The transmission of milk-borne or exogenous mouse mammary tumor virus
(MMTV) requires infection of B cells in the gut-associated lymphoid ti
ssue and expression of the superantigen (Sag) protein at the B-cell su
rface. Presentation of Sag at the B-cell surface is required for the t
ransmission of MMTV to T cells and subsequent infection of the target
mammary gland tissue. Because several different promoters have been re
ported for MMTV sag mRNA expression, we investigated whether the detec
tion of spliced sag RNAs was dependent upon the cell type infected or
the particular MMTV strain examined. In this study, we detected expres
sion of spliced sag RNA from the standard promoter and from an interna
l U3 promoter in B-cell lines expressing endogenous Mtv-6 by RT-PCR, a
lthough expression from the standard promoter appeared to be at least
10-fold higher than that observed from the internal U3 promoter. Sag R
NA originating from exogenous C3H MMTV was not observed from either of
the U3 promoters in any cell type examined. However, spliced mRNAs co
ntaining the exogenous C3H MMTV, endogenous Mtv-8 or endogenous Mtv-17
sag genes could be detected from a previously described promoter in t
he envelope coding region regardless of the cell type infected. Becaus
e sag-specific RNAs can be initiated independently of the LTR promoter
s, there may be selection for independent control of MMTV sag and stru
ctural gene expression. (C) 1997 Academic Press.