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排斥性导向分子(RGM)基因功能对于小鼠视觉系统中的神经管闭合是必需的,但对于视网膜拓扑结构则不是必需的。

Repulsive guidance molecule (RGM) gene function is required for neural tube closure but not retinal topography in the mouse visual system.

作者信息

Niederkofler Vera, Salie Rishard, Sigrist Markus, Arber Silvia

机构信息

Biozentrum, Department of Cell Biology, University of Basel, 4056 Basel, Switzerland

出版信息

J Neurosci. 2004 Jan 28;24(4):808-18. doi: 10.1523/JNEUROSCI.4610-03.2004.

Abstract

The establishment of topographic projections in the developing visual system depends on the spatially and temporally controlled expression of axon guidance molecules. In the developing chick tectum, the graded expression of the repulsive guidance molecule (RGM) has been proposed to be involved in controlling the topography of the retinal ganglion cell (RGC) axon termination zones along the anteroposterior axis of the tectum. We now show that there are three mouse proteins homologous to chick RGM displaying similar proteolytic processing but exhibiting differential cell-surface targeting by glycosyl phosphatidylinositol anchor addition. Two members of this gene family (mRGMa and mRGMb) are expressed in complementary patterns in the nervous system, and mRGMa is expressed prominently in the superior colliculus at the time of anteroposterior targeting of RGC axons. The third member of the family (mRGMc) is expressed almost exclusively in skeletal muscles. Functional studies in the mouse reveal a role for mRGMa in controlling cephalic neural tube closure, thus defining an unexpected role for mRGMa in early embryonic development. In contrast, mRGMa mutant mice did not exhibit defects in anteroposterior targeting of RGC axons to their stereotypic termination zones in the superior colliculus.

摘要

发育中的视觉系统中地形投影的建立取决于轴突导向分子在空间和时间上的受控表达。在发育中的鸡视顶盖中,排斥性导向分子(RGM)的梯度表达被认为参与控制视网膜神经节细胞(RGC)轴突终止区沿视顶盖前后轴的地形。我们现在表明,有三种与鸡RGM同源的小鼠蛋白,它们显示出相似的蛋白水解加工,但通过添加糖基磷脂酰肌醇锚定表现出不同的细胞表面靶向。这个基因家族的两个成员(mRGMa和mRGMb)在神经系统中以互补模式表达,并且mRGMa在RGC轴突前后靶向时在上丘中显著表达。该家族的第三个成员(mRGMc)几乎只在骨骼肌中表达。对小鼠的功能研究揭示了mRGMa在控制头部神经管闭合中的作用,从而确定了mRGMa在早期胚胎发育中的一个意想不到的作用。相比之下,mRGMa突变小鼠在RGC轴突向上丘中其刻板终止区的前后靶向中没有表现出缺陷。

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