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一种与Ran/TC4结合的巨大核孔蛋白。

A giant nucleopore protein that binds Ran/TC4.

作者信息

Yokoyama N, Hayashi N, Seki T, Panté N, Ohba T, Nishii K, Kuma K, Hayashida T, Miyata T, Aebi U

机构信息

Department of Molecular Biology, Graduate School of Medical Science, Kyushu-University, Fukuoka, Japan.

出版信息

Nature. 1995 Jul 13;376(6536):184-8. doi: 10.1038/376184a0.

Abstract

Ran/TC4 is a small nuclear G protein that forms a complex with the chromatin-bound guanine nucleotide release factor RCC1 (ref. 2). Loss of RCC1 causes defects in cell cycle progression, RNA export and nuclear protein import. Some of these can be suppressed by overexpression of Ran/TC4 (ref. 1), suggesting that Ran/TC4 functions downstream of RCC1. We have searched for proteins that bind Ran/TC4 by using a two-hybrid screen, and here we report the identification of RanBP2, a novel protein of 3,224 residues. This giant protein comprises an amino-terminal 700-residue leucine-rich region, four RanBP1-homologous (refs 9, 10) domains, eight zinc-finger motifs similar to those of NUP153 (refs 11, 12), and a carboxy terminus with high homology to cyclophilin. The molecule contains the XFXFG pentapeptide motif characteristic of nuclear pore complex (NPC) proteins, and immunolocalization suggests that RanBP2 is a constituent of the NPC. The fact that NLS-mediated nuclear import can be inhibited by an antibody directed against RanBP2 supports a functional role in protein import through the NPC.

摘要

Ran/TC4是一种小核G蛋白,它与结合在染色质上的鸟嘌呤核苷酸释放因子RCC1形成复合物(参考文献2)。RCC1的缺失会导致细胞周期进程、RNA输出和核蛋白输入出现缺陷。其中一些缺陷可以通过Ran/TC4的过表达得到抑制(参考文献1),这表明Ran/TC4在RCC1的下游发挥作用。我们通过双杂交筛选寻找与Ran/TC4结合的蛋白质,在此报告鉴定出一种由3224个残基组成的新型蛋白质RanBP2。这种巨大的蛋白质包括一个氨基末端的700个残基的富含亮氨酸区域、四个与RanBP1同源的结构域(参考文献9、10)、八个与NUP153类似的锌指基序(参考文献11、12)以及一个与亲环蛋白具有高度同源性的羧基末端。该分子含有核孔复合体(NPC)蛋白质特有的XFXFG五肽基序,免疫定位表明RanBP2是NPC的一个组成部分。针对RanBP2的抗体能够抑制NLS介导的核输入这一事实,支持了其在通过NPC进行蛋白质输入过程中的功能作用。

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