We describe here the conditional expression of the hepatitis B virus X prot
ein using the inducible system controlled by a tet-responsive promoter. Ind
uction of the X protein in Rat-2 fibroblasts activated transcription from a
heterologous gene promoter and stimulated the DNA-binding activity of NFkB
. The ability to produce this biologically active X protein in a stable cel
l line will accelerate the elucidation of the function and mechanisms of X
and eventually help us understand the role of X in natural viral infection
and carcinogenesis.