Human foamy virus (HFV) comprises a complex genomic organization of ga
g, pol, env, and several nonstructural genes such as bell, bel2, bel3,
bet, beo, and bes located between env and 3' LTR. Among these viral n
onstructural genes, bell appears to encode an essential transactivator
of LTR-directed gene expression. To investigate the roles of the othe
r nonstructural proteins for the viral replication, a series of provir
al mutants were generated and tested for their in vitro replication. T
he mutations in the other than bell open reading frame did not show an
y significant effect on viral replication. The bell protein is the onl
y essential transactivator for the LTR-directed transcription. To dete
rmine whether HFV has an essential post-transcriptional transactivator
like the rev protein of human immunodeficiency virus type 1, or the r
ex protein of human T cell leukemia virus type 1, we investigated the
bell-independent expression of the HFV gag structural gene under the c
ontrol of the heterologous simian virus 40 promoter. We demonstrated t
hat the expression of the HFV gag structural gene does not require an
essential post-transcriptional transactivator. Thus, it appears that t
he regulation of HFV gene expression is distinct from that of other hu
man retroviruses. (C) 1994 Academic Press, Inc.