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Hox基因通过秀丽隐杆线虫中的后部诱导促进神经元亚型多样化。

Hox Genes Promote Neuronal Subtype Diversification through Posterior Induction in Caenorhabditis elegans.

作者信息

Zheng Chaogu, Diaz-Cuadros Margarete, Chalfie Martin

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

Neuron. 2015 Nov 4;88(3):514-27. doi: 10.1016/j.neuron.2015.09.049.

Abstract

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.

摘要

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。

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