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在脊椎动物肢体发育过程中,Pax9和Jagged1在Gli3的下游发挥作用。

Pax9 and Jagged1 act downstream of Gli3 in vertebrate limb development.

作者信息

McGlinn Edwina, van Bueren Kelly Lammerts, Fiorenza Salvatore, Mo Rong, Poh Alisa M, Forrest Alistair, Soares Marcelo Bento, Bonaldo Maria de Fatima, Grimmond Sean, Hui Chi-Chung, Wainwright Brandon, Wicking Carol

机构信息

Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld 4072, Australia.

出版信息

Mech Dev. 2005 Nov;122(11):1218-33. doi: 10.1016/j.mod.2005.06.012. Epub 2005 Aug 1.

Abstract

From early in limb development the transcription factor Gli3 acts to define boundaries of gene expression along the anterior-posterior (AP) axis, establishing asymmetric patterns required to provide positional information. As limb development proceeds, posterior mesenchyme expression of Sonic hedgehog (Shh) regulates Gli3 transcription and post-translational processing to specify digit number and identity. The molecular cascades dependent on Gli3 at later stages of limb development, which link early patterning events with final digit morphogenesis, remain poorly characterised. By analysing the transcriptional consequences of loss of Gli3 in the anterior margin of the E11.5 and E12.5 limb bud in the polydactylous mouse mutant extra-toes (Gli3(Xt/Xt)), we have identified a number of known and novel transcripts dependent on Gli3 in the limb. In particular, we demonstrated that the genes encoding the paired box transcription factor Pax9, the Notch ligand Jagged1 and the cell surface receptor Cdo are dependent on Gli3 for correct expression in the anterior limb mesenchyme. Analysis of expression in compound Shh;Gli3 mutant mouse embryos and in both in vitro and in vivo Shh signaling assays, further defined the importance of Shh regulated processing of Gli3 in controlling gene expression. In particular Pax9 regulation by Shh and Gli3 was shown to be context dependent, with major differences between the limb and somite revealed by Shh bead implantation experiments in the chick. Jagged1 was shown to be induced by Shh in the chick limb and in a C3H10T1/2 cell based signaling assay, with Shh;Gli3 mutant analysis indicating that expression is dependent on Gli3 derepression. Our data have also revealed that perturbation of early patterning events within the Gli3(Xt/Xt) limb culminates in a specific delay of anterior chondrogenesis which is subsequently realised as extra digits.

摘要

从肢体发育早期开始,转录因子Gli3就发挥作用,沿前后(AP)轴定义基因表达边界,建立提供位置信息所需的不对称模式。随着肢体发育的进行,音猬因子(Shh)在后侧间充质中的表达调节Gli3的转录和翻译后加工,以确定指(趾)的数量和特性。在肢体发育后期依赖Gli3的分子级联反应,将早期模式形成事件与最终的指(趾)形态发生联系起来,其特征仍不清楚。通过分析多指小鼠突变体extra-toes(Gli3(Xt/Xt))中E11.5和E12.5肢体芽前缘Gli3缺失的转录后果,我们确定了肢体中一些已知和新的依赖Gli3的转录本。特别是,我们证明了编码配对盒转录因子Pax9、Notch配体Jagged1和细胞表面受体Cdo的基因在前肢间充质中的正确表达依赖于Gli3。对复合Shh;Gli3突变小鼠胚胎以及体外和体内Shh信号转导试验中的表达分析,进一步确定了Shh调节Gli3加工在控制基因表达中的重要性。特别是,Shh和Gli3对Pax9的调节显示出依赖于背景,在鸡中通过Shh珠子植入实验揭示了肢体和体节之间的主要差异。Jagged1在鸡肢体和基于C3H10T1/2细胞的信号转导试验中被Shh诱导,对Shh;Gli3突变体的分析表明其表达依赖于Gli3的去抑制。我们的数据还表明,Gli3(Xt/Xt)肢体中早期模式形成事件的扰动最终导致前软骨形成的特定延迟,随后表现为多指。

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