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目的地:内核膜。

Destination: inner nuclear membrane.

机构信息

Stowers Institute for Medical Research, Kansas City, MO 64110, USA.

Stowers Institute for Medical Research, Kansas City, MO 64110, USA; Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA.

出版信息

Trends Cell Biol. 2014 Apr;24(4):221-9. doi: 10.1016/j.tcb.2013.10.006. Epub 2013 Nov 19.

Abstract

The inner nuclear membrane (INM) of eukaryotic cells is enriched in proteins that are required for nuclear structure, chromosome organization, DNA repair, and transcriptional control. Mislocalization of INM proteins is observed in a wide spectrum of human diseases; however, the mechanism by which INM proteins reach their final destination is poorly understood. In this review we discuss how investigating INM composition, dissecting targeting pathways of conserved INM proteins in multiple systems and analyzing the nuclear transport of viruses and signaling complexes have broadened our knowledge of INM transport to include both nuclear pore complex-dependent and -independent pathways. The study of these INM targeting pathways is important to understanding nuclear organization and in both normal and diseased cells.

摘要

真核细胞的内核膜(INM)富含多种蛋白,这些蛋白对于核结构、染色体组织、DNA 修复和转录调控都是必需的。在广泛的人类疾病中观察到 INM 蛋白的定位错误;然而,INM 蛋白到达其最终目的地的机制还了解甚少。在这篇综述中,我们讨论了如何研究 INM 的组成,在多个系统中剖析保守 INM 蛋白的靶向途径,以及分析病毒和信号复合物的核转运,这些研究拓宽了我们对 INM 转运的认识,包括核孔复合物依赖和非依赖的途径。研究这些 INM 靶向途径对于理解核组织以及正常和病变细胞都很重要。

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