Spatiotemporally restricted regulation of generic motor neuron programs by miR-196-mediated repression of Hoxb8

被引:43
作者
Asli, Naisana S. [1 ]
Kessel, Michael [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Mol Cell Biol, Res Grp Dev Biol, D-37077 Gottingen, Germany
关键词
MicroRNAs; Hox genes; Motor neuron generation; Cell cycle; CELL FATE SPECIFICATION; HOX-2.4 HOMEOBOX GENE; SPINAL-CORD; SUBTYPE IDENTITY; PROGENITOR CELLS; NERVOUS-SYSTEM; MESSENGER-RNA; MECHANISMS; EXPRESSION; MICRORNAS;
D O I
10.1016/j.ydbio.2010.06.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hox transcription factors are key determinants of antero-posterior identity and have been implicated in assigning positionally appropriate neuron subtypes in the neural tube. These roles inherently necessitate stringent control mechanisms that confine Hox protein activities to discrete spatiotemporal domains. Here, we provide evidence that the timing and rostro-caudal extent of Hoxb8 activity in the neural tube is tightly regulated by miR-196, a microRNA species encoded within three Hox gene clusters. In vitro and in vivo sensor-tracer analysis and transcription assays revealed that miR-196 activity restricts the caudal extent of Hoxb8 expression to the thoracic-lumbar intersect via 3' UTR-dependent negative regulation. Spatiotemporally inappropriate Hoxb8 activity, through relief of miR-196-mediated repression or direct misexpression, affected normal progression of motor neuron genesis by affecting generic motor neuron differentiation programs. In addition to uncovering a role for microRNA-dependent restriction of caudal Hox activities, these data thus indicate novel aspects of Hox-dependent neural tube patterning by revealing a requirement of temporal regulation of a generic neuronal specification program. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:857 / 868
页数:12
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