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核孔复合体组成的改变调节细胞分化。

A change in nuclear pore complex composition regulates cell differentiation.

机构信息

Salk Institute for Biological Studies, Molecular and Cell Biology Laboratory, 10010 N. Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Dev Cell. 2012 Feb 14;22(2):446-58. doi: 10.1016/j.devcel.2011.11.021. Epub 2012 Jan 19.

Abstract

Nuclear pore complexes (NPCs) are built from ∼30 different proteins called nucleoporins or Nups. Previous studies have shown that several Nups exhibit cell-type-specific expression and that mutations in NPC components result in tissue-specific diseases. Here we show that a specific change in NPC composition is required for both myogenic and neuronal differentiation. The transmembrane nucleoporin Nup210 is absent in proliferating myoblasts and embryonic stem cells (ESCs) but becomes expressed and incorporated into NPCs during cell differentiation. Preventing Nup210 production by RNAi blocks myogenesis and the differentiation of ESCs into neuroprogenitors. We found that the addition of Nup210 to NPCs does not affect nuclear transport but is required for the induction of genes that are essential for cell differentiation. Our results identify a single change in NPC composition as an essential step in cell differentiation and establish a role for Nup210 in gene expression regulation and cell fate determination.

摘要

核孔复合体(NPC)由约 30 种不同的蛋白质组成,这些蛋白质被称为核孔蛋白或 Nups。先前的研究表明,几种 Nups 表现出细胞类型特异性表达,并且 NPC 成分的突变导致组织特异性疾病。在这里,我们表明 NPC 组成的特定变化对于肌原性和神经元分化都是必需的。跨膜核孔蛋白 Nup210 在增殖的成肌细胞和胚胎干细胞(ESCs)中不存在,但在细胞分化过程中表达并整合到 NPC 中。通过 RNAi 阻止 Nup210 的产生会阻止成肌细胞的形成和 ESCs 分化为神经祖细胞。我们发现,将 Nup210 添加到 NPC 中不会影响核转运,但对于诱导对细胞分化至关重要的基因是必需的。我们的结果确定 NPC 组成的单一变化是细胞分化的一个必要步骤,并确立了 Nup210 在基因表达调控和细胞命运决定中的作用。

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