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Fgf8、Foxi1、Dlx3b和Pax8/2在青鳉耳泡诱导和维持过程中的不同作用。

Distinct roles of Fgf8, Foxi1, Dlx3b and Pax8/2 during otic vesicle induction and maintenance in medaka.

作者信息

Aghaallaei Narges, Bajoghli Baubak, Czerny Thomas

机构信息

Institute of Animal Breeding and Genetics, University of Veterinary Medicine, Veterinärplatz 1, A-1210 Vienna, Austria.

出版信息

Dev Biol. 2007 Jul 15;307(2):408-20. doi: 10.1016/j.ydbio.2007.04.022. Epub 2007 Apr 24.

Abstract

The development of the vertebrate inner ear is a complex process that has been investigated in several model organisms. In this work, we examined genetic interactions regulating early development of otic structures in medaka. We demonstrate that misexpression of Fgf8, Dlx3b and Foxi1 during early gastrulation is sufficient to produce ectopic otic vesicles. Combined misexpression strongly increases the appearance of this phenotype. By using a heat-inducible promoter we were furthermore able to separate the regulatory interactions among Fgf8, Foxi1, Dlx3b, Pax8 and Pax2 genes, which are active during different stages of early otic development. In the preplacodal stage we suggest a central position of Foxi1 within a regulatory network of early patterning genes including Dlx3b and Pax8. Different pathways are active after the placodal stage with Dlx3b playing a central role. There Dlx3b regulates members of the Pax-Six-Eya-Dach network and also strongly affects the early dorsoventral marker genes Otx1 and Gbx2.

摘要

脊椎动物内耳的发育是一个复杂的过程,已在多种模式生物中进行了研究。在这项工作中,我们研究了调控青鳉耳结构早期发育的基因相互作用。我们证明,在原肠胚形成早期阶段Fgf8、Dlx3b和Foxi1的错误表达足以产生异位耳泡。联合错误表达会强烈增加这种表型的出现。通过使用热诱导启动子,我们还能够区分Fgf8、Foxi1、Dlx3b、Pax8和Pax2基因之间的调控相互作用,这些基因在耳早期发育的不同阶段发挥作用。在基板前阶段,我们认为Foxi1在包括Dlx3b和Pax8在内的早期模式形成基因调控网络中处于中心位置。在基板阶段之后,不同的信号通路开始活跃,其中Dlx3b发挥核心作用。在那里,Dlx3b调控Pax-Six-Eya-Dach网络的成员,并且还强烈影响早期背腹标记基因Otx1和Gbx2。

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