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音猬因子(Shh)通过激活斑马鱼视网膜中的p57Kip2来引导细胞周期退出。

Shh directs cell-cycle exit by activating p57Kip2 in the zebrafish retina.

作者信息

Shkumatava Alena, Neumann Carl J

机构信息

EMBL Heidelberg, Meyerhofstrasse 1, 69117 Heidelberg, Germany.

出版信息

EMBO Rep. 2005 Jun;6(6):563-9. doi: 10.1038/sj.embor.7400416.

Abstract

The Hedgehog (Hh) family of signalling proteins control both differentiation and proliferation during animal development. Previous studies have shown that Hh signalling has a stimulatory effect on the cell cycle in several organs by controlling core cell-cycle components. Here, we show that Sonic hedgehog (Shh) signalling has the opposite effect in the zebrafish retina, where it leads to cell-cycle exit, and that this is mediated by transcriptional activation of the cyclin kinase inhibitor p57Kip2. The loss of p57Kip2 activity strongly resembles the Shh mutant eye phenotype, and overexpression of p57Kip2 rescues cell-cycle exit in Shh mutants, indicating that p57Kip2 is both necessary and sufficient to mediate Shh-induced cell-cycle exit in the retina. These findings raise the possibility that stimulation of cell-cycle exit through regulation of core cell-cycle components may be part of a general mechanism required for Hh-directed differentiation.

摘要

刺猬信号蛋白家族(Hh)在动物发育过程中控制细胞分化和增殖。先前的研究表明,Hh信号通过控制核心细胞周期成分对多个器官的细胞周期有刺激作用。在此,我们表明,音猬因子(Shh)信号在斑马鱼视网膜中具有相反的作用,它导致细胞周期退出,并且这是由细胞周期蛋白激酶抑制剂p57Kip2的转录激活介导的。p57Kip2活性的丧失与Shh突变体的眼部表型非常相似,并且p57Kip2的过表达挽救了Shh突变体中的细胞周期退出,表明p57Kip2对于介导视网膜中Shh诱导的细胞周期退出既是必需的也是充分的。这些发现增加了一种可能性,即通过调节核心细胞周期成分来刺激细胞周期退出可能是Hh定向分化所需的一般机制的一部分。

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