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Ran的一部分在中心体处与AKAP450相关联:参与微管组织活动。

Part of Ran is associated with AKAP450 at the centrosome: involvement in microtubule-organizing activity.

作者信息

Keryer Guy, Di Fiore Barbara, Celati Claude, Lechtreck Karl Ferdinand, Mogensen Mette, Delouvee Annie, Lavia Patrizia, Bornens Michel, Tassin Anne-Marie

机构信息

Institut Curie, Section Recherche, Unité Mixte Recherche 144-Centre National de la Recherche Scientifique, 75248 Paris, France.

出版信息

Mol Biol Cell. 2003 Oct;14(10):4260-71. doi: 10.1091/mbc.e02-11-0773. Epub 2003 Jul 11.

Abstract

The small Ran GTPase, a key regulator of nucleocytoplasmic transport, is also involved in microtubule assembly and nuclear membrane formation. Herein, we show by immunofluorescence, immunoelectron microscopy, and biochemical analysis that a fraction of Ran is tightly associated with the centrosome throughout the cell cycle. Ran interaction with the centrosome is mediated by the centrosomal matrix A kinase anchoring protein (AKAP450). Accordingly, when AKAP450 is delocalized from the centrosome, Ran is also delocalized, and as a consequence, microtubule regrowth or anchoring is altered, despite the persisting association of gamma-tubulin with the centrosome. Moreover, Ran is recruited to Xenopus sperm centrosome during its activation for microtubule nucleation. We also demonstrate that centrosomal proteins such as centrin and pericentrin, but not gamma-tubulin, AKAP450, or ninein, undertake a nucleocytoplasmic exchange as they concentrate in the nucleus upon export inhibition by leptomycin B. Together, these results suggest a challenging possibility, namely, that centrosome activity could depend upon nucleocytoplasmic exchange of centrosomal proteins and local Ran-dependent concentration at the centrosome.

摘要

小分子Ran GTP酶是核质运输的关键调节因子,也参与微管组装和核膜形成。在此,我们通过免疫荧光、免疫电子显微镜和生化分析表明,在整个细胞周期中,一部分Ran与中心体紧密相关。Ran与中心体的相互作用由中心体基质A激酶锚定蛋白(AKAP450)介导。因此,当AKAP450从中心体上脱离时,Ran也会脱离,结果是,尽管γ-微管蛋白与中心体持续结合,但微管的重新生长或锚定仍会改变。此外,在非洲爪蟾精子中心体激活以进行微管成核时,Ran会被招募到中心体。我们还证明,诸如中心蛋白和中心粒外周蛋白等中心体蛋白,而不是γ-微管蛋白、AKAP450或九蛋白,在被雷帕霉素B抑制输出后集中在细胞核中时会进行核质交换。总之,这些结果提示了一种具有挑战性的可能性,即中心体活性可能取决于中心体蛋白的核质交换以及Ran在中心体处的局部依赖性浓度。

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