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Gli3的一种不依赖于音猬因子(SHH)的调控是肢芽前后模式形成的一个重要决定因素。

A SHH-independent regulation of Gli3 is a significant determinant of anteroposterior patterning of the limb bud.

作者信息

Hill Patrick, Götz Katrin, Rüther Ulrich

机构信息

Institut für Entwicklungs- und Molekularbiologie der Tiere, Heinrich-Heine-Universität Düsseldorf, 40225 Düsseldorf, Germany.

出版信息

Dev Biol. 2009 Apr 15;328(2):506-16. doi: 10.1016/j.ydbio.2009.02.017. Epub 2009 Feb 24.

Abstract

The family of GLI proteins (GLI1-3) comprises the intracellular mediators of the hedgehog pathway, which regulates a myriad of developmental processes, one of which is limb development. Whereas GLI1 and GLI2 seem to be dispensable during limb development, GLI3 is especially crucial since all GLI3-associated human congenital diseases comprise limb malformations. Furthermore, Gli3(-/-) mouse embryos exhibit pronounced polydactyly in conjunction with a loss of digit identities. Here we examined how the quantity of GLI3 contributes to its function by using different Gli3 mutants in order to vary overall GLI3 levels. In addition, we made use of the Gli3(Delta699) allele, which encodes a C-terminally truncated version of GLI3, thus mimicking the processed GLI3 isoform (GLI3R). The Gli3(Delta699) mutant made it feasible to analyze isoform-specific contributions of GLI3 within the context of anteroposterior patterning of the limb bud. We revealed a so far unappreciated variation in the quantitative demand for GLI3 within different phases and aspects of distal limb formation. In addition, our analyses provide evidence that unprocessed full-length GLI3 is dispensable for anteroposterior patterning of the limb bud. Instead, digit identities are most likely defined by GLI3 repressor activity alone. Furthermore, we present evidence that the anteroposterior grading of GLI3 activity by the action of SHH is supported by a prototype patterning, which regulates Gli3 independently from SHH.

摘要

GLI蛋白家族(GLI1 - 3)是刺猬信号通路的细胞内介质,该通路调节众多发育过程,其中之一是肢体发育。虽然GLI1和GLI2在肢体发育过程中似乎并非必需,但GLI3尤为关键,因为所有与GLI3相关的人类先天性疾病都包含肢体畸形。此外,Gli3(-/-)小鼠胚胎表现出明显的多指畸形,并伴有指身份的丧失。在这里,我们通过使用不同的Gli3突变体来改变总体GLI3水平,研究了GLI3的数量如何影响其功能。此外,我们利用了Gli3(Delta699)等位基因,它编码一种C末端截短的GLI3版本,从而模拟加工后的GLI3异构体(GLI3R)。Gli3(Delta699)突变体使我们能够在肢芽前后模式形成的背景下分析GLI3异构体特异性的作用。我们揭示了在远端肢体形成的不同阶段和方面,对GLI3的定量需求存在迄今未被认识到的差异。此外,我们的分析提供了证据,表明未加工的全长GLI3对于肢芽的前后模式形成并非必需。相反,指身份很可能仅由GLI3阻遏物活性来定义。此外,我们提供的证据表明,由SHH作用引起的GLI3活性的前后梯度是由一种原型模式支持的,该模式独立于SHH调节Gli3。

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