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Hox 基因网络在小鼠脑干中对听觉回路的组装。

Assembly of the auditory circuitry by a Hox genetic network in the mouse brainstem.

机构信息

Telethon Institute of Genetics and Medicine (TIGEM), Naples, Italy.

出版信息

PLoS Genet. 2013;9(2):e1003249. doi: 10.1371/journal.pgen.1003249. Epub 2013 Feb 7.

Abstract

Rhombomeres (r) contribute to brainstem auditory nuclei during development. Hox genes are determinants of rhombomere-derived fate and neuronal connectivity. Little is known about the contribution of individual rhombomeres and their associated Hox codes to auditory sensorimotor circuitry. Here, we show that r4 contributes to functionally linked sensory and motor components, including the ventral nucleus of lateral lemniscus, posterior ventral cochlear nuclei (VCN), and motor olivocochlear neurons. Assembly of the r4-derived auditory components is involved in sound perception and depends on regulatory interactions between Hoxb1 and Hoxb2. Indeed, in Hoxb1 and Hoxb2 mutant mice the transmission of low-level auditory stimuli is lost, resulting in hearing impairments. On the other hand, Hoxa2 regulates the Rig1 axon guidance receptor and controls contralateral projections from the anterior VCN to the medial nucleus of the trapezoid body, a circuit involved in sound localization. Thus, individual rhombomeres and their associated Hox codes control the assembly of distinct functionally segregated sub-circuits in the developing auditory brainstem.

摘要

神经管的菱形体(r)在发育过程中有助于脑干听觉核。Hox 基因是菱形体衍生命运和神经元连接的决定因素。关于单个菱形体及其相关 Hox 代码对听觉感觉运动回路的贡献知之甚少。在这里,我们表明 r4 有助于功能上相关的感觉和运动成分,包括外侧丘系腹核、后腹侧耳蜗核(VCN)和运动橄榄耳蜗神经元。r4 衍生的听觉成分的组装涉及声音感知,并取决于 Hoxb1 和 Hoxb2 之间的调节相互作用。事实上,在 Hoxb1 和 Hoxb2 突变小鼠中,低水平听觉刺激的传递丢失,导致听力受损。另一方面,Hoxa2 调节 Rig1 轴突导向受体,并控制来自前 VCN 到梯形体内侧核的对侧投射,这是一个参与声音定位的回路。因此,单个菱形体及其相关的 Hox 代码控制着发育中的听觉脑干中不同功能分离的亚回路的组装。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc41/3567144/96c06dba33c8/pgen.1003249.g001.jpg

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