首页> 外文期刊>Nucleus >Comparative ultrastructure of CRM1-Nucleolar bodies (CNoBs), Intranucleolar bodies (INBs) and hybrid PML/p62 bodies uncovers new facets of nuclear body dynamic and diversity
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Comparative ultrastructure of CRM1-Nucleolar bodies (CNoBs), Intranucleolar bodies (INBs) and hybrid PML/p62 bodies uncovers new facets of nuclear body dynamic and diversity

机译:CRM1-核仁体(CNoBs),核仁体内(INBs)和PML / p62杂合体的比较超微结构揭示了核体动态和多样性的新方面

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In order to gain insights on the nuclear organization in mammalian cells, we characterized ultrastructurally nuclear bodies (NBs) previously described as fluorescent foci. Using high resolution immunoelectron microscopy (I-EM), we provide evidence that CNoBs (CRM1-Nucleolar bodies) and INBs (Intranucleolar bodies) are distinct genuine nucleolar structures in untreated HeLa cells. INBs are fibrillar and concentrate the post-translational modifiers SUMO1 and SUMO-2/3 as strongly as PML bodies. In contrast, the smallest CRM1-labeled CNoBs are vitreous, preferentially located at the periphery of the nucleolus and, intricately linked to the chromatin network. Upon blockage of the CRM1-dependent nuclear export by leptomycin B (LMB), CNoBs disappear while p62/SQSTM1-containing fibrillar nuclear bodies are induced. These p62 bodies are enriched in ubiquitinated proteins. They progressively associate with PML bodies to form hybrid bodies of which PML decorates the periphery while p62/SQSTM1 is centrally-located. Our study is expanding the repertoire of nuclear bodies; revealing a previously unrecognized composite nucleolar landscape and a new mode of interactions between ubiquitous (PML) and stress-induced (p62) nuclear bodies, resulting in the formation of hybrid bodies.
机译:为了获得关于哺乳动物细胞中核组织的见解,我们对先前称为荧光灶的超微结构核体(NBs)进行了表征。使用高分辨率免疫电子显微镜(I-EM),我们提供证据表明CNoBs(CRM1-核仁体)和INBs(核仁内体)是未经处理的HeLa细胞中独特的真正核仁结构。 INB是原纤维状的,并且浓缩后翻译修饰符SUMO1和SUMO-2 / 3的强度与PML体一样强。相反,最小的CRM1标记的CNoB是玻璃质的,优先位于核仁的外围,并与染色质网络错综复杂地相连。瘦蛋白B(LMB)阻止CRM1依赖的核出口后,CNoB消失,同时诱导了含有p62 / SQSTM1的原纤维核。这些p62体富含泛素化蛋白。它们逐渐与PML主体关联以形成混合主体,其中pML装饰外围,而p62 / SQSTM1位于中央。我们的研究正在扩大核机构的范围。揭示了以前无法识别的复合核仁景观以及无处不在(PML)和应力诱导(p62)核体之间相互作用的新模式,从而导致了杂化体的形成。

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