Transport of macromolecules across the nuclear envelope is an essentia
l activity in eukaryotic cells. RNA molecules within cells are found c
omplexed with proteins and the bound proteins likely contain signals f
or RNA export. RNAs microinjected into Xenopus oocyte nuclei are readi
ly exported, and their export can be competed by self RNA but not by R
NAs of other classes. This indicates that the rate-limiting step in RN
A export is the interaction of RNAs with class-specific proteins, at l
east when substrate RNAs are present at saturating levels. Export of h
ost mRNAs is inhibited following infection try some animal viruses, wh
ile the export of viral RNAs occurs. The HIV-1 RNA-binding protein, Re
v, mediates the export of intron-containing viral RNAs that would norm
ally be retained in nuclei. This requires a nuclear export signal (NES
) within Rev and an element within the RNA to which Rev binds. In yeas
t, heat shock causes accumulation of poly(A)(+) RNA within nuclei but
heat-shock mRNAs are transcribed and exported efficiently. This requir
es elements within heat shock mRNA that probably interact with a cellu
lar protein to facilitate RNA export. In these cases, the proteins tha
t recognize critical sequences in the RNAs probably direct the RNAs to
an RNA export pathway not generally used for mRNA export. This would
circumvent the general retention of most poly(A)(+) mRNAs following he
at shock in yeast and the need for complete splicing of viral mRNAs th
at travel through the normal mRNA export pathway.