Zheng Chaogu, Diaz-Cuadros Margarete, Chalfie Martin
Department of Biological Sciences, Columbia University, New York, NY 10027, USA.
Department of Biological Sciences, Columbia University, New York, NY 10027, USA.
Neuron. 2015 Nov 4;88(3):514-27. doi: 10.1016/j.neuron.2015.09.049.
Although Hox genes specify the differentiation of neuronal subtypes along the anterior-posterior axis, their mode of action is not entirely understood. Using two subtypes of the touch receptor neurons (TRNs) in C. elegans, we found that a "posterior induction" mechanism underlies the Hox control of terminal neuronal differentiation. The anterior subtype maintains a default TRN state, whereas the posterior subtype undergoes further morphological and transcriptional specification induced by the posterior Hox proteins, mainly EGL-5/Abd-B. Misexpression of the posterior Hox proteins transformed the anterior TRN subtype toward a posterior identity both morphologically and genetically. The specification of the posterior subtype requires EGL-5-induced repression of TALE cofactors, which antagonize EGL-5 functions, and the activation of rfip-1, a component of recycling endosomes, which mediates Hox activities by promoting subtype-specific neurite outgrowth. Finally, EGL-5 is required for subtype-specific circuit formation by acting in both the sensory neuron and downstream interneuron to promote functional connectivity.
尽管Hox基因决定了沿前后轴的神经元亚型的分化,但其作用方式尚未完全明确。利用秀丽隐杆线虫中的两种触觉感受器神经元(TRN)亚型,我们发现一种“后部诱导”机制是Hox对终末神经元分化进行控制的基础。前部亚型维持默认的TRN状态,而后部亚型则经历由后部Hox蛋白(主要是EGL-5/Abd-B)诱导的进一步形态和转录特化。后部Hox蛋白的错误表达在形态和遗传上都将前部TRN亚型转变为后部特征。后部亚型的特化需要EGL-5诱导对TALE辅因子的抑制,TALE辅因子会拮抗EGL-5的功能,以及rfip-1的激活,rfip-1是循环内体的一个组分,它通过促进亚型特异性神经突生长来介导Hox活性。最后,EGL-5通过在感觉神经元和下游中间神经元中发挥作用以促进功能连接,从而参与亚型特异性神经回路的形成。