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Engrailed-2突变小鼠中的模式畸形和细胞丢失表明在小脑发育过程中有两个独立的模式形成事件。

Pattern deformities and cell loss in Engrailed-2 mutant mice suggest two separate patterning events during cerebellar development.

作者信息

Kuemerle B, Zanjani H, Joyner A, Herrup K

机构信息

Alzheimer Research Laboratory, Case Western Reserve Medical School, Cleveland, Ohio 44106, USA.

出版信息

J Neurosci. 1997 Oct 15;17(20):7881-9. doi: 10.1523/JNEUROSCI.17-20-07881.1997.

Abstract

Null alleles of the mouse Engrailed-2 gene, a molecular homolog of the fly gene engrailed, have demonstrable effects on the anteroposterior (A/P) patterning of cerebellum as reflected in the disruption of the normal process of foliation of the cerebellar cortex and the alteration of transgene expression boundaries in the adult. Engrailed-2 also affects the transient mediolateral (M/L) pattern of En-1 and Wnt-7b expression seen in late embryogenesis. We have examined three markers of cerebellar compartmentation in En-2 mutant mice: the Zebrin II and Ppath monoclonal antibodies and the transgene L7lacZ. In En-2 mutants, the normal temporal pattern of expression is preserved for all three markers, although the size and spatial location of various bands differ from those of the wild type. Unlike the foliation abnormalities, the M/L pattern disturbances we have found occur in nearly all cerebellar regions. Cell counts reveal that all major cell types of the olivocerebellar circuit are reduced by 30-40%. We propose that these results are best explained by a model in which the Engrailed-2 gene is involved in the early specification of the cerebellar field including the number of progenitors. Because each of these progenitors gives rise to a clone of defined size, Engrailed-2 helps specify adult cell number. We further postulate that the configuration of the seven Zebrin bands as well as the shapes and locations of the cerebellar lobules are set up by a second patterning event that occurs after neurogenesis is complete.

摘要

小鼠Engrailed-2基因的无效等位基因是果蝇engrailed基因的分子同源物,对小脑的前后(A/P)模式形成有明显影响,这体现在小脑皮质正常叶状化过程的破坏以及成年期转基因表达边界的改变上。Engrailed-2还影响胚胎后期出现的En-1和Wnt-7b表达的短暂中外侧(M/L)模式。我们在En-2突变小鼠中检测了小脑分区的三个标志物:Zebrin II和Ppath单克隆抗体以及转基因L7lacZ。在En-2突变体中,所有三个标志物的正常表达时间模式得以保留,尽管不同条带的大小和空间位置与野生型不同。与叶状化异常不同,我们发现的M/L模式紊乱几乎发生在所有小脑区域。细胞计数显示,橄榄小脑回路的所有主要细胞类型减少了30-40%。我们认为,这些结果最好用一个模型来解释,即Engrailed-2基因参与了小脑区域的早期特化,包括祖细胞的数量。因为这些祖细胞中的每一个都会产生一个确定大小的克隆,所以Engrailed-2有助于确定成年细胞的数量。我们进一步推测,七条Zebrin带的构型以及小脑小叶的形状和位置是由神经发生完成后发生的第二个模式形成事件所建立的。

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