyano-Nakagawa, Naoko [1 ]
机构
[1] Univ Minnesota, Dept Neurosci, Minneapolis, MN 55455 USA
关键词
Development; Neurogenesis; Embryo; Transcription; bHLH; Spinal cord; MTGR1; NEUROG2; MTG/ETO proteins; Nervy; Transcriptional repressor; BHLH TRANSCRIPTION FACTORS; CELL FATE SPECIFICATION; GLIAL DIFFERENTIATION; PYRAMIDAL NEURONS; PRONEURAL BHLH; DEVELOPING CNS; EXPRESSION; PROTEIN; PROMOTES; GENES;
D O I
10.1016/j.mcn.2009.07.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The sequential steps of neurogenesis are characterized by highly choreographed changes in transcription factor activity. in contrast to the well-studied mechanisms of transcription factor activation during neurogenesis, much less is understood regarding how such activity is terminated. We previously showed that MTGR1, a member of the MTG family of transcriptional repressors, is strongly induced by a proneural basic helix-loop-helix transcription factor, NEUROG2 in developing nervous system. In this study, we describe a novel feedback regulation of NEUROG2 activity by MTGR1. We show that MTGR1 physically interacts with NEUROG2 and represses transcriptional activity of NEUROG2. MTGR1 also prevents DNA binding of the NEUROG2/E47 complex. In addition, we provide evidence that proper termination of NEUROG2 activity by MTGR1 is necessary for normal progression of neurogenesis in the developing spinal cord. These results highlight the importance of feedback regulation of proneural gene activity in neurodevelopment. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:267 / 277
页数:11
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