Studies of defective interfering (DI) RNAs of the murine coronavirus m
ouse hepatitis virus (MHV) suggest that a 69-nucleotide-long packaging
signal is necessary for MHV genomic RNA packaging into MHV particles.
In this study we showed that when RNA transcripts that consisted of a
non-MHV sequence and the packaging signal were expressed in MHV-infec
ted cells, they were packaged into MHV particles. Those RNA transcript
s that lacked the packaging signal or those containing a mutated packa
ging signal did not package efficiently. Thus, the presence of the pac
kaging signal was sufficient for RNA packaging into MHV particles.