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翻译抑制决定了果蝇不对称细胞分裂中的神经元潜能。

Translational repression determines a neuronal potential in Drosophila asymmetric cell division.

作者信息

Okabe M, Imai T, Kurusu M, Hiromi Y, Okano H

机构信息

Division of Developmental Genetics, National Institute of Genetics, and Department of Genetics, Graduate University for Advanced Studies, 1111 Yata, Mishima, Shizuoka 411-8540, Japan.

出版信息

Nature. 2001 May 3;411(6833):94-8. doi: 10.1038/35075094.

Abstract

Asymmetric cell division is a fundamental strategy for generating cellular diversity during animal development. Daughter cells manifest asymmetry in their differential gene expression. Transcriptional regulation of this process has been the focus of many studies, whereas cell-type-specific 'translational' regulation has been considered to have a more minor role. During sensory organ development in Drosophila, Notch signalling directs the asymmetry between neuronal and non-neuronal lineages, and a zinc-finger transcriptional repressor Tramtrack69 (TTK69) acts downstream of Notch as a determinant of non-neuronal identity. Here we show that repression of TTK69 protein expression in the neuronal lineage occurs translationally rather than transcriptionally. This translational repression is achieved by a direct interaction between cis-acting sequences in the 3' untranslated region of ttk69 messenger RNA and its trans-acting repressor, the RNA-binding protein Musashi (MSI). Although msi can act downstream of Notch, Notch signalling does not affect MSI expression. Thus, Notch signalling is likely to regulate MSI activity rather than its expression. Our results define cell-type-specific translational control of ttk69 by MSI as a downstream event of Notch signalling in asymmetric cell division.

摘要

不对称细胞分裂是动物发育过程中产生细胞多样性的一种基本策略。子细胞在其差异基因表达中表现出不对称性。这一过程的转录调控一直是许多研究的重点,而细胞类型特异性的“翻译”调控则被认为作用较小。在果蝇感觉器官发育过程中,Notch信号传导指导神经元和非神经元谱系之间的不对称性,锌指转录抑制因子Tramtrack69(TTK69)作为非神经元身份的决定因素,在Notch信号下游发挥作用。我们在此表明,神经元谱系中TTK69蛋白表达的抑制发生在翻译水平而非转录水平。这种翻译抑制是通过ttk69信使核糖核酸3'非翻译区中的顺式作用序列与其反式作用抑制因子——RNA结合蛋白Musashi(MSI)之间的直接相互作用实现的。尽管msi可以在Notch信号下游发挥作用,但Notch信号传导并不影响MSI的表达。因此,Notch信号传导可能调节MSI的活性而非其表达。我们的研究结果将MSI对ttk69的细胞类型特异性翻译控制定义为不对称细胞分裂中Notch信号传导的下游事件。

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