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Lgl及其被非典型蛋白激酶C磷酸化调控果蝇卵母细胞极性的形成。

Lgl and its phosphorylation by aPKC regulate oocyte polarity formation in Drosophila.

作者信息

Tian Ai-Guo, Deng Wu-Min

机构信息

Department of Biological Science, Florida State University, Tallahassee, FL 32306-4370, USA.

出版信息

Development. 2008 Feb;135(3):463-71. doi: 10.1242/dev.016253. Epub 2007 Dec 19.

Abstract

Specification of the anteroposterior (AP) axis in Drosophila oocytes requires proper organization of the microtubule and actin cytoskeleton. The establishment and regulation of cytoskeletal polarity remain poorly understood, however. Here, we show important roles for the tumor suppressor Lethal (2) giant larvae (Lgl) and atypical protein kinase C (aPKC) in regulating microtubule polarity and setting up the AP axis of the oocyte. Lgl in the germline cells regulates the localization of axis-specifying morphogens. aPKC phosphorylation of Lgl restricts Lgl activity to the oocyte posterior, thereby dividing the cortex into different domains along the AP axis. Active Lgl promotes the formation of actin-rich projections at the oocyte cortex and the posterior enrichment of the serine/threonine kinase Par-1, a key step for oocyte polarization. Our studies suggest that Lgl and its phosphorylation by aPKC may form a conserved regulatory circuitry in polarization of various cell types.

摘要

果蝇卵母细胞前后轴(AP轴)的特化需要微管和肌动蛋白细胞骨架的适当组织。然而,细胞骨架极性的建立和调控仍知之甚少。在这里,我们展示了肿瘤抑制因子致死(2)巨幼虫(Lgl)和非典型蛋白激酶C(aPKC)在调节微管极性和建立卵母细胞AP轴方面的重要作用。生殖系细胞中的Lgl调节轴特异性形态发生素的定位。aPKC对Lgl的磷酸化将Lgl的活性限制在卵母细胞后部,从而沿AP轴将皮质分为不同区域。活性Lgl促进卵母细胞皮质富含肌动蛋白的突起的形成以及丝氨酸/苏氨酸激酶Par-1在后部的富集,这是卵母细胞极化的关键步骤。我们的研究表明,Lgl及其被aPKC磷酸化可能在各种细胞类型的极化中形成一个保守的调控回路。

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