Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
EMBO J. 2012 Sep 12;31(18):3718-29. doi: 10.1038/emboj.2012.228. Epub 2012 Aug 17.
The formation of functional connectivity in the nervous system is governed by axon guidance that instructs nerve growth and branching during development, implying a similarity between neuronal subtypes in terms of nerve extension. We demonstrate the molecular mechanism of another layer of complexity in vertebrates by defining a transcriptional program underlying growth differences between positionally different neurons. The rate of axon extension of the early subset of embryonic dorsal root ganglion sensory neurons is encoded in neurons at different axial levels. This code is determined by a segmental pattern of axial levels of Runx family transcription factor Runx3. Runx3 in turn determines transcription levels of genes encoding cytoskeletal proteins involved in axon extension, including Rock1 and Rock2 which have ongoing activities determining axon growth in early sensory neurons and blocking Rock activity reverses axon extension deficits of Runx3(-/-) neurons. Thus, Runx3 acts to regulate positional differences in axon extension properties apparently without affecting nerve guidance and branching, a principle that could be relevant to other parts of the nervous system.
神经系统中功能连接的形成受轴突导向的控制,该导向在发育过程中指导神经生长和分支,这意味着神经元亚型在神经延伸方面具有相似性。我们通过定义位置不同神经元之间生长差异的转录程序,证明了脊椎动物中另一层复杂性的分子机制。早期胚胎背根神经节感觉神经元亚群的轴突延伸速度在不同轴向水平的神经元中被编码。这个代码是由 Runx 家族转录因子 Runx3 的节段性轴向水平模式决定的。Runx3 反过来又决定了参与轴突延伸的细胞骨架蛋白的基因转录水平,包括 Rock1 和 Rock2,它们在早期感觉神经元中持续活动决定轴突生长,并阻断 Rock 活性可逆转 Runx3(-/-)神经元的轴突延伸缺陷。因此,Runx3 似乎在不影响神经导向和分支的情况下调节轴突延伸特性的位置差异,这一原则可能与神经系统的其他部分有关。