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An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism

机译:一个指间信号中心指示受5Hoxd-Gli3拮抗作用控制的指骨节关节形成

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摘要

The number of phalanges and joints are key features of digit ‘identity' and are central to limb functionality and evolutionary adaptation. Prior chick work indicated that digit phalanges and their associated joints arise in a different manner than the more sparsely jointed long bones, and their identity is regulated by differential signalling from adjacent interdigits. Currently, there is no genetic evidence for this model, and the molecular mechanisms governing digit joint specification remain poorly understood. Using genetic approaches in mouse, here we show that functional 5′Hoxd–Gli3 antagonism acts indirectly, through Bmp signalling from the interdigital mesenchyme, to regulate specification of joint progenitors, which arise in conjunction with phalangeal precursors at the digit tip. Phalanx number, although co-regulated, can be uncoupled from joint specification. We propose that 5′Hoxd genes and Gli3 are part of an interdigital signalling centre that sets net Bmp signalling levels from different interdigits to coordinately regulate phalanx and joint formation.
机译:指骨和关节的数量是数字“身份”的关键特征,对于肢体功能和进化适应至关重要。先前的雏鸡研究表明,指骨趾骨及其相关的关节以与稀疏连接的长骨不同的方式出现,并且它们的身份受到相邻指间的差异信号的调节。目前,尚无此模型的遗传学证据,控制手指关节规格的分子机制仍知之甚少。使用小鼠的遗传学方法,在这里我们显示功能性5'Hoxd–Gli3拮抗作用是通过指间间充质的Bmp信号间接作用来调节关节祖细胞的规格,后者与指趾前体在指尖结合出现。尽管方阵数是共同调节的,但可以与联合规范脱钩。我们建议5'Hoxd基因和Gli3是一个叉指信号中心的一部分,该中心设置来自不同叉指的净Bmp信号水平来协调调节趾骨和关节的形成。

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