Nuclear pore complexes are the vital communication links that permit t
he regulated movement of macromolecules between the cytoplasm and nucl
eus of a cell. As with many other complex cellular events, much of our
understanding about pore dynamics and function comes from studying sy
stems that faithfully reproduce these processes in vitro. Two systems
have provided the bulk of our knowledge. The first system reconstitute
s nuclear import into permeabilized cultured cells. Import is dependen
t on exogenously added cytosol, and fractionation of this cytosol has
led to the identification and characterization of most of the nuclear
transport factors. The second system uses a nuclear reconstitution sys
tem derived from Xenopus eggs to study transport and to assemble nucle
ar pores from their component parts. This system has allowed the chara
cterization of both individual pore components and distinct steps in t
he pore assembly pathway.