Dicistronic vectors utilizing the internal ribosomal entry site sequen
ce of poliovirus as the intercistronic region were constructed for gen
e expression in mammalian cells. We have developed two monocistronic e
xpression vectors which facilitate the creation of dicistronic express
ion plasmids. The dicistronic expression plasmids encode transcription
units which allow the coordinated translation of the two genes. Using
internal luciferase and secreted alkaline phosphatase, we show the co
rrelated expression of both reporter genes and expression levels compa
rable to those achieved by the respective monocistronic expression vec
tors.