A striking property of nuclear pore complexes is their ability to medi
ate bi-directional nucleocytoplasmic traffic of proteins and RNAs. In
the past year, several new nuclear pore proteins have been identified,
but their precise functions remain to be established. Cytosolic facto
rs responsible for the recognition and docking of substrates for nucle
ar transport are also being characterized. It appears that different f
actors are required for the import of karyophilic proteins versus smal
l nuclear ribonucleoprotein particles. Furthermore, the GTPase Ran/TC4
has been shown to play a key role in translocation across the nuclear
pore complex. Specific RNAs require different sets of factors for the
ir export from the nucleus, although a common export route appears to
be utilized by different RNA species. In contrast, nuclear retention h
as been found to have an influence in controlling the rate of protein
exit from the nucleus.