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 ove
rexpression of Ran/TC4 (ref. 1), suggesting that Ran/TC4 functions dow
nstream of RCC1. We have searched for proteins that bind Ran/TC4 by us
ing a two-hybrid screen, and here we report the identification of RanB
P2, a novel protein of 3,224 residues. This giant protein comprises an
amino-terminal 700-residue leucine-rich region, four RanBP1-homologou
s (refs 9, 10) domains, eight zinc-finger motifs similar to those of N
UP153 (refs 11, 12), and a carboxy terminus with high homology to cycl
ophilin(13). The molecule contains the XFXFG pentapeptide motif charac
teristic of nuclear pore complex (NPC) proteins(14), and immunolocaliz
ation suggests that RanBP2 is a constituent of the NPC. The fact that
NLS-mediated nuclear import can be inhibited by an antibody directed a
gainst RanBP2 supports a functional role in protein import through the
NPC.