Complementary DNA clones encoding the murine homolog (mCAR) of the hum
an coxsackievirus and adenovirus receptor (CAR) were isolated. Nonperm
issive CHO cells transfected with mCAR cDNA became susceptible to infe
ction by coxsackieviruses B3 and B4 and showed increased susceptibilit
y to adenovirus-mediated gene transfer. These results indicate that th
e same receptor is responsible for virus interactions with both murine
and human cells. Analysis of receptor expression in human and murine
tissues should be useful in defining factors governing virus tropism i
n vivo.