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Regulation and function of FGF8 in patterning of midbrain and anterior hindbrain

机译:FGF8在中脑和后脑模式中的调控及其功能

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In this article, an adjunct to a platform presentation at the Winternational 2000 Symposium, we summarize the recent findings of this group concerning the regulation and functions of FGF8 expressed at the isthmus of the Warn ell- veloping brain. We show that several different FGF8 isoforms, ectopically expressed in midbrain or posterior forebrain, are able to mimic the proliferative and patterning functions previously attributed to the isthmus in tissue grafting studies. Moreover, we also show that FGF8 protein is sufficient to induce an ectopic isthmic organiser (Fgf-8+, Gbx2+) in anterior midbrain. We also provide' evidence that isthmic FGF8 patterns anterior hindbrain, repressing Hox-a2 expression and setting aside a territory of the brain that includes the cerebellar anlage. We show that these effects of FGF8 are likely to be mediated via FGFR1 and be modulated by the putative FGF antagonist, Sprouty2, identified using a differential display screen. Finally, we provide evidence that the onset of Fgf8 expression is regulated by Enl and that its expression at the isthmus is subsequently maintained by a specific and direct interaction between rhombomere 1 and midbrain.
机译:在本文中,作为2000年Winternational研讨会平台演讲的辅助,我们总结了该小组有关在Warn大脑峡部表达的FGF8的调控和功能的最新发现。我们显示几种不同的FGF8亚型,异位表达在中脑或前脑后部,能够模仿先前在组织移植研究中峡部的增殖和模式功能。此外,我们还表明FGF8蛋白足以诱导中脑前部的异位缺血组织者(Fgf-8 +,Gbx2 +)。我们还提供了证据,即峡部FGF8会图案化后后脑,抑制Hox-a2表达并预留包括小脑territory突在内的大脑区域。我们显示,FGF8的这些作用很可能是通过FGFR1介导的,并被公认的FGF拮抗剂Sprouty2调节,使用差异显示屏幕进行了鉴定。最后,我们提供证据表明Fgf8表达的发作受Enl调节,并且其在峡部的表达随后通过菱形1和中脑之间的特异性直接相互作用得以维持。

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