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神经前体蛋白的负反馈调节控制神经前体分裂的时间。

Negative-feedback regulation of proneural proteins controls the timing of neural precursor division.

作者信息

Chang Pao-Ju, Hsiao Yun-Ling, Tien An-Chi, Li Yi-Chen, Pi Haiwei

机构信息

Department of Life Science, Chang-Gung University, 259 Wen-Hwa 1st Road, Kwei-Shan, Tao-Yuan 333, Taiwan.

出版信息

Development. 2008 Sep;135(18):3021-30. doi: 10.1242/dev.021923. Epub 2008 Aug 13.

DOI:10.1242/dev.021923
PMID:18701547
Abstract

Neurogenesis requires precise control of cell specification and division. In Drosophila, the timing of cell division of the sensory organ precursor (SOP) is under strict temporal control. But how the timing of mitotic entry is determined remains poorly understood. Here, we present evidence that the timing of the G2-M transition is determined by when proneural proteins are degraded from SOPs. This process requires the E3 ubiquitin ligase complex, including the RING protein Sina and the adaptor Phyl. In phyl mutants, proneural proteins accumulate, causing delay or arrest in the G2-M transition. The G2-M defect in phyl mutants is rescued by reducing the ac and sc gene doses. Misexpression of phyl downregulates proneural protein levels in a sina-dependent manner. Phyl directly associates with proneural proteins to act as a bridge between proneural proteins and Sina. As phyl is a direct transcriptional target of Ac and Sc, our data suggest that, in addition to mediating cell cycle arrest, proneural protein initiates a negative-feedback regulation to time the mitotic entry of neural precursors.

摘要

神经发生需要对细胞特化和分裂进行精确控制。在果蝇中,感觉器官前体细胞(SOP)的细胞分裂时间受到严格的时间控制。但是,有丝分裂进入的时间是如何确定的,目前仍知之甚少。在这里,我们提供证据表明,G2-M转换的时间是由神经前体蛋白从SOP中降解的时间决定的。这个过程需要E3泛素连接酶复合物,包括环状蛋白Sina和衔接蛋白Phyl。在phyl突变体中,神经前体蛋白积累,导致G2-M转换延迟或停滞。通过降低ac和sc基因剂量,可以挽救phyl突变体中的G2-M缺陷。phyl的错误表达以sina依赖的方式下调神经前体蛋白水平。Phyl直接与神经前体蛋白结合,作为神经前体蛋白和Sina之间的桥梁。由于phyl是Ac和Sc的直接转录靶点,我们的数据表明,除了介导细胞周期停滞外,神经前体蛋白还启动了一种负反馈调节,以确定神经前体细胞有丝分裂进入的时间。

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