A GIANT NUCLEOPORE PROTEIN THAT BINDS RAN/TC4

被引:433
作者
YOKOYAMA, N
HAYASHI, N
SEKI, T
PANTE, N
OHBA, T
NISHII, K
KUMA, K
HAYASHIDA, T
MIYATA, T
AEBI, U
FUKUI, M
NISHIMOTO, T
机构
[1] KYUSHU UNIV,GRAD SCH MED SCI,DEPT NEUROSURG,HIGASHI KU,FUKUOKA 81282,JAPAN
[2] KYUSHU UNIV,GRAD SCH MED SCI,DEPT ANAT,HIGASHI KU,FUKUOKA 81282,JAPAN
[3] KYOTO UNIV,FAC SCI,DEPT BIOPHYS,SAKYO KU,KYOTO 606,JAPAN
[4] UNIV BASEL,BIOZENTRUM,ME MULLER INST MICROSCOPY,CH-4056 BASEL,SWITZERLAND
[5] JOHNS HOPKINS UNIV,SCH MED,DEPT CELL BIOL & ANAT,BALTIMORE,MD 21205
关键词
D O I
10.1038/376184a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
RAN/TC4 is a small nuclear G protein(1) that forms a complex with the chromatin-bound guanine nucleotide release factor RCC1 (ref. 2). Loss of RCC1 causes defects in cell-cycle progression(3,4), RNA export(5-7) and nuclear protein import(8). 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(13). The molecule contains the XFXFG pentapeptide motif characteristic of nuclear pore complex (NPC) proteins(14), 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.
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页码:184 / 188
页数:5
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