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磷脂酰肌醇3激酶β通过控制RCC1定位和Ran活性来保护核膜完整性。

Phosphoinositide 3-kinase beta protects nuclear envelope integrity by controlling RCC1 localization and Ran activity.

作者信息

Redondo-Muñoz Javier, Pérez-García Vicente, Rodríguez María J, Valpuesta José M, Carrera Ana C

机构信息

Departments of Immunology and Oncology, Centro Nacional de Biotecnología (CNB-CSIC), Cantoblanco, Madrid, Spain.

Department of Macromolecular Structures, Centro Nacional de Biotecnología (CNB-CSIC), Cantoblanco, Madrid, Spain.

出版信息

Mol Cell Biol. 2015 Jan;35(1):249-63. doi: 10.1128/MCB.01184-14. Epub 2014 Oct 27.

Abstract

The nuclear envelope (NE) forms a barrier between the nucleus and the cytosol that preserves genomic integrity. The nuclear lamina and nuclear pore complexes (NPCs) are NE components that regulate nuclear events through interaction with other proteins and DNA. Defects in the nuclear lamina are associated with the development of laminopathies. As cells depleted of phosphoinositide 3-kinase beta (PI3Kβ) showed an aberrant nuclear morphology, we studied the contribution of PI3Kβ to maintenance of NE integrity. pik3cb depletion reduced the nuclear membrane tension, triggered formation of areas of lipid bilayer/lamina discontinuity, and impaired NPC assembly. We show that one mechanism for PI3Kβ regulation of NE/NPC integrity is its association with RCC1 (regulator of chromosome condensation 1), the activator of nuclear Ran GTPase. PI3Kβ controls RCC1 binding to chromatin and, in turn, Ran activation. These findings suggest that PI3Kβ regulates the nuclear envelope through upstream regulation of RCC1 and Ran.

摘要

核膜(NE)在细胞核与细胞质之间形成一道屏障,保护基因组的完整性。核纤层和核孔复合体(NPC)是核膜的组成部分,它们通过与其他蛋白质和DNA相互作用来调节核内事件。核纤层的缺陷与核纤层病的发生有关。由于缺乏磷酸肌醇3激酶β(PI3Kβ)的细胞表现出异常的核形态,我们研究了PI3Kβ对维持核膜完整性的作用。敲除pik3cb会降低核膜张力,引发脂质双层/核纤层连续性区域的形成,并损害NPC组装。我们发现PI3Kβ调节核膜/NPC完整性的一种机制是它与染色体凝聚调节因子1(RCC1)(核Ran GTP酶的激活剂)的结合。PI3Kβ控制RCC1与染色质的结合,进而控制Ran的激活。这些发现表明,PI3Kβ通过对RCC1和Ran的上游调节来调控核膜。

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