Epstein-Barr virus (EBV) recombinants with the BamHI C promoter (Cp) d
eleted were compared with wild-type Cp recombinants derived in paralle
l for their ability to initiate and maintain latent Infection and grow
th transformation in primary human B lymphocytes. Cp-deleted recombina
nts infected, transformed, and immortalized B lymphocytes in vitro as
efficiently as wild-type Cp recombinant EBV. Lymphoblastoid cell lines
(LCLs) infected with the Cp-deleted recombinant were indistinguishabl
e from wild-type recombinant-infected LCLs in latent gene expression,
growth rate, morphology, and surface phenotype. Deletion of Cp did not
affect episomal maintenance or spontaneous entry of the virus into ly
tic cycle. The effect of steroid hormones on latent and lytic gene exp
ression on Cp-deleted recombinants was analyzed and shown to be indepe
ndent of the glucocorticoid response element located 5' to Cp. The Bam
HI W promoter, Wp, is used to transcribe EBNA genes in Cp-deleted EBV-
infected cells. Wp is sufficient for growth transformation and mainten
ance of the lymphoblastoid phenotype of EBV-infected lymphocytes in vi
tro. (C) 1995 Academic Press, Inc.