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Tbx1对神经命运的抑制及内耳形态发生的调控

Suppression of neural fate and control of inner ear morphogenesis by Tbx1.

作者信息

Raft Steven, Nowotschin Sonja, Liao Jun, Morrow Bernice E

机构信息

Department of Neuroscience, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

出版信息

Development. 2004 Apr;131(8):1801-12. doi: 10.1242/dev.01067. Epub 2004 Mar 17.

Abstract

Inner ear sensory organs and VIIIth cranial ganglion neurons of the auditory/vestibular pathway derive from an ectodermal placode that invaginates to form an otocyst. We show that in the mouse otocyst epithelium, Tbx1 suppresses neurogenin 1-mediated neural fate determination and is required for induction or proper patterning of gene expression related to sensory organ morphogenesis (Otx1 and Bmp4, respectively). Tbx1 loss-of-function causes dysregulation of neural competence in otocyst regions linked to the formation of either mechanosensory or structural sensory organ epithelia. Subsequently, VIIIth ganglion rudiment form is duplicated posteriorly, while the inner ear is hypoplastic and shows neither a vestibular apparatus nor a coiled cochlear duct. We propose that Tbx1 acts in the manner of a selector gene to control neural and sensory organ fate specification in the otocyst.

摘要

听觉/前庭通路的内耳感觉器官和第八脑神经节神经元起源于一个内陷形成耳囊的外胚层基板。我们发现,在小鼠耳囊上皮中,Tbx1抑制神经生成素1介导的神经命运决定,并且是诱导或正确形成与感觉器官形态发生相关的基因表达(分别为Otx1和Bmp4)所必需的。Tbx1功能丧失导致与机械感觉或结构感觉器官上皮形成相关的耳囊区域神经能力失调。随后,第八神经节原基在后方重复形成,而内耳发育不全,既没有前庭装置也没有卷曲的耳蜗管。我们提出,Tbx1以选择基因的方式发挥作用,以控制耳囊中神经和感觉器官命运的特化。

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