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Par-1通过磷酸化Exuperantia来调节双胸节mRNA的定位。

Par-1 regulates bicoid mRNA localisation by phosphorylating Exuperantia.

作者信息

Riechmann Veit, Ephrussi Anne

机构信息

European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany.

出版信息

Development. 2004 Dec;131(23):5897-907. doi: 10.1242/dev.01515.

Abstract

The Ser/Thr kinase Par-1 is required for cell polarisation in diverse organisms such as yeast, worms, flies and mammals. During Drosophila oogenesis, Par-1 is required for several polarisation events, including localisation of the anterior determinant bicoid. To elucidate the molecular pathways triggered by Par-1, we have performed a genome-wide, high-throughput screen for Par-1 targets. Among the targets identified in this screen was Exuperantia (Exu), a mediator of bicoid mRNA localisation. We show that Exu is a phosphoprotein whose phosphorylation is dependent on Par-1 in vitro and in vivo. We identify two motifs in Exu that are phosphorylated by Par-1, and show that their mutation abolishes bicoid mRNA localisation during mid-oogenesis. Interestingly, exu mutants in which Exu phosphorylation is specifically affected can to some extent recover from these bicoid mRNA localisation defects during late oogenesis. These results demonstrate that Par-1 establishes polarity in the oocyte by activating a mediator of bicoid mRNA localisation. Furthermore, our analysis reveals two phases of Exu-dependent bicoid mRNA localisation: an early phase that is strictly dependent on Exu phosphorylation and a late phase that is less phosphorylation dependent.

摘要

丝氨酸/苏氨酸激酶Par-1在多种生物(如酵母、线虫、果蝇和哺乳动物)的细胞极化过程中是必需的。在果蝇卵子发生过程中,Par-1参与多个极化事件,包括前体决定因子双尾蛋白的定位。为了阐明由Par-1触发的分子途径,我们进行了全基因组的高通量筛选以寻找Par-1的靶标。在该筛选中鉴定出的靶标之一是Exuperantia(Exu),它是双尾蛋白mRNA定位的介导因子。我们发现Exu是一种磷酸化蛋白,其磷酸化在体外和体内均依赖于Par-1。我们在Exu中鉴定出两个被Par-1磷酸化的基序,并表明它们的突变会消除卵子发生中期双尾蛋白mRNA的定位。有趣的是,Exu磷酸化受到特异性影响的exu突变体在卵子发生后期可以在一定程度上从这些双尾蛋白mRNA定位缺陷中恢复。这些结果表明,Par-1通过激活双尾蛋白mRNA定位的介导因子在卵母细胞中建立极性。此外,我们的分析揭示了依赖Exu的双尾蛋白mRNA定位的两个阶段:一个早期阶段严格依赖于Exu磷酸化,一个后期阶段对磷酸化的依赖性较小。

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