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Gli3对于端脑背侧发育过程中Emx基因的表达是必需的。

Gli3 is required for Emx gene expression during dorsal telencephalon development.

作者信息

Theil T, Alvarez-Bolado G, Walter A, Rüther U

机构信息

Institute for Molecular Biology, Hannover Medical School, Carl-Neuberg-Strasse 1, D-30625 Hannover, Germany. thomas.

出版信息

Development. 1999 Aug;126(16):3561-71. doi: 10.1242/dev.126.16.3561.

Abstract

Dentate gyrus and hippocampus as centers for spatial learning, memory and emotional behaviour have been the focus of much interest in recent years. The molecular information on its development, however, has been relatively poor. To date, only Emx genes were known to be required for dorsal telencephalon development. Here, we report on forebrain development in the extra toes (Xt(J)) mouse mutant which carries a null mutation of the Gli3 gene. This defect leads to a failure to establish the dorsal di-telencephalic junction and finally results in a severe size reduction of the neocortex. In addition, Xt(J)/Xt(J) mice show absence of the hippocampus (Ammon's horn plus dentate gyrus) and the choroid plexus in the lateral ventricle. The medial wall of the telencephalon, which gives rise to these structures, fails to invaginate during embryonic development. On a molecular level, disruption of dorsal telencephalon development in Xt(J)/Xt(J) embryos correlates with a loss of Emx1 and Emx2 expression. Furthermore, the expression of Fgf8 and Bmp4 in the dorsal midline of the telencephalon is altered. However, expression of Shh, which is negatively regulated by Gli3 in the spinal cord, is not affected in the Xt(J)/Xt(J) forebrain. This study therefore implicates Gli3 as a key regulator for the development of the dorsal telencephalon and implies Gli3 to be upstream of Emx genes in a genetic cascade controlling dorsal telencephalic development.

摘要

齿状回和海马体作为空间学习、记忆及情绪行为的中心,近年来备受关注。然而,关于其发育的分子信息相对较少。迄今为止,已知只有Emx基因是背侧端脑发育所必需的。在此,我们报道携带Gli3基因无效突变的extra toes(Xt(J))小鼠突变体的前脑发育情况。这种缺陷导致背侧间脑连接处无法形成,最终导致新皮层严重缩小。此外,Xt(J)/Xt(J)小鼠的海马体(海马角加齿状回)和侧脑室脉络丛缺失。产生这些结构的端脑内侧壁在胚胎发育过程中未能内陷。在分子水平上,Xt(J)/Xt(J)胚胎中背侧端脑发育的破坏与Emx1和Emx2表达的丧失相关。此外,端脑背侧中线处Fgf8和Bmp4的表达发生改变。然而,在脊髓中受Gli3负调控的Shh在Xt(J)/Xt(J)前脑中的表达未受影响。因此,本研究表明Gli3是背侧端脑发育的关键调节因子,并暗示Gli3在控制背侧端脑发育的基因级联反应中位于Emx基因的上游。

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