早期中脑/后脑模式和小脑的发育。

M Wassef, A L Joyner
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引用次数: 0

摘要

雏鸡的实验研究和小鼠突变体的分析为研究小脑样本的早期发育过程提供了一个框架。小鸡的命运图谱研究表明,在早期阶段,小脑来源于中脑和后脑(mesencephalon)的细胞。鸡的移植研究表明,接合处(峡部)是组织整个接合处发育的分泌因子的来源,可能是通过刺激增殖和指定整个区域的位置值。Fgf-8被认为是参与峡部组织活动的一个主要因素。基因表达研究表明,同源盒基因Otx-2和Gbx-2的前、后表达域分别是大脑分裂的最早迹象。此外,Otx-2/Gbx-2的表达边界随后位于mes-met交界处。小鼠的遗传研究表明,Otx-2和Gbx-2是边界两侧细胞正常发育所必需的。此外,影响分泌因子Wnt-1(在Otx-2/Gbx-2表达边界前表达)和同源域转录因子engrailed -1,2和pax -2,5(在mes-met中具有广泛重叠表达域)的突变会导致mes-met结构的缺失。综上所述,这些研究表明,小脑区域的指定需要复杂的细胞和基因相互作用的层次结构,这些相互作用逐渐将大脑细分为更小的区域。
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Early mesencephalon/metencephalon patterning and development of the cerebellum.

Experimental studies in chick and analysis of mouse mutants have provided a framework for studying the early developmental processes involved in specifying the cerebellar anlage. Fate mapping studies in chick have shown that at early stages the cerebellum derives from cells in the mesencephalon and metencephalon (mes-met). Transplantation studies in chick have implicated the mes-met junction (isthmus) as a source of secreted factors that organize development of the entire mes-met, perhaps by stimulating proliferation and specifying positional values across the region. Fgf-8 has been implicated as a major factor involved in the isthmus organizing activity. Gene expression studies indicate that the anterior and posterior expression domains of the homeobox genes Otx-2 and Gbx-2, respectively, are the earliest indication of a division of the brain. Furthermore, the Otx-2/Gbx-2 expression border later resides at the mes-met junction. Genetic studies in mouse have shown that Otx-2 and Gbx-2 are required for normal development of cells on both sides of the border. In addition, mutations affecting the secreted factor Wnt-1, which is expressed anterior to the Otx-2/Gbx-2 expression border and the homeodomain transcription factors, Engrailed-1,2 and Pax-2,5 that have broad overlapping expression domains in the mes-met, result in deletions of mes-met structures. Taken together, these studies suggest that specification of the cerebellar territory requires a hierarchy of complex cellular and genetic interactions that gradually subdivide the brain into smaller regions.

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